METHODS OF MODULATING IL-22 AND IL-17
CROSS REFERENCE TO RELATED APPLICATIONS
[0001] The present application claims the benefit of United States provisional
application No. 60/814,573, filed June 19, 2006, the entire disclosure of which is
relied upon and incorporated by reference.
TECHNICAL FIELD
[0002] This invention relates to methods of modulating immune responses by
using IL-22 in combination with at least one of IL-17A, IL-17F, or IL-23 or by using an
IL-22 antagonist, such as an antibody or a soluble receptor or a binding protein, in
combination with an antagonist of at least one of IL-17A, IL-17F, or IL-23.
BACKGROUND
[0003] The role of CD4 T cells in regulating immune responses and disease is
well established, lnterleukin-22 (IL-22) is a class II cytokine that is up-regulated in T
cells by IL-9 or ConA (Dumoutier et al., Proc. Natl. Acad. Sci. USA (2000)
97(18):10144-49). One function of IL-22 is to enhance the innate immunity of
peripheral tissues by inducing the expression of anti-microbial peptides including
beta-defensin 2 (hBD-2), S100A7, S100A8, and S100A9 (Wolk et al., Immunity
(2004) 21:241-54; Boniface et al., J. Immunol. (2005) 174:3695-3702). Other studies
have shown that expression of IL-22 mRNA is induced in vivo in response to LPS
administration, and that IL-22 modulates parameters indicative of an acute phase
response (Dumoutier L. et al. (2000); Pittman et al., Genes and Immunity, (2001)
2:172). Taken together, these observations indicate that IL-22 plays a role in
inflammation (Kotenko S.V., Cytokine & Growth Factor Reviews (2002) 13(3):223-
40). Several T cell disorders, including psoriasis (Wolk et al., Immunity (2004)
21:241-54), rheumatoid arthritis (Ikeuchi H. et al. Arthritis Rheum 52:1037-1046),
and inflammatory bowel disease (Andoh, A. et al. Gastroenterology 129:969-984)
are associated with increased levels of IL-22.
[0004] Recent data have demonstrated the existence of a new CD4+ effector
lineage that is defined by its ability to express IL-17A and IL-17F (hereafter referred
to as the Th17 lineage) (Aggarwal et al., J. Biol. Chem., (2003) 278:1910-14;
Langrish et al., J. Exp. Med., (2005) 201:233-40; Harrington et al., Nat. Immunol.,
(2005) 6:1123-32; Park et al., Nat. Immunol., (2005) 6:1133-41; Veldhoen et al.,
Immunity, (2006) 24:179-89; Mangan et al., Nature, (2006) 441:231-34; Bettelli et al.,
Nature, (2006) 441:235-38). Th17 cell differentiation is initiated by TGF-ß signaling
in the context of pro-inflammatory cytokines, particularly IL-6, and also IL-1ß and
TNF-a. Maintenance and survival of Th17 cells, in contrast, are dependent upon IL-
23, an IL-12 family member composed of IL-12p40 and IL-23p19 subunits. IL-23
deficient mice produce significantly less IL-17 in several murine disease and
infection models (Langrish et al., J. Exp. Med., (2005) 201:233-40; Murphy et al., J.
Exp. Med., (2003) 198:1951-57; Happel et al., J. Exp. Med., (2005) 202:761-69;
Khader et al., J. Immunol., (2005) 175:788-95). Thus, Th17 differentiation is initiated
by TGF-|i and pro-inflammatory cytokines and subsequently maintained by IL-23.
[0005] The IL-17 family is composed of five family members — IL-17A, IL-
17B, IL-17C, IL-17D, IL-17E (IL-25), and IL-17F —that share a relative homology
between 17 to 55% (Aggarwal et al., Cytokine Growth Factor Rev., (2003) 14:155-
74; Kolls et al., Immunity, (2004) 21:467-76). The expression of IL-17 family
members is quite diverse. IL-17A and IL-17F are the most homologous (55%) and
are located adjacent to each other on human chromosome 1. IL-17A and IL-17F
mRNA are expressed at higher levels in Th17 cells as compared to Th1 or Th2 cells.
In contrast, IL-17B, IL-17C, and IL-17D are expressed predominantly in non-
lymphoid tissues. IL-17E (IL-25) is expressed in Th2 cells (Fort et al., Immunity,
(2001) 15:985-95). In addition to IL-17A and IL-17F, TNF-a, IL-6, and GM-CSF have
also been identified as genes induced by IL-23 and potentially expressed by Th17
cells (Langrish et al., J. Exp. Med., (2005) 201:233-40; Infante-Duarte et al., J.
Immunol., (2000) 165:6107-15). However, because Th1 cells can express TNF-a
and Th2 cells can express IL-6 and GM-CSF, the expression of IL-6, TNF-a, and
GM-CSF is not restricted to the Th17 lineage. In contrast, Th17 cells are thought to
produce IL-17A and IL-17F in a lineage specific manner.
[0006] Subsets of CD4 effector cells are involved in a number of different
diseases. In some cases, their activity is helpful to the organism. In other diseases,
however, their activity is undesirable or even harmful. Identification of those subsets
of cells within the CD4 effector population that are responsible for a particular
pathology permits targeted regulation of those cells without unneeded suppression of
other CD4 effector cells. Similarly, knowledge of the cytokines produced by cellular
subsets and how those cytokines interact is a prerequisite for the development of
comprehensive therapies that provide improved management of diseases involving
those cytokines. A need therefore exists in the art for further characterization of the
cytokines produced by the Th17 lineage of CD4 effector cells.
[0007] The present application meets this need by showing that IL-22, an IL-
10 family member originally described as a Th1 cytokine, is also a Th17 cytokine that
can act cooperatively, and in some cases, synergistically, with IL-17A or IL-17F. In
addition, IL-22 induction by IL-23 is demonstrated.
SUMMARY
[0008] The present application provides methods of modulating immune
responses by using interleukin-22 ("IL-22") in combination with at least one of
interleukin-17A ("IL-17A"), interleukin-17F ("IL-17F), or interleukin-23 ("IL-23") or by
using an IL-22 antagonist, such as an antibody or a soluble receptor or a binding
protein, in combination with an antagonist of at least one of IL-17A, IL-17F, or IL-23.
[0009] In one embodiment, the methods comprise diagnosing, preventing,
and/or treating diseases associated with IL-22 and least one of IL-17A, IL-17F, or IL-
23. This can be accomplished, at least in part, through the use of compositions
comprising two or more antagonists, such as antibodies, soluble receptors, or
binding proteins, that inhibit IL-22 and at least one of IL-17A, IL-17F, or IL-23.
[0010] The compositions and combinations of antagonists used for preventing
and/or treating diseases decrease the activity of IL-22 and at least one of IL-17A, IL-
17F, or IL-23. For example, the activity of any cytokine can be reduced or inhibited
by contacting it with a composition comprising an antibody that binds to the cytokine
and inhibits its function. The functional activity of a cytokine can also be affected by
reducing or inhibiting its signaling through cellular receptors using agents, such as
antibodies or soluble receptors, that inhibit or reduce signaling through a cytokine
receptor.
[0011] The application also provides methods of stimulating an immune
response by administering IL-22 and at least one of IL-17A, IL-17F, or IL-23.
Stimulation of an immune response may be desirable, for example, when a mammal
is infected by a pathogen, such as a bacterium or virus, or when immunogens are
administered to a mammal as part of a vaccine. Thus, in one embodiment, the
application provides a method of inducing the expression of an anti-microbial peptide
in a cell, such as a keratinocyte, comprising administering IL-22 and IL-17A, IL-22
and IL-17F, IL-22 and IL-23, or IL-22, IL-17A, and IL-17F to the cell. The anti-
microbial peptide can be, for example, a member of the beta-defensin family,
including human beta-defensin 1 or human beta-defensin 2, a member of the S100
family of calcium binding proteins, including S100A7, S100A8, or S100A9, a
cathelicidin, including human cathelicidin LL-37 (see Lee et al., PNAS (2005)
102:3750-55), or a combination thereof. Other embodiments are directed to
methods of inducing an anti-microbial peptide, comprising administering to a
mammal, such as a human, IL-22 and IL-17A, IL-22 and IL-17F, or IL-22, IL-17A,
and IL-17F in amounts effective to induce the anti-microbial peptide in the mammal.
Still other embodiments are directed to methods of inhibiting or reducing the
expression of an anti-microbial peptide in a cell, such as a keratinocyte, comprising
administering an antagonist of IL-22, or an antagonist of IL-22 and an antagonist of
IL-17A, an antagonist of IL-22 and an antagonist IL-17F, or an antagonist of IL-22,
an antagonist of IL-17A, and an antagonist of IL-17F to the cell. Another
embodiment is directed to a method of inhibiting or reducing the expression of an
anti-microbial peptide, comprising administering to a mammal, such as a human, an
antagonist of IL-22, or an antagonist of IL-22 and an antagonist of IL-17A, an
antagonist of IL-22 and an antagonist IL-17F, or an antagonist of IL-22, an
antagonist of IL-17A, and an antagonist of IL-17F in amounts effective to inhibit or
reduce the expression of the anti-microbial peptide. In another embodiment, IL-22
and at least one of IL-17A, IL-17F, or IL-23, are used as an adjuvant. For example,
the adjuvants can comprise IL-22 and IL-17A, IL-22 and IL-17F, IL-22 and IL-23, or
IL-22, IL-17A, and IL-17F. Immunogens of interest in a vaccine can be, for example,
viral, bacterial, or tumor antigens. This application also provides kits comprising the
adjuvants discussed herein, either alone, or combined with an immunogen.
[0012] Compositions used for diagnosing diseases associated with IL-22 and
at least one of IL-17A, IL-17F, or IL-23 need only detect the cytokine proteins or
nucleic acids expressing the cytokines. Antibodies and soluble receptors are
examples of agents that can be used in compositions to detect cytokine proteins.
The nucleic acid expressing a cytokine protein can be detected by a variety of
standard techniques, such as polymerase chain reaction (PCR).
[0013] In one aspect, the method comprises treating a subject with a disorder
associated with IL-22 and at least one of IL-17A, IL-17F, or IL-23. The methods
include administering to the subject a composition in an amount sufficient to reduce
or inhibit the activity of IL-22 and at least one of IL-17A, IL-17F, or IL-23, thereby
treating the disorder. In some embodiments, the composition comprises an IL-22
antagonist, and an antagonist of at least one of IL-17A, IL-17F, or IL-23. In still other
embodiments, the composition comprises a combination of one or more antibodies
and one or more soluble receptors or binding proteins.
[0014] Antagonists that can be used in the invention include antibodies;
soluble receptors, including truncated receptors, natural soluble receptors, or fusion
proteins comprising a receptor (or a fragment thereof) fused to a second protein,
such as an Fc portion of an immunoglobulin; peptide inhibitors; small molecules;
ligand fusions; and binding proteins. Examples of binding proteins include the
naturally-occurring IL-22 binding proteins (or fragments thereof) described in
US2003/0170839, the contents of which are incorporated by reference in its entirety.
Small Modular Immunopharmaceutical (SMIP™) (Trubion Pharmaceuticals, Seattle,
WA) provide an example of a variant molecule comprising a binding domain
polypeptide. SMIPs and their uses and applications are disclosed in, e.g., U.S.
Published Patent Application. Nos. 2003/0118592, 2003/0133939, 2004/0058445,
2005/0136049, 2005/0175614, 2005/0180970, 2005/0186216, 2005/0202012,
2005/0202023, 2005/0202028, 2005/0202534, and 2005/0238646, and related
patent family members thereof, all of which are hereby incorporated by reference
herein in their entireties.
[0015] A SMIP™ typically refers to a binding domain-immunoglobulin fusion
protein that includes a binding domain polypeptide that is fused or otherwise
connected to an immunoglobulin hinge or hinge-acting region polypeptide, which in
turn is fused or otherwise connected to a region comprising one or more native or
engineered constant regions from an immunoglobulin heavy chain, other than CH1,
for example, the CH2 and CH3 regions of IgG and IgA, or the CH3 and CH4 regions
of IgE (see e.g., U.S. 2005/0136049 by Ledbetter, J. et al., which is incorporated by
reference, for a more complete description). The binding domain-immunoglobulin
fusion protein can further include a region that includes a native or engineered
immunoglobulin heavy chain CH2 constant region polypeptide (or CH3 in the case of
a construct derived in whole or in part from IgE) that is fused or otherwise connected
to the hinge region polypeptide and a native or engineered immunoglobulin heavy
chain CH3 constant region polypeptide (or CH4 in the case of a construct derived in
whole or in part from IgE) that is fused or otherwise connected to the CH2 constant
region polypeptide (or CH3 in the case of a construct derived in whole or in part from
IgE). Typically, such binding domain-immunoglobulin fusion proteins are capable of
at least one immunological activity selected from the group consisting of antibody
dependent cell-mediated cytotoxicity, complement fixation, and/or binding to a target,
for example, a target antigen, such as human IL-22, IL-17A, IL-17F, or IL-23.
[0016] In one embodiment, the antagonist is a VHH molecule (or nanobody),
which, as known to the skilled artisan, is a heavy chain variable domain derived from
immunoglobulins naturally devoid of light chains, such as those derived from
Camelidae as described in WO 9404678 and U.S. Patent No. 5,759,808, both of
which are incorporated herein by reference. Such a VHH molecule can be derived
from antibodies raised in Camelidae species, for example in camel, llama,
dromedary, alpaca and guanaco and is sometimes called a camelid or camelized
variable domain. See e.g., Muyldermans., J. Biotechnology (2001) 74(4):277-302,
incorporated herein by reference. Other species besides Camelidae may produce
heavy chain antibodies naturally devoid of light chain. VHH molecules are about 10
times smaller than IgG molecules. They are single polypeptides and very stable,
resisting extreme pH and temperature conditions. Moreover, they are resistant to
the action of proteases which is not the case for conventional antibodies.
Furthermore, in vitro expression of VHHs produces high yield, properly folded
functional VHHs. In addition, antibodies generated in Camelids will recognize
epitopes other than those recognized by antibodies generated in vitro through the
use of antibody libraries or via immunization of mammals other than Camelids (see
WO 9749805 and U.S. Patent Application Publication 2004/0248201, both of which
are incorporated herein by reference).
[0017] Thus, in one embodiment, the composition comprises a first antibody
that binds to IL-22 and a second antibody that binds to either IL-17A, IL-17F, or IL-
23. In another embodiment, the composition comprises an antibody that binds to IL-
22 and a soluble receptor (or binding protein) that binds to IL-17A, IL-17F, or IL-23.
In yet another embodiment, the composition comprises a soluble receptor that binds
to IL-22 and an antibody or soluble receptor (or binding protein) that bind to IL-17A,
IL-17F, or IL-23. In a further embodiment, the composition comprises an IL-22
binding protein and an antibody or soluble receptor (or binding protein) that binds to
IL-17A, IL-17F, or IL-23.
[0018] The compositions can be administered to the subject, either alone or in
combination with additional therapeutic agents as described herein. The subject
may be a mammal, e.g. human. In some embodiments, the composition is
administered locally, e.g., topically, subcutaneously, or other administrations that are
not in the general circulation. In other embodiments, the composition is administered
to the general circulation, for example, by intravenous (i.v.) or subcutaneous (s.c.)
administration. The different agonists and antagonists may be administered
simultaneously or sequentially.
[0019] Examples of disorders associated with one or more of IL-22, IL-17A, IL-
17F, or IL-23 include respiratory disorders, inflammatory disorders, and autoimmune
disorders. In particular, disorders associated with one or more of IL-22, IL-17A, IL-
17F, or IL-23 include arthritis (including rheumatoid arthritis, juvenile rheumatoid
arthritis, osteoarthritis, psoriatic arthritis, lupus-associated arthritis or ankylosing
spondylitis), scleroderma, systemic lupus erythematosis, vasculitis, multiple
sclerosis, autoimmune thyroiditis, dermatitis (including atopic dermatitis and
eczematous dermatitis), myasthenia gravis, inflammatory bowel disease (IBD),
Crohn's disease, colitis, diabetes mellitus (type I); inflammatory conditions of, e.g.,
the skin (e.g., psoriasis), cardiovascular system (e.g., atherosclerosis), nervous
system (e.g., Alzheimer's disease), liver (e.g., hepatitis), kidney (e.g., nephritis) and
pancreas (e.g., pancreatitis); cardiovascular disorders, e.g., cholesterol metabolic
disorders, oxygen free radical injury, ischemia; disorders associated with wound
healing; respiratory disorders, e.g., asthma and COPD (e.g., cystic fibrosis); acute
inflammatory conditions (e.g., endotoxemia, septicemia, toxic shock syndrome and
infectious disease); transplant rejection and allergy.
[0020] In yet another aspect, the application provides methods of treating
psoriasis by administering to a psoriasis patient a composition comprising an IL-17F
antagonist, such as an antibody or a soluble receptor in therapeutically effective
amounts. The IL-17F antagonist may be administered alone or in combination with
an IL-22 antagonist, such as an antibody, soluble receptor, or binding protein.
[0021] In another aspect, the application provides a method for detecting the
presence of IL-22 and at least one of IL-17A, IL-17F, or IL-23 in a sample in vitro.
Samples may include biological materials such as blood, serum, plasma, tissue,
biopsy, and bronchoalveolar lavage. The subject method can be used to diagnose a
disorder, such as a disorder associated with one or more of IL-22, IL-17A, IL-17F, or
IL-23, as described in this application. Such a method can include: (1) contacting
the sample or a control sample with a first reagent that binds to IL-22 and a second
reagent that binds to IL-17A, IL-17F, or IL-23, and (2) detecting formation of a
complex between the first and second reagents and the sample or the control
sample, wherein a statistically significant change in the formation of the complex in
the sample relative to a control sample, is indicative of the presence of the cytokines
in the sample. In one embodiment, the method includes contacting a sample
comprising cells with a labeled regeant, such as a fluorescent antibody, that binds to
IL-22, IL-17A, IL-17F, or IL-23 within the cells. The amount of reagent detected
within a cell is proportional to the amount of intracellular IL-22, IL-17A, IL-17F, or IL-
23 expressed within the cell.
[0022] In yet another aspect, the application provides an in vivo detection
method (e.g., in vivo imaging in a subject). The method can be used to diagnose a
disorder, including those disorders described in this application. Such a method can
include: (1) administering a first reagent that binds to IL-22 and a second reagent
that binds to IL-17A, IL-17F, or IL-23 to a subject or a control subject under
conditions that allow binding of the first and second reagents to their cytokines, and
(2) detecting formation of a complex between the first and second reagents and their
cytokines, wherein a statistically significant change in the formation of the complex in
the subject relative to a control, e.g., a control subject, is indicative of the presence
of the cytokines.
[0023] Examples of reagents that bind to cytokines used in the methods of the
invention include antibodies, soluble receptors, and binding proteins. These
reagents may be directly or indirectly labeled with a detectable substance to facilitate
detection. Suitable detectable substances include various enzymes, prosthetic
groups, fluorescent materials, luminescent materials and radioactive materials.
[0024] Additional aspects of the disclosure will be set forth in part in the
description, and in part will be obvious from the description, or may be learned by
practicing the invention. Certain embodiments are set forth and particularly pointed
out in the claims, and the disclosure should not be construed as limiting the scope of
the claims. The following detailed description includes exemplary representations of
various embodiments, which are not restrictive of the subject matter claimed. The
accompanying figures constitute a part of this specification and, together with the
description, serve only to illustrate embodiments and not limit the invention.
BRIEF DESCRIPTION OF THE FIGURES
[0025] Figure 1. Cytokine transcript expression profiles for Th1, Th2 and
Th17 cells. (A) Quantitative PCR analysis of relative cytokine expression in cells
induced to differentiate into Th1, Th2, and Th17 cells. (B) Relative IL-22 levels
induced in Th1, Th2, and Th17 cells. (C) Relative levels of IL-2, IL-3, IL-5, IL-6, IL-9,
IL-10, IL-13, IL-21, IL-24, IL-25, and IL-31 in Th1, Th2, and Th17 cells. (D) Relative
levels of IL-1, IL-7, IL-11, IL-15, IL-16, IL-18, IL-19, IL-20, IL-27, and IL-28 inThl,
Th2, and Th 17 cells.
[0026] Figure 2. Expression levels of IL-22 and IL-17A protein in T cell
subsets. (A) Levels of IL-22, IL-17A and IFN-? protein following activation in the
presence of various cytokines, antibodies, and antigen. (B) IL-22 levels in
differentiated cells restimulated with antigen and various cytokines and antibodies.
[0027] Figure 3. Effects of exogenous IL-22 addition. (A) Levels of IL-22R1
transcripts in the indicated populations following addition of exogneous IL-22. (B)
Proliferation of naive cells in response to exogenous IL-22. (C) IFN-? production by
Th1 cells in response to exogenous IL-22. (D) IL-4 production by Th2 cells in
response to exogenous IL-22. (E) IL-17 production by Th17 cells in response to
exogenous IL-22.
[0028] Figure 4. Intracellular cytokine levels in T cell populations. (A) Flow
cytometric analysis of IL-22 co-expression with IFN-?or IL-17A in Th1, Th2, and
Th17 cells. (B) Flow cytometric analysis of IL-17A and IL-17F co-expression in IL-
22-expressing CD4 cells cultured in the presence of the indicated cytokines. (C)
Effect of anti-TGF-p addition on IL-22 levels.
[0029] Figure 5. Expansion of IL-22-producing cells by IL-23. (A) Intracellular
staining for IL-22 in naive T cells cultured with antigen and the indicated cytokines.
The the graph shows the percentage IL-22 cells in the culture as a function of time
while the dot plots show IL-22 and IL-17A levels on day 2 and day 4. (B) CFSE
profiles on day 4 of cells separated into four populations: IL-22+IL-17A', IL-22+IL-
17A+, IL-22IL-17A+, and IL-22-IL-17A (C) IL-22 expression in naive DO11 T cells
cultured with LPS activated DCs, OVAp, and neutralizing antibodies to either IL-23R
or lL-12p40.
[0030] Figure 6. In vivo expression of IL-22 in the absence of IL-6 or IL-23.
IL-22 expression in C57BL/6 IL-6-/- (A) and C57BL/6 IL-23p19-/- (B) mice following
immunization with OVA. IL-22 expression in wildtype (WT) mice is also shown.
[0031] Figure 7. Flow cytometric and ELISA analysis of in vivo IL-22 co-
expression with IL-17A and IL-17F. (A) LN cells stained for CD4 and IL-22, IL-17A,
IL-17F, or isotype controls. (B) IL-22 expression in relation to IFN-?, IL-17A, IL-17F,
IL-4, and IL-10 in CD4+ T cells. (C) Expression of IL-22 in various IL-17A+ and IL-
17F+ populations. (D) Expression of IL-17A and IL-17F in IL-22+ cells. (E) IL-22 and
IL-17A concentrations as determined on day 4 of restimulation by ELISA.
[0032] Figure 8. Analysis of IL-22 production by human Th17 cells and
human Th1 cells. (A) IL-22 and IL-17A expression following culture of human CD4+
T cells with the indicated cytokines and antibodies. Each line represents an
individual donor. (B) The percentage of Th1 or Th17 cells expressing IL-22 were
calculated for each of the six donors examined in (A). "Th1 cells" (open bars) were
defined by the expression of IFN-?. Th17 cells" (stippled bars) were defined by
expression of IL-17A.
[0033] Figure 9. Effect of TGF-ß on expression of IL-22. (A) IL-22 and IL-17A
expression following culture of human CD4+ T cells with the indicated cytokines and
antibodies. (B) IL-22 expression by naive CD62L+CD4+ T cells from D011.10 mice
activated with 1 µg/ml OVAp, and IL-6. Exogenous TGF-ß cytokine or a neutralizing
antibody to TGF-ß was added as indicated.
[0034] Figure 10. IL-22 induces serum amyloid A (SAA) independently of IL-
6. (A) SAA serum ELISA following IL-22 injection. (B) Quantitative PCR for SAA1,
fibrinogen, haptoglobin, and albumin, normalized to ß2 microglobulin, following
injection of IL-22. (C) Serum IL-6 and TNF-a ELISAs following IL-22 administration.
(D) SAA serum ELISA for C57BL/6 and C57BL/6 IL-6-/- mice administered IL-22.
[0035] Figure 11. Neutrophil numbers and CXCLI levels following IL-22
administration. (A) Neutrophil numbers as determined at the indicated timepoints.
(B) CXCL1 proteins levels in serum. (C) Quantitative PCR of CXCL1 transcripts
levels in the liver.
[0036] Figure 12. Quantitative PCR analysis of IL-22 and IL-17A or IL-17F
induced expression of anti-microbial peptide transcripts. (A) Fold induction of hBD-2,
S100A7, S100A8, and S100A9 transcript in primary human keratinocytes treated
with IL-22, IL-17A, or IL-17F. (B) Fold induction of hBD-2, S100A7, S100A8, and
S100A9 transcript in primary human keratinocytes treated pairwise with
combinations of IL-22, IL-17A, and IL-17F.
[0037] Figure 13. IL-22, IL-17A, IL-17F, and IL-23p19 transcript expression in
lesional skin of psoriasis patients. (A) Quantitative PCR analysis for IL-22, IL-17A,
IL-17F, and IL-23p19. (B) Spearman's rank correlation analysis between IL-22 and
IL-17A, IL-22 and IL-17F, IL-17A and IL-17F, IL-22 and IL-23, IL-23 and IL17A, and
IL-23 and lL-17F.
DETAILED DESCRIPTION
I. Definitions
[0038] In order that the present invention may be more readily understood,
certain terms are first defined. Additional definitions are set forth throughout the
detailed description.
[0039] The term "antibody" refers to an immunoglobulin or fragment thereof,
and encompasses any polypeptide comprising an antigen-binding fragment or an
antigen-binding domain. The term includes but is not limited to polyclonal,
monoclonal, monospecific, polyspecific, non-specific, humanized, human,
single-chain, chimeric, synthetic, recombinant, hybrid, mutated, grafted, and in vitro
generated antibodies. Unless preceded by the word "intact", the term "antibody"
includes antibody fragments such as Fab, F(ab')2, Fv, scFv, Fd, dAb, and other
antibody fragments that retain antigen-binding function. The present invention is not
necessarily limited to any particular source, method of production, or other special
characteristics of an antibody. Further, the antibodies may be tagged with a
detectable or functional label. These labels include radiolabels (e.g., 131l or 99Tc),
enzymatic labels (e.g., horseradish peroxidase or alkaline phosphatase), and other
chemical moieties (e.g., biotin).
[0040] The phrase "inhibit' or "antagonize" cytokine activity and its cognates
refer to a reduction, inhibition, or otherwise diminution of at least one activity of that
cytokine due to binding an anti-cytokine antibody or soluble receptor to the cytokine
or due to competition for binding to the cytokine receptor, wherein the reduction is
relative to the activity of cytokine in the in the absence of the same antibody, soluble
receptor, or competitive inhibitor. The activity can be measured using any technique
known in the art. Inhibition or antagonism does not necessarily indicate a total
elimination of cytokine biological activity. A reduction in activity may be about 10%,
20%, 30%, 40%, 50%, 60%, 70%, 80%, 90%, or more.
[0041] The term "cytokine activity", whether used generally or as applied to
a particular cytokines such as IL-22, IL-17A, IL-17F, or IL-23, refers to at least one
cellular process initiated or interrupted as a result of binding of that cytokine to its
receptor(s) on a cell. Cytokine activities for IL-22 include at least one of, but are not
limited to: (1) binding to a cellular receptor subunit or complex, such as IL-22R1, IL-
10R2, or IL-22R1/IL-10R2; (2) associating with signal transduction molecules (e.g.,
JAK-1); (3) stimulating phosphorylation of STAT proteins (e.g., STAT5, STAT3, or
combination thereof); (4) activating STAT proteins; (5) inducing parameters
indicative of an acute phase response, including the modulation of acute phase
reactants (e.g., serum amyloid A, fibrinogen, haptoglobin, or serum albumin) and
cells (e.g., neutrophils, platelets, or red blood cells; and (6) modulating (e.g.,
increasing or decreasing) proliferation, differentiation, effector cell function, cytolytic
activity, cytokine secretion, survival, or combinations thereof, of epithelial cells,
fibroblasts, or immune cells. Epithelial cells include, but are not limited to, cells of
the skin, gut, liver, and kidney, as well as endothelial cells. Fibroblasts include, but
are not limited to, synovial fibroblasts. Immune cells may include CD8+ and CD4+ T
cells, NK cells, B cells, macrophages, megakaryocytes, and specialized or tissue
immune cells, such as those found in inflammed tissues or those expressing an IL-
22 receptor.
[0042] Cytokine activities for IL-17A and IL-17F include at least one of, but are
not limited to: (1) binding to a cellular receptor, such as IL-17R, IL-17A, IL-17RC, IL-
17RH1, IL-17RL, IL-17RD, or IL-17RE ; (2) inhibition of angiogenesis; (3) modulating
(e.g., increasing or decreasing) proliferation, differentiation, effector cell function,
cytolytic activity, cytokine secretion, survival, or combinations thereof, of
hematopoietic cells or cells present in cartilage, bone, meniscus, brain, kidney, lung,
skin and intestine; (4) inducing production of IL-6 and/or IL-8; and (5) stimulating
nitric oxide production.
[0043] Cytokine activities for IL-23 include at least one of, but are not limited
to: (1) binding to a cellular receptor, such as IL-23R or IL-12R(31, (2) signaling via
Jak2, Tyk2, Statl, Stat3, Stat4, and Stat5; (3) modulating (e.g., increasing or
decreasing) proliferation, differentiation, effector cell function, cytolytic activity,
cytokine secretion, survival, or combinations thereof, of immune cells, such as CD4+
T cells, NK cells, and macrophages; and (4) inducing production of IL-22, IL-17A, or
IL-17F.
[0044] The term "isolated" refers to a molecule that is substantially free of its
natural environment. For instance, an isolated protein is substantially free of cellular
material or other proteins from the cell or tissue source from which it was derived.
The term also refers to preparations where the isolated protein is sufficiently pure for
pharmaceutical compositions; or at least 70-80% (w/w) pure; or at least 80-90%
(w/w) pure; or at least 90-95% pure; or at least 95%, 96%, 97%, 98%, 99%, or 100%
(w/w) pure.
[0045] The terms "specific binding" or "specifically binds" refers to two
molecules forming a complex that is relatively stable under physiologic conditions.
Specific binding is characterized by a high affinity and a low to moderate capacity as
distinguished from nonspecific binding which usually has a low affinity with a
moderate to high capacity. Typically, binding is considered specific when the
association constant KA is higher than 106M-1. If necessary, nonspecific binding can
be reduced without substantially affecting specific binding by varying the binding
conditions. The appropriate binding conditions, such as concentration of antibodies,
ionic strength of the solution, temperature, time allowed for binding, concentration of
a blocking agent (e.g., serum albumin, milk casein), etc., may be optimized by a
skilled artisan using routine techniques.
[0046] The term "therapeutic agent" is a substance that treats or assists in
treating a medical disorder. As used herein, a therapeutic agent refers to a
substance, when administered to a subject along with a composition of the invention,
provides a better treatment compared to administration of the therapeutic agent or
that inventive composition alone. Non-limiting examples and uses of therapeutic
agents are described herein.
[0047] The term "effective amount" refers to a dosage or amount that is
sufficient to regulate cytokine activity to achieve a desired biological outcome, e.g.,
decreased T cell and/or B cell activity, suppression of autoimmunity, suppression of
transplant rejection, suppression of inflammation, systemic or local, etc.
[0048] As used herein, a "therapeutically effective amount" refers to an
amount which is effective, upon single or multiple dose administration to a subject
(such as a human patient) at treating, preventing, curing, delaying, reducing the
severity of, ameliorating at least one symptom of a disorder or recurring disorder, or
prolonging the survival of the subject beyond that expected in the absence of such
treatment.
[0049] The term "treatment" refers to a therapeutic or preventative measure.
The treatment may be administered to a subject having a medical disorder or who
ultimately may acquire the disorder, in order to prevent, cure, delay, reduce the
severity of, or ameliorate one or more symptoms of a disorder or recurring disorder,
or in order to prolong the survival of a subject beyond that expected in the absence
of such treatment.
II. Modulatory Agents
[0050] Various types of agents can be used to regulate or modulate an
immune response that is due in part to the activity of one or more of IL-22, IL-17A,
IL-17F, or IL-23. In some embodiments, the composition comprises an antibody or
antigen-binding fragment thereof that binds to IL-22, an antibody or antigen-binding
fragment thereof that binds to IL-17A, an antibody or antigen-binding fragment
thereof that binds to IL-17F, an antibody or antigen-binding fragment thereof that
binds to IL-23, or a combination of more than one of these antibodies. When the
antibody or antigen-binding fragment thereof binds IL-23, it may bind to an eptiope
present on the p19 subunit of IL-23, an eptiope present on the p40 subunit of IL-23,
or an epitope formed by the combination of the p19 and p40 subunits of IL-23.
[0051] In other embodiments, the composition comprises a soluble receptor of
IL-22, a soluble receptor of IL-17A, a soluble receptor of IL-17F, a soluble receptor of
IL-23, or a combination of these soluble receptors. Examples of soluble receptors
include those in which an immunoglobulin Fc domain has been joined to the
extracellular portion of the receptor.
[0052] In yet other embodiments, the composition comprises a binding protein
that binds to IL-22, IL-17A, IL-17F, or IL-23. Examples of binding proteins that bind
IL-22 include the naturally-occurring IL-22 binding proteins, such as those described
in US2003/0170839, the contents of which are incorporated by reference. When the
binding protein binds IL-23, it may bind at a site on the p19 subunit of IL-23, a site on
the p40 subunit of IL-23, or a site formed by the combination of the p19 and p40
subunits of IL-23.
[0053] In still other embodiments, the composition comprises a combination of
1) one or more antibodies and 2) one or more soluble receptors or binding proteins.
III. Uses of Modulatory Agents
[0054] Compositions that act as agonists or antagonists of one or more of IL-
22, IL-17A, IL-17F, or IL-23 can be used to regulate immune responses caused by
IL-22 and at least one of IL-17A, IL-17F, and IL-23, such as acting on epithelial cells
in solid tissue and indirectly modulating downstream immune responses.
Accordingly, antagonist compositions of the invention can be used directly or
indirectly to inhibit the activity (e.g., proliferation, differentiation, and/or survival) of an
immune or hematopoietic cell (e.g., a cell of myeloid, lymphoid, or erythroid lineage,
or precursor cells thereof), and, thus, can be used to treat a variety of immune
disorders and hyperproliferative disorders. Non-limiting examples of immune
disorders that can be treated include, but are not limited to, autoimmune disorders,
e.g., arthritis (including rheumatoid arthritis, juvenile rheumatoid arthritis,
osteoarthritis, psoriatic arthritis, lupus-associated arthritis or ankylosing spondylitis),
scleroderma, systemic lupus erythematosis, vasculitis, multiple sclerosis,
autoimmune thyroiditis, dermatitis (including atopic dermatitis and eczematous
dermatitis), myasthenia gravis, inflammatory bowel disease (IBD), Crohn's disease,
colitis, diabetes mellitus (type I); inflammatory conditions of, e.g., the skin (e.g.,
psoriasis), cardiovascular system (e.g., atherosclerosis), nervous system (e.g.,
Alzheimer's disease), liver (e.g., hepatitis), kidney (e.g., nephritis) and pancreas
(e.g., pancreatitis); cardiovascular disorders, e.g., cholesterol metabolic disorders,
oxygen free radical injury, ischemia; disorders associated with wound healing;
respiratory disorders, e.g., asthma and COPD (e.g., cystic fibrosis); acute
inflammatory conditions (e.g., endotoxemia, septicemia, toxic shock syndrome and
infectious disease); transplant rejection and allergy. In one embodiment, the
disorder is, an arthritic disorder, e.g., a disorder chosen from one or more of
rheumatoid arthritis, juvenile rheumatoid arthritis, osteoarthritis, psoriatic arthritis, or
ankylosing spondylitis; a respiratory disorder (e.g., asthma, chronic obstructive
pulmonary disease (COPD); or an inflammatory condition of, e.g., the skin (e.g.,
psoriasis), cardiovascular system (e.g., atherosclerosis), nervous system (e.g.,
Alzheimer's disease), liver (e.g., hepatitis), kidney (e.g., nephritis), pancreas (e.g.,
pancreatitis), and gastrointestinal organs, e.g., colitis, Crohn's disease and IBD;
acute inflammatory conditions, e.g., endotoxemia, septicemia, toxic shock syndrome

and infectious disease; multiple organ failure; respiratory disease (ARD);
amyloidosis; nephropathies such as glomerulosclerosis, membranous neuropathy,
renal arteriosclerosis, glomerulonephritis, fibroproliferative diseases of the kidney, as
well as other kidney disfunctions and renal tumors. Because of IL-22 and IL-17A
and IL-17F's effects on epithelia, the compositions and combinations of antagonists
described herein can be used to treat epithelial cancers, e.g., carcinoma, melanoma
and others.
[0055] The cytokines IL-22, IL-17A, IL-17F, and IL-23 are known to be
associated with many of these immune disorders and hyperproliferative disorders.
Because the expression and activity of these cytokines are now known to be
associated with a particular type of CD4 effector T cell and to be inter-dependent
upon each other, this invention provides, among other things, methods of treating
diseases by administering compositions comprising agents that antagonize the
activity of IL-22 and at least one of IL-17A, IL-17F, or IL-23.
[0056] One example of a disorder associated with one or more of these
cytokines is psoriasis. A study measuring levels of IL-22 and IL-22R1 RNA in paired
tissue samples (lesion vs. non-lesion) from human psoriatic patients using
quantitative PCR demonstrated that levels of IL-22 and IL-22R1 were upregulated in
psoriatic lesions. Other evidence implicates IL-22 in the development of psoriasis.
For example, transgenic mice that constitutively express IL-22 present with thick
skin, mononuclear immune cell infiltrates, characteristic of psoriatic lesions, and die
soon after birth. WO 03/083062. Similarly, administering IL-22 to mice induces
thickening of skin and mononuclear immune cell infiltrates. WO 03/083062. IL-22
also induces human keratinocyte hyperplasia, suggesting an important role in skin
inflammatory processes. Boniface et al., J. Immunol., (2005) 174:3695-3702. This
application also shows, using quantitative PCR in paired tissue samples (lesion vs.
non-lesion) from human psoriatic patients, that levels of IL-17A, IL-17F, and IL-
23p19 are upregulated in psoriatic lesions. In view of the association of not only IL-
22, but also IL-17A and IL-17F, with psoriasis, this application provides methods of
treating psoriasis by administering compositions comprising agents that antagonize
the activity of IL-22 and at least one of IL-17A, IL-17F, or IL-23p19. Further,
because IL-23 is also associated with psoriasis and the studies described in this
application demonstrate a key role for IL-23 in maintaining IL-22 expression from
Th17 cells, the invention also contemplates administering compositions comprising
an IL-23 antagonist and an antagonist of IL-22, optionally with an antagonist of IL-
17A or lL-17F.
[0057] Another example of a disorder associated with one or more of IL-22, IL-
17A, IL-17F, and IL-23 is rheumatoid arthritis (RA). RA is characterized by
inflammation in the joints. It is the most frequent form of arthritis, involving
inflammation of connective tissue and the synovial membrane, a membrane of the
joint. The inflamed synovial membrane often infiltrates the joint and damages joint
cartilage and bone. Inhibitors of IL-22 ameliorate symptoms in an animal model of
RA (WO 02/068476 A2; U.S. Patent No. 6,939,545). RA is also associated with IL-
23. Recent studies have shown that IL-23p19 deficient mice are resistant to EAE (a
model of multiple sclerosis) and collagen-induced arthritis (CIA - a model of RA),
demonstrating that IL-23 is an important factor in the pathogenesis of these
autoimmune diseases. Mechanistically, this has been attributed to diminished IL-
17A and IL-17F expression in IL-23 deficient mice. However, IL-17A deficient mice,
while developing less severe disease, are still susceptible to CIA, suggesting that IL-
17A does not account for all the functions of IL-23. The studies described in this
application demonstrate a key role for IL-23 in maintaining IL-22 expression from
Th17 cells. Our data indicate that IL-22, like IL-17A and IL-17F, is downstream of IL-
23 signaling in CIA. We have also observed co-expression of IL-22 with IL-17A in
CD4 T cells in mice with CIA. Furthermore, in rheumatoid arthritis patients, IL-22 is
expressed in synovial tissues and mononuclear cells. Treatment of synovial
fibroblasts isolated from patients with IL-22 induced chemokine production (Ikeuchi
H. et al. Arthritis Rheum 52:1037-1046). IL-22 also induced IL-6, IL-8, and a variety
of chemokines and metallomatrix proteinases from colonic myofibroblasts (Andoh, A.
et al. Gastroenterology 129:969-984.). Systemic administration of IL-22 enhanced
circulating amounts of serum amelyoid A (SAA), demonstrating that IL-22 can induce
parameters indicative of an acute phase response (Dumoutier, L. et al 2000. Proc
Natl Acad Sci U SA 97:10144-10149.). IL-23p19 transgenic mice also display
higher concentrations of circulating SAA (Wiekowski, M. et al. 2001 J Immunol.
166:12(7563-70), and our data indicate that this effect is at least partially mediated
by IL-22.
[0058] Accordingly, this application specifically contemplates treating RA
using compositions to inhibit not only IL-22, but also one or both of IL-17A and IL-
17F. The invention further contemplates administering compositions comprising an
antagonist of IL-23 and an antagonist of IL-22, optionally with an antagonist of IL-
17A or IL-17F, since IL-23 influences the production of IL-22 and IL-17 from Th17
cells. In addition to treating RA, the methods of this invention may be used to treat
other arthritic diseases in humans.
[0059] IL-22 is also known to enhance the innate immunity of peripheral
tissues by inducing the expression of anti-microbial peptides including beta-defensin
2 (hBD-2), S100A7, S100A8, and S100A9 (Wolk et al., Immunity (2004) 21:241-54;
Boniface et al., J. Immunol. (2005) 174:3695-3702). Data in this application indicate
that IL-22 and at least one of IL-17A, IL-17F, or IL-23 may be particularly effective in
combating microbial infections by inducing expression of one or more anti-microbial
peptides, and thus enhancing the innate immune response, because IL-22 can act in
cooperation, either additively or synergistically, with IL-17A and IL-17F, and it is
induced by IL-23. Accordingly, this application provides methods of inducing an anti-
microbial peptide in a mammal in need thereof, comprising administering to the
mammal IL-22 and IL-17A, IL-22 and IL-17F, or IL-22, IL-17A, and IL-17F in amounts
effective to induce an anti-microbial peptide. In other embodiments, the method of
inducing an anti-microbial peptide, in a mammal in need thereof, comprises
administering to the mammal IL-22 and IL-23, optionally with IL-17A and/or IL-17F, in
amounts effective to induce an anti-microbial peptide. In still other embodiments, the
anti-microbial peptide is induced in a cell, such as a keratinocyte.
[0060] An acute phase response is a collection of biochemical, physiologic,
and behavioral changes indicative of an inflammatory condition. The modulation of
specific proteins known as acute phase reactants is a biochemical hallmark of an
acute phase response and of inflammation. (Reviewed in Gabay & Kushner, N.
Engl. J. Med. (1999) 340:448-55.) The concentration of some acute-phase proteins
typically increase in response to inflammation. Examples of those proteins include
C-reactive protein, serum amyloid A, fibrinogen, and haptoglobin. The concentration
of other proteins, such as albumin, transferrin, and a-fetoprotein, typically decrease
in the acute phase response. The pattern of expression of acute phase proteins can
vary depending upon the underlying condition, and the pattern of expression and the
relative levels of the various acute phase proteins can be used to deterime the
nature and severity of the inflammation. Data in this application indicate that IL-22
can effect an acute phase response. Accordingly, this application provides methods
of inducing or enhancing the acute phase response by administering IL-22 and at
least one of IL-17A, IL-17F, or IL-23. In another embodiment the application
provides methods of increasing the expression of an acute phase protein, such as C-
reactive protein, serum amyloid A, fibrinogen, or haptoglobin, or decreasing the
expression of an acute phase protein, such as albumin, transferrin, or a-fetoprotein,
by administering IL-22 and at least one of IL-17A, IL-17F, or IL-23. The application
further contemplates administering compositions comprising an antagonist of IL-22,
optionally with an antagonist of one or more of IL-17A, IL-17F, or IL-23 to reduce or
inhibit the acute phase response. In another embodiment the application provides
methods of increasing the expression of an acute phase protein, such as C-reactive
protein, serum amyloid A, fibrinogen, or haptoglobin, or decreasing the expression of
an acute phase protein, such as albumin, transferrin, or a-fetoprotein, by
administering an antagonist of IL-22, optionally with an antagonist of one or more of
IL-17A, IL-17F, or IL-23.
IV. Combination Therapy Comprising Additional Therapeutic Agents
[0061] Although the application includes compositions comprising
combinations of agents that inhibit the activity of IL-22 and at least one of IL-17A, IL-
17F, or IL-23, these compositions may further comprise one or more additional
therapeutic agents that are advantageous for treating various diseases. The term "in
combination" in this context means that the composition comprising the therapeutic
agents is given substantially contemporaneously, either simultaneously or
sequentially, with the composition comprising a combination of agents that inhibit the
activity of one or more of IL-22, IL-17A, IL-17F, or IL-23. In one embodiment, if given
sequentially, at the onset of administration of the second composition, the first of the
two compositions is still detectable at effective concentrations at the site of
treatment. In another embodiment, if given sequentially, at the onset of
administration of the second composition, the first of the two compositions is not
detectable at effective concentrations at the site of treatment.
[0062] For example, the combination therapy can include a composition
comprising at least one anti-IL-22 antibody and at least one anti-IL-17A, anti-IL-17F,
or anti-IL-23 antibody co-formulated with, and/or co-administered with, at least one
additional therapeutic agent. The additional therapeutic agent may include at least
one inhibitor of a cytokine other than IL-22, IL-17A, IL-17F, or IL-23; a growth factor
inhibitor; an immunosuppressant an anti-inflammatory agent; a metabolic inhibitor;
an enzyme inhibitor; a cytotoxic agent; and a cytostatic agent, as described in more
detail below. The compositions and combinations of the invention can be used to
regulate inflammatory conditions associated with IL-22 and at least one of IL-17A, IL-
17F, or IL-23, e.g., by modulating cytokine signaling through receptors located on
fibrobalsts and/or epithelial cells of a variety of tissues, including, but not limited to,
those of the pancreas, skin, lung, gut, liver, kidney, salivary gland, and vascular
endothelia, in addition to potentially activated and tissue localized immune cells.
[0063] In one embodiment, the additional therapeutic agent is a standard
treatment for arthritis, including, but not limited to, non-steroidal anti-inflammatory
agents (NSAIDs); corticosteroids, including prednisolone, prednisone, cortisone, and
triamcinolone; and disease modifying anti-rheumatic drugs (DMARDs), such as
methotrexate, hydroxychloroquine (Plaquenil™) and sulfasalazine, leflunomide
(Arava™), tumor necrosis factor inhibitors, including etanercept (Enbrel™), infliximab
(Remicade™) (with or without methotrexate), and adalimumab (Humira™), anti-
CD20 antibody (e.g., Rituxan™), soluble interleukin-1 receptor, such as anakinra
(Kineret™), gold, minocycline (Minocin™), penicillamine, and cytotoxic agents,
including azathioprine, cyclophosphamide, and cyclosporine. Such combination
therapies may advantageously utilize lower dosages of the administered therapeutic
agents, thus avoiding possible toxicities or complications associated with the various
monotherapies. Moreover, the therapeutic agents disclosed are expected to provide
enhanced and/or synergistic effects.
[0064] The additional therapeutic agents may be those agents that interfere at
different stages in the autoimmune and subsequent inflammatory response. In one
embodiment, the composition comprising a combination of agents that inhibit the
activity of one or more of IL-22, IL-17A, IL-17F, or IL-23 may be co-formulated with,
and/or co-administered with, at least one growth factor antagonist or an antagonist of
a cytokine other than IL-22, IL-17A, IL-17, or IL-23. The antagonists may include
soluble receptors, peptide inhibitors, small molecules, ligand fusions, antibodies (that
bind cytokines or growth factors or their receptors or other cell surface molecules)
and binding fragments thereof, and "anti-inflammatory cytokines" and agonists
thereof.
[0065] Non-limiting examples of the additional therapeutic agents include, but
are not limited to, antagonists of at least one interleukin (e.g., IL-1, lL-2, IL-6, IL-7, IL-
8, IL-12 (or one of its subunits p35 or p40), IL-13, IL-15, IL-16, IL-18, IL-19, IL-20, IL-
21, IL-24, IL-26, IL-28, IL-29, IL-31, and 1L-33); cytokine (e.g., TNFa, LT, EMAP-II,
and GM-CSF); and growth factor (e.g., FGF and PDGF). The agents may also
include, but are not limited to, antagonists of at least one receptor for an interleukin,
cytokine, and growth factor. Inhibitors (e.g., antibodies) of cell surface molecules
such as CD2, CD3, CD4, CD8, CD20 (e.g. Rituxan™), CD25, CD28, CD30, CD40,
CD45, CD69, CD80 (B7.1), CD86 (B7.2), CD90, or their ligands (e.g., CD154 (gp39,
CD40L)), or LFA-1/ICAM-1 and VLA-4/VCAM-1 (Yusuf-Makagiansar et al., Med.
Res. Rev., (2002) 22(2): 146-67)) can also be employed as additional therapeutic
agents. In certain embodiments, antagonists that can be used as additional
therapeutic agents may include antagonists of IL-1, IL-12 (or one of its subunits p35
or p40), TNFa, IL-15, IL-18, IL-19, IL-20, and IL-21, and their receptors.
[0066] Examples of those agents include IL-12 antagonists (such as
antibodies that bind IL-12 (see e.g., WO 00/56772) or one of its subunits p35 or
p40); IL-12 receptor inhibitors (such as antibodies to the IL-12 receptor); and soluble
IL-12 receptor and fragments thereof. Examples of IL-15 antagonists include
antibodies against IL-15 or its receptor, soluble fragments of the IL-15 receptor, and
IL-15-binding proteins. Examples of IL-18 antagonists include antibodies to IL-18,
soluble fragments of the IL-18 receptor, and IL-18 binding proteins (IL-18BP, Mallet
et al., Circ. Res., (2001) 28). Examples of IL-1 antagonists include lnterleukin-1-
Converting Enzyme (ICE) inhibitors (such as Vx740), IL-1 antagonists (e.g., IL-1RA
(ANIKINRA (or Kineret™), AMGEN)), slL-1RII (Immunex), and anti-IL-1 receptor
antibodies.
[0067] Examples of TNF antagonists include antibodies to TNF (e.g., human
TNFa), such as D2E7 (human anti-TNFa antibody, U.S. 6,258,562, Humira™,
BASF); CDP-571/CDP-870/BAY-10-3356 (humanized anti-TNFa antibodies,
Celltech/Pharmacia); cA2 (chimeric anti-TNFa antibody, Remicade™, Centocor);
and anti-TNF antibody fragments (e.g., CPD870). Other examples include soluble
TNF receptor (e.g., human p55 or p75) fragments and derivatives thereof, such as
p55 kdTNFR-IgG (55 kD TNF receptor-IgG fusion protein, Lenercept™) and 75
kdTNFR-IgG (75 kD TNF receptor-IgG fusion protein, Enbrel™, Immunex, see, e.g.,
Arthritis & Rheumatism, (1994) Vol. 37, S295; J. Invest. Med., (1996) Vol. 44, 235A).
Further examples include enzyme antagonists (e.g., TNFa converting enzyme
inhibitors (TACE) such as alpha-sulfonyl hydroxamic acid derivative (WO 01/55112)
or N-hydroxyformamide inhibitor (GW 3333, -005, or -022)) and TNF-bp/s-TNFR
(soluble TNF binding protein, see e.g., Arthritis & Rheumatism (1996) Vol. 39, No. 9
(supplement), S284; and Am. J. Physiol. Heart Circ. Physiol. (1995) Vol. 268, pp.
37-42). TNF antagonists may be soluble TNF receptor (e.g., human p55 or p75)
fragments and derivatives, such as 75 kdTNFR-IgG; and TNFa converting enzyme
(TACE) inhibitors.
[0068] In other embodiments, the composition comprising a combination of
agents that inhibit the activity of one or more of IL-22, IL-17A, IL-17F, or IL-23 can be
administered in combination with at least one of the following: IL-13 antagonists,
such as soluble IL-13 receptors and/or anti-IL-13 antibodies; and IL-2 antagonists,
such as IL-2 fusion proteins (e.g., DAB 486-IL-2 and/or DAB 389-IL-2, Seragen, see
e.g., Arthritis & Rheumatism, (1993) Vol. 36,1223) and anti-IL-2R antibodies (e.g.,
anti-Tac (humanized antibody, Protein Design Labs, see Cancer Res., (1990)
50(5):1495-502)). Another additional therapeutic agent that can be combined with a
composition comprising a combination of agents that inhibit the activity of one or
more of IL-22, IL-17A, IL-17F, or IL-23 is non-depleting anti-CD4 inhibitors such as
IDEC-CE9.1/SB 210396 (anti-CD4 antibody, IDEC/SmithKline). Yet other additional
therapeutic agents that can be combined with a composition comprising a
combination of agents that inhibit the activity of one ore more of IL-22, IL-17A, IL-
17F, or IL-23 include antagonists (such as antibodies, soluble receptors, or
antagonistic ligands) of costimulatory molecules, such as CD80 (B7.1) and CD86
(B7.2); ICOSL, ICOS, CD28, and CTLA4 (e.g., CTLA4-lg (atabacept)); P-selectin
glycoprotein ligand (PSGL); and anti-inflammatory cytokines and agonists thereof
(e.g., antibodies). The anti-inflammatory cytokines may include IL-4
(DNAX/Schering); IL-10 (SCH 52000, recombinant IL-10, DNAX/Schering); IL-13;
and TGF.
[0069] In other embodiments, the additional therapeutic agent that can be
combined with a composition comprising a combination of agents that inhibit the
activity of one ore more of IL-22, IL-17A, IL-17F, or IL-23 is at least one anti-
inflammatory drug, immunosuppressant, metabolic inhibitor, and enzymatic inhibitor.
Non-limiting examples of such drugs or inhibitors include, but are not limited to, at
least one of: non-steroidal anti-inflammatory drug (NSAID) (such as ibuprofen,
Tenidap (see e.g., Arthritis & Rheumatism, (1996) Vol. 39, No. 9 (supplement),
S280)), Naproxen (see e.g., Neuro Report, (1996) Vol. 7, pp. 1209-1213),
Meloxicam, Piroxicam, Diclofenac, and Indomethacin); Sulfasalazine (see e.g.,
Arthritis & Rheumatism (1996) Vol. 39, No. 9 (supplement), S281); corticosteroid
(such as prednisolone); cytokine suppressive anti-inflammatory drug (CSAID); and
an inhibitor of nucleotide biosynthesis (such as an inhibitor of purine biosynthesis
(e.g., folate antagonist such as methotrexate)) or an inhibitor of pyrimidine
biosynthesis (e.g., a dihydroorotate dehydrogenase (DHODH), such as leflunomide
(see e.g., Arthritis & Rheumatism, (1996) Vol. 39, No. 9 (supplement), S131;
Inflammation Research, (1996) Vol. 45, pp. 103-107)).
[0070] Examples of additional inhibitors include at least one of: corticosteroid
(oral, inhaled and local injection); immunosuppressant (such as cyclosporin and
tacrolimus (FK-506)); a mTOR inhibitor (such as sirolimus (rapamycin) or a
rapamycin derivative (e.g., ester rapamycin derivative such as CCI-779 (Elit. L,
Current Opinion Investig. Drugs, (2002) 3(8): 1249-53; Huang, S. et al., Current
Opinion Investig. Drugs (2002) 3(2):295-304))); an agent which interferes with the
signaling of proinflammatory cytokines such as TNFa and IL-1 (e.g., IRAK, NIK, IKK,
p38 or a MAP kinase inhibitor); a COX2 inhibitor (e.g., celecoxib and variants thereof
(MK-966), see e.g., Arthritis & Rheumatism, (1996) Vol. 39, No. 9 (supplement),
S81); a phosphodiesterase inhibitor (such as R973401, see e.g., Arthritis &
Rheumatism, (1996) Vol. 39, No. 9 (supplement), S282)); a phospholipase inhibitor
(e.g., an inhibitor of cytosolic phospholipase 2 (cPLA2) such as trifluoromethyl
ketone analogs (U.S. 6,350,892)); an inhibitor of vascular endothelial cell growth
factor (VEGF); an inhibitor of the VEGF receptor; and an inhibitor of angiogenesis.
[0071] The composition comprising a combination of agents that inhibit the
activity of IL-22 and at least one of IL-17A, IL-17F, or IL-23 disclosed herein can be
used in combination with additional therapeutic agents to treat specific immune
disorders as discussed in further detail below.
[0072] Non-limiting examples of additional therapeutic agents for treating
arthritic disorders (e.g., rheumatoid arthritis, inflammatory arthritis, rheumatoid
arthritis, juvenile rheumatoid arthritis, osteoarthritis and psoriatic arthritis) include at
least one of the following: TNF antagonists (such as anti-TNF antibodies); soluble
fragments of TNF receptors (e.g., human p55 and p75) and derivatives thereof (such
as p55 kdTNFR-IgG (55 kD TNF receptor-IgG fusion protein, Lenercept™) and 75
kdTNFR-IgG (75 kD TNF receptor-IgG fusion protein, Enbrel™)); TNF enzyme
antagonists (such as TACE inhibitors); antagonists of IL-12 (or one of its subunits
p35 or p40), IL-15, IL-18, IL-19, IL-20, IL-21, and IL-24; T cell and B cell depleting
agents (such as anti-CD4, anti-CD20, or anti-CD22 antibodies); small molecule
inhibitors (such as methotrexate and leflunomide); sirolimus (rapamycin) and
analogs thereof (e.g., CCI-779); Cox-2 and cPLA2 inhibitors; NSAIDs; p38, TPL-2,
Mk-2, and NFkB inhibitors; RAGE or soluble RAGE; P-selectin or PSGL-1 inhibitors
(such as small molecule inhibitors and antibodies to); estrogen receptor beta (ERB)
agonists, and ERB-NFkB antagonists.
[0073] Non-limiting examples of additional therapeutic agents for treating
multiple sclerosis include interferon-ß for example, IFNß-1a and IFNß-1b), Copaxone,
corticosteroids, IL-1 inhibitors, TNF inhibitors, antibodies to CD40 ligand, antibodies
to CD80, and IL-12 antagonists.
[0074] Non-limiting examples of additional therapeutic agents for treating
inflammatory bowel disease or Crohn's disease include budenoside; epidermal
growth factor; corticosteroids; cyclosporine; sulfasalazine; aminosalicylates; 6-
mercaptopurine; azathioprine; metronidazole; lipoxygenase inhibitors; mesalamine;
olsalazine; balsalazide; antioxidants; thromboxane inhibitors; IL-1 receptor
antagonists; anti-IL-1 monoclonal antibodies; anti-IL-6 monoclonal antibodies; growth
factors; elastase inhibitors; pyridinyl-imidazole compounds; TNF antagonists as
described herein; IL-4, IL-10, IL-13, and/or TGFß or agonists thereof (e.g., agonist
antibodies); IL-11; glucuronide- or dextran-conjugated prodrugs of prednisolone,
dexamethasone or budesonide; ICAM-1 antisense phosphorothioate
oligodeoxynucleotides (ISIS 2302; Isis Pharmaceuticals, Inc.); soluble complement
receptor 1 (TP10; T Cell Sciences, Inc.); slow-release mesalazine; methotrexate;
antagonists of Platelet Activating Factor (PAF); ciprofloxacin; and lignocaine.
[0075] Non-limiting examples of additional therapeutic agents for regulating
immunue responses, e.g., treating or inhibiting transplant rejection and graft-versus-
host disease, include the following: antibodies against cell surface molecules,
including but not limited to CD25 (IL-2 receptor a), CD11a (LFA-1), CD54 (ICAM-1),
CD4, CD45, CD28/CTLA4, CD80 (B7-1), CD86 (B7-2), or combinations thereof, and
general immunosuppressive agents, such as cyclosporin A or FK506.
[0076] Another aspect of the present invention accordingly relates to kits for
carrying out the administration of a composition comprising a combination of agents
that inhibit the activity of IL-22 and at least one of IL-17A, IL-17F, or IL-23, optionally
with additional therapeutic agents. In one embodiment, the kit comprises a
composition comprising an IL-22 antagonist, and an antagonist of at least one of IL-
17A, IL-17F, or IL-23 formulated in a pharmaceutical carrier. The kit may further
comprise at least one additional therapeutic agent, formulated as appropriate in one
or more separate pharmaceutical preparations.
V. Pharmaceutical Compositions and Methods of Administration
[0077] Certain methods described in this application utilize compositions
suitable for pharmaceutical use and administration to patients. These compositions
comprise a pharmaceutical excipient and one or more antibodies, one or more
soluble receptors, one or more binding proteins, or combinations of those antibodies,
soluble receptors, and/or binding proteins. As used herein, "pharmaceutical
excipient" includes solvents, dispersion media, coatings, antibacterial and antifungal
agents, isotonic and absorption delaying agents, etc., that are compatible with
pharmaceutical administration. Use of these agents for pharmaceutically active
substances is well known in the art. The compositions may also contain other active
compounds providing supplemental, additional, or enhanced therapeutic functions.
The pharmaceutical compositions may also be included in a container, pack, or
dispenser together with instructions for administration.
[0078] A pharmaceutical composition can be formulated to be compatible with
its intended route of administration. Methods to accomplish the administration are
known to those of ordinary skill in the art. It may also be possible to create
compositions which may be topically or orally administered, or which may be capable
of transmission across mucous membranes. For example, the administration may
be intravenous, intraperitoneal, intramuscular, intracavity, subcutaneous, cutaneous,
or transdermal.
[0079] Solutions or suspensions used for intradermal or subcutaneous
application typically include at least one of the following components: a sterile diluent
such as water, saline solution, fixed oils, polyethylene glycol, glycerine, propylene
glycol, or other synthetic solvent; antibacterial agents such as benzyl alcohol or
methyl parabens; antioxidants such as ascorbic acid or sodium bisulfite; chelating
agents such as ethylenediaminetetraacetic acid (EDTA); buffers such as acetate,
citrate, or phosphate; and tonicity agents such as sodium chloride or dextrose. The
pH can be adjusted with acids or bases. Such preparations may be enclosed in
ampoules, disposable syringes, or multiple dose vials.
[0080] Solutions or suspensions used for intravenous administration include a
carrier such as physiological saline, bacteriostatic water, Cremophor EL™ (BASF,
Parsippany, NJ), ethanol, or polyol. In all cases, the composition must be sterile and
fluid for easy syringability. Proper fluidity can often be obtained using lecithin or
surfactants. The composition must also be stable under the conditions of
manufacture and storage. Prevention of microorganisms can be achieved with
antibacterial and antifungal agents, e.g., parabens, chlorobutanol, phenol, ascorbic
acid, thimerosal, etc. In many cases, isotonic agents (sugar), polyalcohols (mannitol
and sorbitol), or sodium chloride may be included in the composition. Prolonged
absorption of the composition can be accomplished by adding an agent which delays
absorption, e.g., aluminum monostearate and gelatin.
[0081] Oral compositions include an inert diluent or edible carrier. The
composition can be enclosed in gelatin or compressed into tablets. For the purpose
of oral administration, the antibodies can be incorporated with excipients and placed
in tablets, troches, or capsules. Pharmaceutically compatible binding agents or
adjuvant materials can be included in the composition. The tablets, troches, and
capsules, may contain (1) a binder such as microcrystalline cellulose, gum
tragacanth or gelatin; (2) an excipient such as starch or lactose, (3) a disintegrating
agent such as alginic acid, Primogel, or corn starch; (4) a lubricant such as
magnesium stearate; (5) a glidant such as colloidal silicon dioxide; or (6) a
sweetening agent or a flavoring agent.
[0082] The pharmaceutical composition may also be administered by a
transmucosal or transdermal route. For example, antibodies that comprise a Fc
portion may be capable of crossing mucous membranes in the intestine, mouth, or
lungs (via Fc receptors). Transmucosal administration can be accomplished through
the use of lozenges, nasal sprays, inhalers, or suppositories. Transdermal
administration can also be accomplished through the use of a composition
containing ointments, salves, gels, or creams known in the art. For transmucosal or
transdermal administration, penetrants appropriate to the barrier to be permeated
are used. For administration by inhalation, the antibodies are delivered in an aerosol
spray from a pressured container or dispenser, which contains a propellant (e.g.,
liquid or gas) or a nebulizer.
[0083] In certain embodiments, the pharmaceutical compositions are prepared
with carriers to protect the active component against rapid elimination from the body.
Biodegradable polymers (e.g., ethylene vinyl acetate, polyanhydrides, polyglycolic
acid, collagen, polyorthoesters, polylactic acid) are often used. Methods for the
preparation of such formulations are known by those skilled in the art. Liposomal
suspensions can be used as pharmaceutically acceptable carriers too. The
liposomes can be prepared according to established methods known in the art (U.S.
Patent No. 4,522,811).
[0084] The pharmaceutical compositions are administered in therapeutically
effective amounts as described. Therapeutically effective amounts may vary with the
subject's age, condition, sex, and severity of medical condition. Appropriate dosage
may be determined by a physician based on clinical indications. The compositions
may be given as a bolus dose to maximize the circulating levels of active component
of the composition for the greatest length of time. Continuous infusion may also be
used after the bolus dose.
[0085] As used herein, the term "subject" is intended to include human and
non-human animals. The term "non-human animals" of the invention includes all
vertebrates, such as non-human primates, sheep, dogs, cows, chickens,
amphibians, reptiles, etc.
[0086] Examples of dosage ranges that can be administered to a subject can
be chosen from: 1 µg/kg to 20 mg/kg, 1 µg/kg to 10 mg/kg, 1 µg/kg to 1 mg/kg, 10
µg/kg to 1 mg/kg, 10 µg/kg to 100 Mg/kg, 100 µg/kg to 1 mg/kg, 250 µg/kg to 2
mg/kg, 250 µg/kg to 1 mg/kg, 500 µg/kg to 2 mg/kg, 500 pg/kg to 1 mg/kg, 1 mg/kg
to 2 mg/kg, 1 mg/kg to 5 mg/kg, 5 mg/kg to 10 mg/kg, 10 mg/kg to 20 mg/kg, 15
mg/kg to 20 mg/kg, 10 mg/kg to 25 mg/kg, 15 mg/kg to 25 mg/kg, 20 mg/kg to 25
mg/kg, and 20 mg/kg to 30 mg/kg (or higher). These dosages may be administered
daily, weekly, biweekly, monthly, or less frequently, for example, biannually,
depending on dosage, method of administration, disorder or symptom(s) to be
treated, and individual subject characteristics. Dosages can also be administered
via continuous infusion (such as through a pump). The administered dose may also
depend on the route of administration. For example, subcutaneous administration
may require a higher dosage than intravenous administration.
[0087] In certain circumstancs, it may be advantageous to formulate
compositions in dosage unit form for ease of administration and uniformity of
dosage. Dosage unit form as used herein refers to physically discrete units suited
for the patient. Each dosage unit contains a predetermined quantity of antibody
calculated to produce a therapeutic effect in association with the carrier. The dosage
unit depends on the characteristics of the antibodies and the particular therapeutic
effect to be achieved.
[0088] Toxicity and therapeutic efficacy of the pharmaceutical composition
can be determined by standard pharmaceutical procedures in cell cultures or
experimental animals, e.g., determining the LD50 (the dose lethal to 50% of the
population) and the ED50 (the dose therapeutically effective in 50% of the
population). The dose ratio between toxic and therapeutic effects is the therapeutic
index and it can be expressed as the ratio LD50/ED50.
[0089] The data obtained from the cell culture assays and animal studies can
be used to formulate a dosage range in humans. The dosage of these compounds
may lie within the range of circulating antibody concentrations in the blood, which
includes an ED50 with little or no toxicity. The dosage may vary within this range
depending upon the dosage composition form employed and the route of
administration. The therapeutically effective dose can be estimated initially using cell
culture assays. A dose may be formulated in animal models to achieve a circulating
plasma concentration range that includes the IC50 (i.e., the concentration of agent
which achieves a half-maximal inhibition of symptoms). The effects of any particular
dosage can be monitored by a suitable bioassay. Examples of suitable bioassays
include DNA replication assays, transcription-based assays, receptor-binding
assays, and other immunological assays.
VI. Diagnostic Uses
[0090] The antagonists may also be used to detect the presence of IL-22, and
at least one of IL-17A, IL-17F, or IL-23 in a biological sample. These cytokines can
be detected either extracellularly or intracellularly using methods known in the art,
including the methods disclosed in this application. By correlating the presence or
level of these proteins with a medical condition, one of skill in the art can diagnose
the associated medical condition. For example, IL-22 induces changes associated
with those caused by inflammatory cytokines (such as IL-1 and TNFa), and inhibitors
of IL-22 ameliorate symptoms in an animal model of rheumatoid arthritis (WO
02/068476 A2). As disclosed in this application, IL-22 is co-expressed with IL-17A
and IL-17F in psoriatic lesions and functions in synergy with those cytokines to
enhance the expression of anti-microbial peptides. Therefore, illustrative medical
conditions that may be diagnosed in accordance with this disclosure include
psoriasis and rheumatoid arthritis. Multiple sclerosis, inflammatory bowel disease,
and Crohn's disease can also be diagnosed in accordance with this application.
Further, since this application shows that IL-22 can induce an acute-phase response,
that response can be monitored using methods in accordance with the disclosure.
[0091] Antibody-based detection methods are well known in the art, and
include ELISA, radioimmunoassays, immunoblots, Western blots, flow cytometry,
immunofluorescence, immunoprecipitation, and other related techniques. The
antibodies may be provided in a diagnostic kit. The kit may contain other
components, packaging, instructions, or other material to aid the detection of the
protein and use of the kit.
[0092] Antibodies may be modified with detectable markers, including ligand
groups (e.g., biotin), fluorophores and chromophores, radioisotopes, electron-dense
reagents, or enzymes. Enzymes are detected by their activity. For example,
horseradish peroxidase is detected by its ability to convert tetramethylbenzidine
(TMB) to a blue pigment, quantifiable with a spectrophotometer. Other suitable
binding partners include biotin and avidin, IgG and protein A, and other
receptor-ligand pairs known in the art.
[0093] Antibodies can also be functionally linked (e.g., by chemical coupling,
genetic fusion, non-covalent association or otherwise) to at least one other molecular
entity, such as another antibody (e.g., a bispecific or a multispecific antibody), toxins,
radioisotopes, cytotoxic or cytostatic agents, among others. Other permutations and
possibilities are apparent to those of ordinary skill in the art, and they are considered
equivalents within the scope of this invention.
[0094] When the detection method is an in vitro method, it includes: (1)
contacting the sample or a control sample with a first reagent that binds to IL-22 and
a second reagent that binds to IL-17A, IL-17F, or IL-23, and (2) detecting formation
of a complex between the first and second reagents and the sample or the control
sample, wherein a statistically significant change in the formation of the complex in
the sample relative to a control sample, is indicative of the presence of the cytokines
in the sample. In one embodiment, the method includes contacting a sample
comprising cells with a labeled regeant, such as a fluorescent antibody, that binds to
IL-22, IL-17A, IL-17F, or IL-23 within the cells. The amount of reagent detected
within a cell is directly proportional to the amount of intracellular IL-22, IL-17A, IL-
17F, or IL-23 expressed within the cell.
[0095] The detection method can also be an in vivo detection method (e.g., in
vivo imaging in a subject). The method can be used to diagnose a disorder, e.g., a
disorder as described herein. The method includes: (1) administering a first reagent
that binds to IL-22 and a second reagent that binds to IL-17A, IL-17F, or IL-23 to a
subject or a control subject under conditions that allow binding of the first and
second reagents to their cytokines, and (2) detecting formation of a complex
between the first and second reagents and their cytokines, wherein a statistically
significant change in the formation of the complex in the subject relative to a control,
e.g., a control subject, is indicative of the presence of the cytokines.
EXAMPLES
Example 1: IL-22 transcript is more highly expressed in Th17 cells than in Th1
or Th2 cells.
[0096] Th17 cells are thought to produce IL-17A and IL-17F in a lineage
specific manner. In order to identify other potential Th17 cytokines, naive
(CD62LHiCD4+) T cells purified from C.Cg-Tg(D011.10)1 ODIo TCR transgenic mice
(Jackson Laboratories) were differentiated to the Th1 (IL-12, anti-IL-4), Th2 (IL-4,
anti-IFN-?), and Th17 (TGF-p, IL-6, IL-1 (3, TNF-a, IL-23, anti-IFN-?, and anti-IL-4)
lineages. NaTve (CD62LH,CD4+) T cells were purified from spleens of DO11 mice by
CD4 negative selection followed by CD62L positive selection according to the
manufacturer's directions (Miltenyi Biotec). All lymphocyte cultures were grown in
RPMI 1640 supplemented with 10% FBS, 2 mM L-glutamine, 5 mM HEPES, 100
U/ml Pen-Strep, and 2.5 µM ß-mercaptoethanol. Purity of CD4+CD62LHi cells was
above 98%. 2x105 D011 T cells were cultured with 4x106 irradiated BALB/cByJ
splenocytes (3300 rad) and 1 µg/ml OVA323-339 peptide (OVAp) (New England
Peptide). Recombinant cytokines were used at 10 ng/ml, except for IL-4 (1 ng/ml)
and TGF-ß (20 ng/ml). Neutralizing antibodies were used at 10 µg/ml. Murine IL-4,
IL-6, IL-12, IL-23, and TNF-a were purchased from R&D Systems. TGF-ß was
purchased from Sigma. IL-1ß was obtained from Bender Medsystems. Antibodies
to IFN-?(XMG1.2) and IL-4 (BVD4-1D11) were purchased from Pharmingen. After
differentiating for 7 days, CD4 T cells were re-purified and rested overnight. CeHs
were then restimulated with 50 ng/ml PMA, 1 µg/ml ionomycin, and with the following
conditions: Th1 cells (IL-12, anti-IL-4), Th2 cells (IL-4, anti-IFN-?), or Th17 (IL-23,
anti-IFN-?, anti-IL-4) for 6 hrs. The expression of cytokines after restimulation were
then examined by quantitative PCR. RNA was prepared and quantitative PCR for
cytokine transcripts was performed using SYBR Green Platinum Taq (Invitrogen)
and pre-qualified primers (Qiagen). All cytokine concentrations were normalized to
HPRT. Fold induction was calculated using the AACt method relative to purified,
unactivated naive D011 T cells. Data shown in Figure 1 are average ± SD and are
representative of two experiments.
[0097] Th1 cells expressed the highest amounts of IFN-? transcript, Th2 cells
had the highest abundance of IL-4, and Th17 cells produced the greatest abundance
of IL-17A and IL-17F, demonstrating that these cells were successfully differentiated
(Figure 1 A). Of 22 additional interleukins examined, IL-22 transcript was higher in
Th17 cells relative to Th1 cells by -120 fold and relative to Th2 cells by -700 fold
(Figure 1B). In contrast, expression of IL-2, IL-3, IL-5, IL-6, IL-9, IL-10, IL-13, IL-21,
IL-24, IL-25, and IL-31 was equivalent or more abundant in Th1 or Th2 cells
compared to Th17 (Figure 1C). Other cytokines including IL-1, IL-7, IL-11, IL-15, IL-
16, IL-18, IL-19, IL-20, IL-27, and IL-28 were not expressed highly in any of the T cell
lineages (Figure 1D). Therefore, IL-22 transcript was identified as one of 22
interleukin transcripts examined that is expressed at higher amounts by Th17 cells
than by Th1 or Th2.
Example 2: Th17 cells are the main producers of IL-22.
[0098] IL-22 is a member of the IL-10 family, along with IL-10, IL-19, IL-20, IL-
24, and IL-26 (Dumoutier et al., J Immunol, (2000) 164:1814-19; Xie et al., J. Biol.
Chem. (2000) 275:31335-39; Renauld et al., Nat. Rev. Immunol. (2003) 3:667-76;
Pestka et al., Ann. Rev. Immunol. (2004) 22:929-79). Members of this family share
strong structural homology with IL-10. Human IL-22 is located on chromosome
12q15 (mouse chromosome 10), approximately 90 kb away from the IFN-? locus.
Previous reports have demonstrated that activation of human CD4 T cells with IL-12
and anti-IL-4 enhanced IL-22 transcript expression, suggesting that Th1 cells
express IL-22 (Wolk et al., J. Immunol. (2002) 168:5397-402; Gurney, A.L., Int.
Immunopharmacol. (2004) 4:669-677). However, the expression of IL-22 protein
from T cells has not been reported.
[0099] To examine IL-22 protein expression, monoclonal antibodies (Ab-01,
Ab-02, Ab-03) to murine IL-22 were generated using methods similar to those
described previously (Li et al., Int. Immunopharmacol. (2004) 4:693-708) and IL-22
protein concentrations were determined by ELISA. Naive DO11 T cells were
activated with irradiated splenocytes, 1µg/ml OVAp, and various cytokines and
antibodies as indicated. Murine IL-4, IL-6, IL-12, IL-23, and TNF-a, were purchased
from R&D Systems. TGF-ß was purchased from Sigma. Murine IL-1ß was obtained
from Bender Medsystems. IL-22 and IL-17F were generated by methods as
previously described (Li et al., Int. Immunopharmacol. (2004) 4:693-708). Antibodies
to IFN-?(XMG1.2), IL-4 (BVD4-1D11), IL-17A (TC11-18H10), and CD4 (RM4-5)
were purchased from Pharmingen. Anti-D011 antibody (KJ126) was purchased
from Caltag laboratories. IL-22, IL-17A, and IFN-? concentrations were determined
by ELISA on conditioned media from d5 of activation. Antibody pairs (coating,
detection) were used to detect IFN-? (AN-18, R4-6A2, Ebioscience), IL-17A
(MAB721, BAF421, R&D Systems) and IL-22 (Ab-01, biotinylated Ab-03).
[00100] Naive D011 T cells activated with OVA323-339(OVAp) only (ThO)
produced minimal amounts of IL-22 (<100 pg/ml) (Figure 2A). Although IL-22
expression was enhanced during Th1 (110 fold) and Th2 (40 fold) differentiation as
compared to ThO, activation with IL-17 inducing conditions resulted in an even
greater increase in IL-22 production. TGF-ß, IL-6, IL-1ß, and TNF-a enhanced IL-22
expression by 360 fold, whereas activation with IL-23, anti-IFN-?, and anti-IL-4
increased IL-22 production by 460 fold. A combination of these conditions (Th17)
yielded the greatest expression of IL-22, -2400 fold higher than ThO and -22 fold
higher than Th1. These data demonstrate that IL-22 protein is expressed most
abundantly during Th17 differentiation.
[00101] Because some IL-22 was induced under Th1 and Th2 conditions
during primary T cell activation, IL-22 production following a secondary stimulation of
these cells was examined. Naive DO11 cells were differentiated under Th1, Th2, or
Th17 conditions or with TGF- p, IL-6, IL-1ß, and TNF-a. On d7, cells were
harvested, washed extensively, and rested overnight. 2x105 DO11 T cells were
restimulated with 4x106 irradiated splenocytes, 5 ng/ml IL-2 (Sigma), and IL-12 and
anti-IL-4, IL-4 and anti-IFN-?, or IL-23, anti-IFN-?, and anti-IL-4 were added as
indicated. IL-22 concentrations were determined on day 5. Data shown are average
±SD. (Figure 2B)
[00102] Upon restimulation of these cells with OVAp and irradiated
splenocytes, cells originally differentiated with TGF-ß, IL-6, IL-1ß, and TNF-a or with
Th17 conditions produced at least 5 fold more IL-22 than Th1 or Th2 cells. (Figure
2B) The continued differentiation of T cells along the Th17 lineage by restimulating
with IL-23, anti-IFN-?, and anti-IL-4 enhanced IL-22 production by at least 12 fold
over restimulation of cells with OVAp alone or with IL-12 and anti-IL-4. In contrast,
IL-22 production was not enhanced by restimulation of Th1 cells with IL-12, anti-IL-4
or of Th2 cells with IL-4, anti-IFN-?. These results show that further differentiation
towards Th1 or Th2 does not enhance IL-22 production. In addition, restimulation of
Th1 and Th2 cells with IL-23, anti-IFN-?, and anti-IL-4 did not enhance IL-22
production to that observed with Th17 cells activated under the same conditions.
These data demonstrate that IL-23 is more potent than IL-12 in stimulating IL-22
expression and that Th17 cells are the major producers of IL-22.
[00103] IL-22R1 transcript was not detected in any T cell population (Figure
3A). The ability of IL-22 to modulate proliferation or IFN-?, IL-4, and IL-17A
production from naive, Th1, Th2, and Th17 cells was also examined, but no changes
were observed when T cells were treated with exogenous IL-22 (Figures 3B-3E). IL-
17A or IL-17F also did not induce IL-22 expression from naive, Th1, Th2, or Th17
cells. Thus, IL-22 and IL-17A/IL-17F do not directly modulate each other's
expression by CD4 T cells.
[00104] The induction of IL-22 during Th17 differentiation suggests that IL-22
and IL-17 can be co-expressed by the same T cell. To examine this, intracellular
cytokine staining was performed on T cells activated under various conditions.
Intracellular cytokine staining for IFN-?, IL-17A, and IL-22 was performed on cells
from Figure 2A on d5 of activation. Cells were restimulated with 50 ng/ml PMA
(Sigma), 1 µg/ml ionomycin (Sigma), and GolgiPlug (Pharmingen) for 6 hours. Cells
were first stained for surface antigens and then treated with Cytofix/Cytoperm
(Pharmingen) according to manufacturer's directions. Intracellular cytokine staining
was performed using antibodies to IFN-?, IL-22, IL-17A, and IL-17F. Anti-IL-22 (-02)
was labeled with Alexa 647 (Molecular Probes) and anti-IL-17F (15-1) was labeled
with FITC (Pierce Biotechnologies) according to manufacturer's directions. All plots
are gated on KJ126+CD4+ cells and positive percentages shown. ThO, Th1, and Th2
activated cells had minimal expansion of IL-22 producing cells (<0.2%) (Figure 4A).
Activation under Th17 conditions generated a substantial population of IL-22
expressing cells (8.7%), with 81% of IL-22+ cells expressing IL-17A and only 1%
expressing IFN-?.
[00105] The roles of individual cytokines under Th17 differentiation conditions
were further examined. Naive D011 T cells were activated with 1 µg/ml OVAp,
irradiated splenocytes, and the indicated cytokines. Intracellular cytokine staining for
IL-17A, IL-17F, and IL-22 was performed on d5 of activation. Data are
representative of 3 experiments. Only 0.2% of cells activated with exogenous TGF-ß
expressed IL-22 (Figure 4B). Activation with IL-6, IL-1ß, and TNF-a enhanced IL-22+
cells (1.9%). Addition of exogenous TGF-ß to IL-6, IL-1ß, and TNF-a further
increased IL-22+ cells (2.8%), with 62% of IL-22+cells expressing IL-17A or IL-17F.
Activation with IL-23, along with TGF-ß, IL-6, IL-1ß, and TNF-a, led to an ~3 fold
increase in IL-22+ cells (9.5%) (Figure 4B). Eighty percent of IL-22+ cells produced
either IL-17A or IL-17F, with the majority of cells expressing both IL-17A or IL-17F
(44%) (Figure 4B). The addition of a neutralizing antibody to TGF-ß indicated that
exogenous TGF-ß is important for optimal expression of IL-22 induced by IL-6, IL-1ß
and TNF-a (Figure 4C). In summary, these data demonstrate that IL-22 protein is
produced in greater amounts by Th17 cells and that IL-22 is co-expressed with both
IL-17A and IL-17F during Th17 differentiation.
Example 3: IL-23 enhances the expansion of IL-22 producing cells during
Th17 differentiation.
[00106] To further examine how IL-23 enhances IL-22 expression during Th17
differentiation, naive D011 T cells labeled with CFSE (Molecular Probes) were
differentiated with 1 µg/ml OVAp irradiated splenocytes, TGF-ß, and IL-6. TNF-a, IL-
1ß, IL-23 or IL-12 was added to some cultures. The expression of IL-22 was
analyzed from d1 to d5 of culture. Intracellular cytokine staining for IL-22 and IL-17A
was performed on d1 through d5. The percentages of IL-22+ cells on d1-d5 were
determined. Figure 5A shows the percentage of cells expressing IL-22 plotted as a
function of time and representative flow cytometry plots from d2 and d4. Cells
activated with only TGF-ß and IL-6 peaked in IL-22 (15%) expression on d2 and
decreased substantially by d3. Neither TNF-a, IL-1ß, nor IL-12 addition prevented
the decrease in expression of IL-22 observed after d2. In contrast, cells activated
with IL-23, TGF-ß, and IL-6 expressed at least 5 fold more IL-22 on day 4.
[00107] To examine if IL-23 was inducing the expansion of IL-22 producing
cells, we analyzed the CFSE dilution profiles of cells expressing IL-22 and/or IL-17A
on d4 (Figure 5B). No differences in CFSE were observed between IL-22 IL-17A+
and IL-22IL-17A cells activated with TGF-ß and IL-6 alone, or when supplemented
with IL-1 (3, TNF-a, or IL-23. This suggests that there is no correlation between IL-
17A expression and proliferation. CFSE profiles of IL-22+IL-17A- and IL-22+IL-17A+
cells activated with TGF-ß and IL-6 indicated that these cells had proliferated less
than IL-22IL-17A- and IL-22-IL-17A+ cells. Similar findings were observed in cultures
supplemented with IL-1ß, TNF-a or IL-12. In contrast, IL-23 in the context of TGF-ß
and IL-6 enhanced the proliferation and expansion of IL-22+IL-17A and IL-22+IL-
17A+ cells. These findings demonstrate that IL-23 drives the expansion of IL-22
producing cells in the Th17 lineage.
[00108] To examine if endogenous IL-23 is necessary for optimal IL-22
expression, naive DO11 T cells were activated with LPS treated dendritic cells
("DCs"), OVAp, and neutralizing antibodies to IL-23R or to IL-12p40. To generate
DCs, bone marrow cells were cultured with 10 ng/ml GM-CSF and 1 ng/ml IL-4 for 7
days. After purification by CD11c positive selection (Miltenyi Biotec), DCs were
matured for 24 hours with 1 µg/ml LPS (E. Coli Serotype 0111-B4, Sigma). DCs
were then washed, and 1x104 DCs were cultured with 2x104 purified naive DO11 T
cells, OVAp, and 10 µg/ml anti-IL-12p40, anti-IL-23R, or relevant isotype controls.
[00109] Anti-IL-12p40 (C17.8) and anti-IL-23R (258010) were obtained from
R&D Systems. IL-22 concentrations were determined on d5 of culture. Data are
representative of at least 2 experiments. Neutralization of IL-23R reduced IL-22
production by 62% (at 1 µg/mL OVAp) as compared to isotype control (Figure 5C).
A similar reduction of IL-22 expression was observed with anti-IL-12p40 (64%),
suggesting that IL-23, and not IL-12, is responsible for the majority of IL-22
production. Taken together, these data demonstrate that IL-23 induces optimal
expansion of IL-22 producing cells.
Example 4: Expression of mouse IL-22 requires IL-6 and IL-23.
[00110] IL-23 can induce expression of IL-22 from mouse T cells in vitro. To
examine how IL-23 affects IL-22 expression in vivo, C57B176 IL-23p16 deficient mice
(7 mice per group) were immunized with 100 µg, of OVA emulsified in CFA. The
C57BL/6 IL-23p19 deficient mice were generated as previously described (Thakker,
P. et al., J. Immunol. (2007) 178:2589-2598). IL-6 deficient mice (B6;129S2-
Il6tm1 Kopf/J; Jackson Laboratories, five mice per group) were also immunizedto
examine how IL-6 affects IL-22 expression in vivo. Ten days after immunization,
draining inguinal lymph nodes ("LN") were harvested and restimulated in the
presence of OVA ex vivo. IL-22 concentrations were determined on day four of ex
vivo restimulation. Mice deficient in either IL-23 or IL-6 produced significantly less
IL-22 as compared to their respective WT controls (Figure 6; data representative of
at least two experiments). Thus, both IL-23 and IL-6 are required for optimal
differentiation of IL-22 expressing cells in vivo.
Example 5: IL-22 does not act on naive or differentiated T cells.
[00111] The functional receptor for IL-22 is composed of a heterodimer
complex between IL-22R1 and IL-10R2. While IL-10R2 is expressed ubiquitously in
all tissues, IL-22R1 is restricted primarily to non-lymphoid tissues and cells.
Although expression of IL-22R1 is not detected on naive or 3-day activated human
peripheral blood lymphocytes, it is not known if differentiated murine Th1, Th2, or
Th17 cells can express IL-22R1. To examine this, quantitative PCR for IL-22R1 was
performed in naive as well as differentiated DO11 cells. Expression of IL-22R1 was
not detected in naive, Th1, Th2, or Th17 T cells. In contrast, IL-22R1 was positively
detected in skin. While IL-22R1 is not expressed on T cells, it is possible that IL-22
could signal through a yet unidentified receptor. To examine functionally if IL-22 can
act on naive or differentiated T cells, naive, Th1, Th2, and Th17 T cells were
activated in the presence of IL-22. No consistent effects on proliferation and
cytokine production (IFN-?, IL-4, IL-17A) by naive or differentiated Th1, Th2, or Th17
cells were observed with addition of exogenous IL-22 up to 100 ng/ml. These data
indicate that IL-22 does not act on naive or differentiated T cells.
Example 6: IL-22 is co-expressed with IL-17A and IL-17F in vivo.
[00112] The in vitro data demonstrate that IL-22 is co-expressed with IL-17A
and IL-17F. To examine if this population exists in vivo, C57BL/6 mice were
immunized sub-cutaneously with 100 µg OVA (Sigma) emulsified in CFA (Sigma).
Seven days later, intracellular cytokine staining was performed on draining LN
directly ex vivo. Immunization with OVA/CFA increased the expansion of IL-22+
(0.34%), IL-17A+ (0.35%) and IL-17F+(0.43%) cells as compared to unimmunized
mice (Figure 7A). IL-22 was co-expressed with IL-17A (44% of IL-17A+ cells were
IL-22+) and IL-17F (45% of IL-17F cells were IL-22+) but not with IFN-?, IL-4, or IL-
10 (Figure 7B). When the expression between IL-17A and IL-17F was compared,
considerable, but not complete, co-expression was detected between the two
cytokines (Figure 7C). IL-17A+1L-17F cells comprised 60% of IL-17A+ and 70% of
IL-17F* cells. The results demonstrate heterogeneity of IL-17A and IL-17F
expression within Th17 cells. No co-expression of IL-17F with IFN-?, IL-4, or IL-10
was observed. IL-22 expression in IL-17A and/or IL-17F producing cells was also
measured and the highest IL-22 expression was found to be in IL-17A+IL-17F+ cells
(53.1%) (Figure 7C). The expression of IL-17A and IL-17F in IL-22+cells was
analyzed as well (Figure 7D). Seventy percent of IL-22+ cells expressed either IL-
17A or IL-17F, with 45% of IL-22+ cells expressing both.
[00113] The in vivo expression profiles among IL-17A, IL-17F, and IL-22 are
similar to the expression profiles generated in vitro with TGF-ß, IL-6, IL-1ß, TNF-a,
and IL-23 (See Figure 4B), suggesting that this in vitro condition is sufficient to
replicate in vivo Th17 differentiation. Similar expression patterns for IL-22, IL-17A,
and IL-17F were also observed on d4 and d10 after immunization. These data
demonstrate that IL-22 is not co-expressed with IFN-?, IL-4, and IL-10 in vivo, but
rather with IL-17A and IL-17F.
[00114] To examine if IL-23 stimulates IL-22 production from in vivo primed T
cells, LN cells were restimulated with 200 µg/ml OVA, OVA and IL-12, OVA and IL-
23, or with medium alone. IL-22 and IL-17A concentrations were examined on d4 of
restimulation. The ELISA data shown in Figure 7E are average ± SD and are
representative of three independent experiments. Addition of IL-23 enhanced the
production of IL-22 by 7 fold compared to OVA alone while exogenous IL-12 had no
effect. These data further support that IL-23, rather than IL-12, is the stimuli for
enhancing IL-22 production.
Example 7: IL-22 is expressed by human Th17 cells and, to a lesser extent,
human Thl cells.
[00115] To investigate if IL-22 is also expressed by human Th17 cells, CD4+ T
cells from six separate donors were activated with allogeneic CD4-depleted
peripheral blood lymphocytes ("PBLs") in a mixed lymphocyte reaction (MLR) under
various stimulation conditions. Human CD4+T cells were purified from peripheral
blood of donors by Rosette Sep (Stem cell technologies). In a 48 well plate, 7.5x105
human T cells were cultured with 7.5x105 irradiated (3300 rads) CD4-depleted PBLs
from a separate donor. The indicated cytokines and antibodies were added at the
following concentrations: 20 ng/ml IL-6,10 ng/ml IL-1ß, 10 ng/ml TNF-a, 1 ng/ml
TGF-ß\ 10 µg/ml anti-IL-4 (MP4-25D2, Pharmingen), 10 µg/ml anti-IFN-?(NIB412,
Pharmingen) and 10 µg/ml anti-TGF-ß (1D11, R&D Systems).
[00116] On day 7 of activation, the conditioned medium was harvested and
the human IL-22 present was quantified by coating plates with 2.5 µg/ml of anti-
human IL-22 antibody (Ab-04) and detecting with 1 µg/ml of anti-human IL-22
antibody (354A08), followed by biotinylated anti-human IgG (Pharmingen 341620)
and streptavidin HRP. Human IL-17A concentrations in the conditioned medium
were determined by ELISA coating with 4 ng/ml anti-human IL-17A (MAB317, R&D
Systems) and detecting with 75 ng/ml biotinylated anti-human IL-17A (BAF317, R&D
Systems) and streptavidin HRP. CD4+ T cells from six individual donors were
examined. In the absence of any exogenous cytokine, IL-22 was produced in low
amounts (<600 pg/ml) (Figure 8A, each line represents a distinct donor). Activation
with a Th1 condition using IL-12 and neutralizing antibody to IL-4 enhanced the
expression of IL-22 by an average of 2.5 fold. Activation with a Th17 condition using
IL-6, IL-1ß, and TNF-a resulted in greater expression of IL-22, increasing production
by an average of 17 fold. IL-17A expression was enhanced to a greater extent under
the Th17 condition (9.5 fold) than under the Th1 condition (1.4 fold) (Figure 8A).
These data indicate that, as for mouse T cells, activation of human CD4 T cells with
IL-6, IL-1ß, and TNF-a greatly increased production of both IL-22 and IL-17A.
[00117] The expression of IL-22 was also examined by intracellular cytokine
staining to determine what kind of CD4 T cells are producing IL-22 in our MLR
system. Cells activated under a Th1 differentiation condition (IL-12, anti-IL-4) or a
Th17 condition (IL-6, IL-1p, TNF-a) were restimulated with 50 ng/ml PMA, 1 µg/ml
ionomycin, and GolgiPlug (Pharmingen) for 5 hours, fixed, and permeabilized with
Cytofix/Cytoperm (Pharmingen). Intracellular co-staining of CD4+ T cells for IL-22,
IL-17A, and IFN-? was performed using anti-IL-22 PE (R&D systems), anti-IFN-?
FITC (Pharmingen), anti-CD4 PerCp-Cy5.5 (Pharmingen), and anti-IL-17A 647 (R&D
Systems). Th1 cells were defined by the expression of IFN-? and Th17 cells were
defined by their expression of IL-17A. The percentage of Th1 or Th17 cells
expressing IL-22 were calculated for each of the six donors examined. Data are
representative of at least two experiments. Although some IL-22 expression was
detected in Th1 cells, IL-22 expression was consistently higher in Th17 cells than in
Th1 cells in all six donors (Figure 8B). These data indicate that IL-22 is produced by
human Th17 cells and, to a lesser extent, by human Th1 cells.
Example 8: TGF-ß inhibits expression of IL-22 from human T cells.
[00118] Exogenous TGF-ß and IL-6 support the differentiation of Th17 cells in
mice, with IL-1ß and TNF-a further augmenting the response (Veldhoen, M. et al.,
Immunity (2006) 24:179-89; Mangan, P. R.et al., Nature (2006) 441:231-34; Bettelli,
E. et al., Nature (2006) 441:235-38). IL-22 expression from human cord blood
derived naive CD4 T cells activated with anti-CD3, anti-CD28, and IL-6 was reduced
by exogenous TGF-ß, indicating that TGF-ß is not only dispensible for human IL-22
expression, but acts to inhibit it (Zheng, Y. et al., Nature {2007) 445:648-651). To
examine the role of TGF-ß in a MLR where APCs are present, CD4+ T cells from six
donors were activated with IL-6, IL-1ß, and TNF-a alone, or further supplemented
with either exogenous TGF-ß cytokine (Sigma Aldrich) or a neutralizing antibody to
human TGF-ß (1D11, R&D Systems). IL-22 and IL-17A concentrations in day 7
conditioned media from MLR were determined. As TGF-ß can be made by
lymphocytes, addition of an anti-TGF-ß antibody is needed to prevent endogenous
TGF-ß signaling. Neutralization of TGF-ß in the context of IL-6, IL-1ß, and TNF-a
enhanced IL-22 expression by an average of 3.0 fold, indicating that TGF-ß inhibits
production of IL-22 by human T cells (Figure 9A, each line represents a distinct
donor). Consistent with this observation, exogenous TGF-ß added to IL-6, IL-1ß, and
TNF-a reduced IL-22 production by an average of 4.4 fold. The role of TGF-ß on IL-
17A expression was also examined in our human MLR system. Adding either a
neutralizing antibody to TGF-ß or the TGF-ß cytokine had no consistent effects (< 1.2
fold average change) on IL-17A production as induced by IL-6, IL-1ß, and TNF-a.
Therefore, these data demonstrate that TGF-ß inhibits IL-22 expression by PBL-
derived CD4+ human T cells, but that it has no substantial effect on IL-17A
expression.
[00119] The role of TGF-ß in regulating mouse IL-22 expression was also
examined. Naive CD62L+ D011 T cells were activated with IL-6 and with either
TGF-ß cytokine or a neutralizing antibody to TGF-ß. IL-22 expression was examined
by ELISA on day two and day four of activation. Although IL-22 expression does not
require the presence of exogenous TGF-ß, neutralization of endogenous TGF-ß with
an antibody consistently reduced expression of IL-22 (~1.8 fold) on day 2 of
activation, indicating that the presence of endogenous TGF-ß does contribute to
enhancing IL-22 production (Figure 9B) in murine T cells. By day four, neutralization
of TGF-ß did not have as large an effect on IL-22 expression, suggesting that TGF-ß
has its greatest effect on enhancing IL-22 expression during the initial activation.
Interestingly, addition of high amounts of exogenous TGF-ß (>=10 ng/ml) inhibited
IL-22 expression on both day two and day four of activation. Taken together, these
data indicate that in the presence of IL-6, endogenous TGF-ß signaling enhances
mouse IL-22 production during initial stages of activation whereas addition of large
amounts of exogenous TGF-ß actually inhibits IL-22 expression.
Example 9: IL-22 administration via adenoviral vectors effects an acute phase
response in mice.
[00120] IL-22 expression by both mouse and human T cells can be induced
by IL-6, IL-1ß, and TNF-a. These pro-inflammatory cytokines are known to induce
an acute phase response. An acute phase response is a collection of biochemical,
physiologic, and behavioral changes indicative of an inflammatory condition. The
modulation of specific proteins known as acute phase reactants is a biochemical
hallmark of an acute phase response and of inflammation. Treatment of hepatocytes
with IL-22 in vitro and administration of IL-22 in vivo can rapidly induce the
expression of serum amyloid A (SAA), a major acute phase reactant (Dumoutier, L.
et al., Proc. Nat'l Acad. Sci. U.S.A. (2000) 97:10144-49; Wolk, K. et al., Immunity
(2004)21:241-54).
[00121] To study the role of IL-22 in a more chronic setting, IL-22 was
ectopically expressed in C57BL/6 mice using a replication-defective adenovirus.
Expression of acute phase reactants was examined up to two weeks after
administration. SAA expression was significantly enhanced as compared to GFP-
expressing adenovirus starting on day three and remained significantly increased up
to 14 days later (data not shown). Fibrinogen, another acute phase reactant, was
also significantly enhanced in mice administered the IL-22 expressing adenovirus,
starting as early as day one and remaining significant up to seven days later (data
not shown). Whereas some proteins are induced during an acute phase response,
other proteins, such as albumin, are decreased during inflammation. Mice treated
with IL-22 expressing adenovirus exhibited decreased expression of albumin as
compared to the GFP expressing control (data not shown). These data demonstrate
that exposure to IL-22 for two weeks using an adenovirus for ectopic expression
results in the modulation of several proteins indicative of an acute phase response.
[00122] The effects of IL-22 adenoviral administration on blood cells were also
investigated. Mice treated with the IL-22 expressing adenovirus resulted in a
significant increase in serum platelet seven days (1. 5 fold) and 14 days (2.0 fold)
after viral inoculation relative to the GFP adenoviral control (data not shown).
Concomitant with this increase in platelet number, a mild anemia indicated by a
modest, but statistically significant decrease in red blood cells was observed.
Similarly significant decreases were also detected in both the serum hematocrit and
hemoglobin (data not shown). A trend of increased numbers of segmented
neutrophils in the blood was also found, although the increase was not always
significant. Taken together, the biochemical and hematological changes we
observed in mice treated with an IL-22 expressing adenovirus indicate that IL-22
induces an acute phase response (APR) in vivo.
Example 10: IL-22 protein can directly enhance SAA in the absence of IL-6.
[00123] Our data using adenoviral constructs demonstrated that IL-22 is
capable of modulating parameters indicative of an acute phase response in vivo.
However, it was possible that IL-22 was acting with other factors as a result of
infection with adenovirus. To directly examine the role of IL-22, IL-22 protein was
administered to mice by intraperitoneal injection and the serum was examined at
several timepoints for changes in acute phase reactants. Mice were administered 25
µg of IL-22 protein or PBS via intraperitoneal injection. Mouse IL-22 was generated
using methods previously described (Li, J., et al., Int. Immunopharmacol. (2004)
4:693-708). Blood and liver were harvested at 0.5, 1, 3, 6, and 24 hours and serum
prepared. SAA was quantified using a SAA-specific ELISA (Invitrogen).
Administration of IL-22 protein was sufficient to significantly enhance expression of
SAA protein in the serum starting at 3 hours after administration and up to 24 hours
(Figure 10A).
[00124] Livers from the mice administered IL-22 or PBS were also snap
frozen and then processed for RNA using the Ribopure RNA isolation kit (Ambion).
Quantitative PCR was performed using Taqman (Applied Biosystems) and pre-
qualified primer/probes (Applied Biosystems) for SAA1, fibrinogen, haptoglobin, and
albumin. The relative amounts of each gene, as normalized to p2 microglobulin,
were then calculated. SAA transcript expression in the liver was increased by 0.5
hour after administration and was significantly increased at one hour and three hours
(Figure 10B). In addition to SAA, IL-22 was observed to significantly enhance
fibrinogen transcripts in the liver within 1 hour after injection (Figure 10B).
Haptoglobin and albumin transcripts were not statistically changed at up to 3 hours
after injection (Figure 10B). Thus, IL-22 can begin to effect changes of an acute
phase response within 1 hour after intraperitoneal administration.
[00125] Although IL-22 injection induced SAA, it was possible that IL-22 was
acting indirectly by inducing other cytokines such as IL-6 and TNF-a that then
directly enhanced SAA expression. To examine if IL-22 induces IL-6 and TNF-a in
vivo, serum IL-6 and TNF-a expression was examined after IL-22 adminstration.
Concentrations of IL-6 and TNF-a were determined using the Inflammation CBA kit
(Pharmingen). No significant changes were observed up to 24 hours post
administration (Figure 10C). As it was possible that the amounts of IL-6 or TNF-a
produced were too low to be detected, IL-22 protein was also directly administered to
IL-6 deficient mice. C57BL/6 and C57BL/6 IL-6-/- mice were administered 25 µg of
IL-22 via intraperitoneal injection. Mice were bled at six hours after injection and
SAA quantified from the serum. Fifteen mice were examined per group, and the
data shown are representative of at least two experiments. The absence of IL-6 had
no effects on IL-22-induced SAA production (Figure 10D) in IL-6 deficient mice.
Taken together, these data support earlier studies showing that IL-22 modulates
parameters indicative of an acute phase response. These data further indicate that
IL-22 can regulate SAA, a major acute phase reactant, in the absence of IL-6
signaling.
Examle 11: IL-22 induces neutrophil mobilization in the blood.
[00126] The hematological changes that result from IL-22 protein
administration were also examined. Mice were administered 25 µg of IL-22 protein
or PBS via intraperitoneal injection. Blood was collected at several timepoints after
administration and neutrophil numbers quantified using a Cell-Dyn hematology
analyzer (Abbott Diagnostics). IL-22 induced a significant, two fold increase in
neutrophil counts in the blood one hour after administration (Figure 11 A). This
increase was transient as no statistically significant changes were observed after
one hour. Expression of several neutrophil chemoattractants was also examined. A
significant increase in CXCL1 (13 fold) was detected in the serum at one hour after
administration (Figure 11B). CXCL1 was quantified using a CXCL1 -specific ELISA
(R&D Systems) following the manufacturer's directions. Quantitative PCR revealed
that CXCL1 transcripts in the liver were also significantly enhanced starting at 0.5
hour after injection (Figure 11C). Data are representative of at least three
experiments. No increases in CXCL2, CXCL5, or G-CSF were observed in the
serum at any timepoint. These data demonstrate that IL-22 can induce neutrophil
mobilization and the expression of the neutrophil chemoattractant, CXCL1, possibly
from the liver.
Example 12: IL-22, IL-17A, and IL-17F cooperatively induce anti-microbial
peptides.
[00127] One function of IL-22 is to enhance the expression of anti-microbial
peptides associated with host defense, including beta-defensin 2 (hBD-2), S100A7,
S100A8, and S100A9 (Wolk et al., Immunity (2004) 21:241-54; Boniface et al., J.
Immunol. (2005) 174:3695-3702). To examine whether IL-17A, IL-17F, and IL-22
can act cooperatively to regulate these genes, primary human keratinocytes were
treated with IL-22, IL-17A, IL-17F, or with combinations of these cytokines.
Specifically, primary human keratinocytes (ScienCell) were cultured in keratinocyte
medium (ScienCell) on human fibrinogen coated plates (BD Biosciences). Cells
were passaged at 80% confluency and all experiments were done between
passages 2-4. For evaluation of cytokine effects, 15,000 cells were seeded into a 24
well plate and allowed to adhere for 48 hrs. Cells were then treated with human IL-
22, IL-17A, and IL-17F for 44 hours. RNA was purified and quantitative PCR
performed using Taqman Real Time PCR and pre-qualified primer-probes (Applied
Biosystems). Relative amounts of hBD-2, S100A7, S100A8, and S100A9 transcript
were determined by normalization to GAPDH. Fold induction was calculated relative
to expression in keratinocytes that were not treated with any cytokine (denoted by
dashed line in Figure 12). IL-17A induced upregulation of all four anti-microbial
peptides examined (5-70 fold induction at 200 ng/ml) (Figure 12A). IL-22 also
induced all four anti-microbial proteins (2-5 fold induction at 200 ng/ml) whereas IL-
17F (200 ng/ml) induced hBD-2 by 8 fold, S100A8 by 1.5 fold, and S100A9 by 2 fold
but did not upregulate S100A7.
[00128] Keratinocytes were then cultured with paired combinations of IL-22,
IL-17A, and IL-17F. Human keratinocytes were stimulated with pairwise
combinations of IL-22 (200 ng/ml), IL-17A (20 ng/ml), and IL-17F(20 ng/ml) for 44
hours. hBD-2, S100A7, S100A8, and S100A9 mRNA were quantitated as described
above. Data are average ± SD and are representative of experiments performed on
three separate donors. Treatment with IL-22 (200 ng/ml) and IL-17A (20 ng/ml) led
to a synergistic increase of hBD-2 (IL-22: 5 fold; IL-17A: 60 fold; IL-22+IL-17A: 180
fold) and S100A9 (IL-22: 2 fold; IL-17A: 5 fold; IL-22+IL-17A: 13 fold) (Figure 12B).
Treatment with IL-22 (200 ng/ml) and IL-17F (20 ng/ml) also synergistically
enhanced hBD-2 (IL-22: 5 fold; IL-17F: 2 fold; IL-22+IL-17F: 20 fold). Even though
S100A7, S100A8, and S100A9 were not upregulated by IL-17F (20 ng/ml) alone, IL-
17F plus IL-22 enhanced the expression of these three peptides by 2 fold over IL-22
alone. These data demonstrate that IL-22 can act cooperatively, either
synergistically or additively, with IL-17A or IL-17F. Keratinocytes treated with a
combination of IL-17A and IL-17F enhanced S100A8, but did not further enhance
expression of hBD-2, S100A7, or S100A9. The combination of IL-17A and IL-17F
resulted in less induction of these genes than the combination of IL-22 with IL-17A or
IL-17F. Expression of receptors for IL-22 (IL-22R1) or IL-17 (IL-17RA) were not
altered with IL-22, IL-17A, or IL-17F treatment, suggesting that these effects are not
related to changes in receptor expression. These data demonstrate that IL-22 in
combination with IL-17A or IL-17F cooperatively enhances the expression of anti-
microbial peptides.
Example 13: IL-22, IL-17A, IL-17F, and IL-23p19 are upregulated in psoriasis.
[00129] The data demonstrate that IL-22 is co-expressed with IL-17A and IL-
17F in vivo after immunization with a model antigen. To further examine the
relevance of these findings in a human disease, the expression of IL-22, IL-17A, IL-
17F, and IL-23p19 were analyzed in psoriasis vulgaris, an inflammatory disease of
the skin. Psoriasis is a complex, multigenic disease that affects approximately 2% of
the US population and is characterized by the formation of red, raised, scaly lesions
(Schon, M. et al., N. Engl J. Med. (2005) 352:1899-1912). While the etiology of
psoriasis is still being debated, considerable evidence exists showing that T cells are
a pathogenic component of this disease (Christophers, E. et al., Int. Arch. Allergy
Immunol. (1996) 110:199-206). T cells are present in lesional skin of psoriasis
patients and a variety of T cell derived cytokines have been found to be upregulated
in lesional skin (Nickoloff, B. et al., Arch. Dermatol. (1991) 127:871-884). Here, the
expression of IL-22, IL-17A, IL-17F, and IL-23p19 was examined in skin from
psoriasis patients and the potential correlative expression between these genes was
analyzed.
[00130] Paired biopsies of non-lesional and lesional skin were obtained from
46 patients with active psoriasis and relative concentrations of IL-22, IL-17A, IL-17F,
and IL-23p19 determined by quantitative PCR (Figure 13A). In non-lesional skin, IL-
22 was below the level of detection in 31 of 46 patients. IL-22 was significantly
upregulated an average of 25 fold in lesional skin as compared to non-lesional skin
(p= 7 x10-9), with all 46 patients upregulating IL-22. IL-17A was not detected in 26 of
46 non lesional skin biopsies but was also significantly upregulated 19 fold (p=1x10-
16), with 45 out of 46 patients upregulating IL-17A. In 32 of 46 patients, IL-17F was
below the level of detection in non-lesional skin. IL-17F was upregulated 21.4 fold
(p=4x10-10) with 45 of 46 patients having higher levels of IL-17F in lesional skin.
Expression of IL-23p19 was enhanced by 11 (p<0.0001) fold in lesional skin as
compared to non-lesional skin, with 44 of 46 patints upregulating IL-23p19. Values
were determined by paired Student's t test.
[00131] These data are consistent with previous reports demonstrating IL-22
and IL-17A are upregulated in lesional skin of psoriasis patients (Wolk, K. et al.,
Immunity (2004) 21:241-254; Wolk, K. et al., Eur. J. Immunol. ( 2006) 36(5): 1309-23;
Li, J. et al., J. Huazhong Univ. Sci. Technolog. Med. Sci. (2004) 24:294-296)
However, in this study a larger number of patients was analyzed and IL-17A was
also examined by quantitative PCR as opposed to the semi-quantitative method
used previously. Furthermore, IL-17F, whose expression was previously
uncharacterized in psoriasis, is also significantly upregulated in lesional skin. These
results suggest that Th17 cytokines play a role in the pathogenesis of psoriasis.
[00132] IL-22, IL-17A, IL-17F, and IL-23 were also examined for any
correlation in their relative concentrations by performing a Spearman's rank
correlation analysis (Figure 13B). IL-22 exhibited a positive, but not significant,
correlation with IL-17A. In contrast, a positive and significant correlation was
obtained between IL-22 and IL-17F (0.37, p=0.01) and between IL-17A and 1L-17F
(0.44, p = 0.003). These positive correlation coefficients suggest that there is a
correlative relationship between IL-22 and IL-17F and between IL-17A and IL-17F.
While the data demonstrate that IL-22 is co-expressed with both IL-17A and IL-17F
in vivo in CD4+ T cells, expression of these cytokines is not restricted to just
lymphocytes. In addition to T cells, IL-17A mRNA has also been detected in
neutrophils, eosinophils, and monocytes while IL-22 mRNA is also found in NK cells
(Molet, S. et al., J. Allergy Clin. Immunol. (2001)108:430-438.; Ferretti, S. et al., J.
Immunol. (2003) 170:2106-2112.; Awane, M. et al., J. Immunol. (1999) 162:5337-
5344.; Wolk, K. et al., Immunity (2004) 21:241-254). Because neutrophils,
monocytes, and NK cells have been reported to be present in lesional skin (Schon,
M. et al. 2005. N. Engl J. Med. 352:1899-1912), these cells types could also be
contributing to the overall IL-22 and IL-17A mRNA in the skin and therefore affect our
correlation analysis, especially between IL-22 and IL-17A. However, the positive
and significant correlations obtained between IL-22 and IL-17F, as well as between
IL-17A and IL-17F, demonstrate a directly proportional relationship between these
cytokines in psoriasis. A positive and significant correlation was also detected
between IL-23 and IL-17A as well as IL-23 and IL-17F.
Example 14: Model for Treatment of Psoriasis
[00133] Xenogeneic transplantation in SCID mice is a recognized model for
studying psoriasis, see e.g., Boehncke et al., Br. J. Dermatol. (2005) 153(4):758-66.
Under local anesthesia, lesional split-skin (thickness about 0.5 mm) is excised from a
patient with chronic plaque-stage psoriasis. Human split grafts are transplanted on
the back of 6-8 week old SCID mice. Mice are given 3 weeks to accept the graft and
heal. At 22 days following transplantation, mice are injected intraperitoneally with a
composition comprising an antagonist of IL-17F alone or an antagonist of IL-22, and
at least one IL-17A, IL-17F, or IL-23 antagonist, every other day. As a negative
control, mice receive daily intragastric applications of 200 uL PBS and/or isotype
control antibody. As a positive control, mice receive daily intragastric application of 2
mg kg-1 dexamethasone in 200 uL PBS. The negative controls develop hallmarks of
psoriasis, including acanthosis, papillomatosis, parakeratosis, and a dense
mononuclear infiltrate. Mice are sacrificed at day 50 following transplantation and
the grafts with surrounding skin are excised. One half of the graft is fixed in formalin
and the other half is frozen in liquid nitrogen. Routine hematoxylin and eosin
stainings are performed and the pathological changes of the grafts are analyzed both
qualitatively (epidermal differentiation) and quantitatively (epidermal thickness,
inflammatory infiltrate). The mean epidermal thickness may be measured from the
tip of the rete ridges to the border of the viable epidermis using an ocular
micrometer. The density of the inflammatory infiltrate may be determined by
counting the number of cells in three adjacent power fields. Disease progression
may be evaluated using histological analysis to measure hallmarks of psoriasis, such
as acanthosis, papillomatosis, parakeratosis, inflammatory infiltrates, and the
appearance of the corneal and granular layers.
[00134] Negative control mice injected with 200 uL PBS or an isotype-
matched control antibody following graft transplantation progressively develop
psoriasis. Because psoriatic lesions express higher levels of IL-22, IL-17A, IL-17F,
and IL-23p19, treatment with an antagonist of IL-22 and an antagonist of at least one
of IL-17A, IL-17F, or IL-23 is expected to suppress or delay psoriasis. Thus, since
this model predicts treatment efficacy for psoriasis, treatment with an antagonist of
IL-17F alone or an antagonist of IL-22 in combination with an antagonist of at least
one of IL-17A, IL-17F, or IL-23 is expected to suppress or delay psoriasis in humans.
Example 15: Treatment of Patients
[00135] Patients with an autoimmune disorder, respiratory disorder,
inflammatory condition of the skin, cardiovascular system, nervous system, kidneys,
liver and pancreas or transplant patients may be treated with an antagonist of IL-22
and an antagonist of at least one of IL-17A, IL-17F, or IL-23. Exemplary treatment
regimens and expected outcomes are provided below. Dosages and frequency may
be adjusted as necessary.
Table 1: Treatment Regimens
[00136] In Table 1, the anti-IL-22 antibody can be replaced with a soluble IL-
22 receptor or binding protein. The anti-IL-17A antibody in Table 1 can be replaced
with an anti-IL-23 antibody, an anti-IL-17F antibody, or a soluble receptor or binding
protein for IL-17A, IL-17F, of IL-23.
[00137] IL-22 has been characterized as a Th1 cytokine because IL-22 mRNA
was found to be upregulated by IL-12 (Wolk et al., J. Immunol. (2002) 168:5397-
5402). The work described in this application shows that IL-22 protein is aJso
expressed in the Th17 lineage, revealing a new effector cytokine from Th17 cells.
Despite being a Th17 cytokine, IL-22 is located ~90kb away from IFN-?. The distinct
expression between IL-22 and IFN-? suggests cis-regulatory elements exist within
this locus that may regulate the differentiation of Th1 versus Th17 cells.
[00138] These data also define a new function for IL-23 in inducing IL-22
expression. Although IL-17A is an effector cytokine downstream of IL-23, certain
data suggests that IL-17A may not account for all the functions of IL-23. For
example, IL-23p19 deficient mice are completely resistant to disease in CIA (Murphy
et al., J. Exp. Med. (2003) 198:1951-57). IL-17A deficient mice remain susceptible,
albeit with a significantly reduced incidence and severity (Nakae et al., J. Immunol.
(2003) 171:6173-77. Also, IL-23p19 deficient mice are susceptible to Citrobacter
rodentium infection despite maintaining wild-type expression of IL-17A (Mangan et
al., Nature (2006) 441:231-34. These data suggest other cytokines downstream of
IL-23 are involved.
[00139] IL-22 is upregulated in at least rheumatoid arthritis, psoriasis, and
inflammatory bowel disease (Wolk et al., Immunity (2004) 21:241-54; Ikeuchi et al.,
Arthritis Rheum. (2005) 52:1037-46; Andoh et al., Gastroenterology (2005) 129:969-
84). Similar to IL-17A and IL-17F, IL-22 acts directly on epithelial and fibroblast cells
in peripheral tissues (Wolk et al., Immunity (2004) 21:241-54; Ikeuchi et al., Arthritis
Rheum. (2005) 52:1037-46; Kolls, J.K., and A. Linden. Immunity (2004) 21:467-476.
The data demonstrate that IL-22 can function in synergy with IL-17A or IL-17F to
enhance the expression of anti-microbial peptides, suggesting that these cytokines
cooperate to protect against infection.
[00140] The specification is most thoroughly understood in light of the
teachings of the references cited within the specification. The embodiments within
the specification provide an illustration of embodiments of the invention and should
not be construed to limit the scope of the invention. The skilled artisan readily
recognizes that many other embodiments are encompassed by the invention. All
publications and patents cited in this disclosure are incorporated by reference in their
entirety. To the extent the material incorporated by reference contradicts or is
inconsistent with this specification, the specification will supersede any such
material. The citation of any references herein is not an admission that such
references are prior art to the present invention.
[00141] Unless otherwise indicated, all numbers expressing quantities of
ingredients, reaction conditions, and so forth used in the specification, including
claims, are to be understood as being modified in all instances by the term "about."
Accordingly, unless otherwise indicated to the contrary, the numerical parameters
are approximations and may vary depending upon the desired properties sought to
be obtained by the present invention. At the very least, and not as an attempt to limit
the application of the doctrine of equivalents to the scope of the claims, each
numerical parameter should be construed in light of the number of significant digits
and ordinary rounding approaches.
[00142] Unless otherwise indicated, the term "at least" preceding a series of
elements is to be understood to refer to every element in the series. Those skilled in
the art will recognize, or be able to ascertain using no more than routine
experimentation, many equivalents to the specific embodiments of the invention
described herein. Such equivalents are intended to be encompassed by the
following claims.
CLAIMS
We claim:
1. A method of treating a disorder associated with IL-22, and at least one of IL-
17A, IL-17F, or IL-23, in a subject, comprising, administering to the subject a
therapeutically effective amount of a composition comprising an antagonist of
IL-22, and an antagonist of at least one of IL-17A, IL-17F, or IL-23.
2. The method of claim 1, wherein the antagonist of IL-22 is an antibody or
antigen-binding fragment thereof and the antagonist of at least one of IL-17A,
IL-17F, or IL-23 is an antibody or antigen-binding fragment thereof.
3. The method of claim 1, wherein the antagonist of IL-22 is a soluble receptor or
a binding protein and the antagonist of at least one of IL-17A, IL-17F, or IL-23
is an antibody or antigen-binding fragment thereof.
4. The method of claim 1, wherein the antagonist of IL-22 is an antibody or
antigen-binding fragment thereof and the antagonist of at least one of IL-17A,
IL-17F, or IL-23 is a soluble receptor or a binding protein.
5. The method of any one of claims 1 -4, wherein the disorder is chosen from
psoriasis, rheumatoid arthritis, juvenile rheumatoid arthritis, osteoarthritis,
psoriatic arthritis, ankylosing spondylitis, systemic lupus erythematosis,
multiple sclerosis, inflammatory bowel disease, pancreatitis, and Crohn's
disease.
6. The method of any one of claims 1 -5, further comprising administering to the
subject another therapeutic agent chosen from a cytokine inhibitor, a growth
factor inhibitor, an immunosuppressant, an anti-inflammatory agent, a
metabolic inhibitor, an enzyme inhibitor, a cytotoxic agent, and a cytostatic
agent.
7. The method of claim 6, wherein the therapeutic agent is chosen from a TNF
antagonist, an IL-12 antagonist, an IL-15 antagonist, an IL-18 antagonist, an
IL-21 antagonist, a T cell depleting agent, a B cell depleting agent,
methotrexate, leflunomide, sirolimus (rapamycin) or an analog thereof, a Cox-
2 inhibitor, a cPLA2 inhibitor, an NSAID, and a p38 inhibitor.
8. The method of any one of claims 1 -7, wherein the subject is a human.
9. The method of any one of claims 1 -8, wherein the disorder is psoriasis.
10. The method of claim 1, wherein the disorder is psoriasis and wherein the
composition comprises an antibody or antigen-binding fragment thereof that
binds IL-22 and an antibody or antigen-binding fragment thereof that binds IL-
17A or lL-17F.
11. The method of claim 1, wherein the disorder is arthritis and wherein the
composition comprises an antibody or antigen-binding fragment thereof that
binds IL-22 and an antibody or antigen-binding fragment thereof that binds IL-
17A or lL-17F.
12. The method of claim 1, wherein the disorder is rheumatoid arthritis and
wherein the composition comprises an antibody or antigen-binding fragment
thereof that binds IL-22 and an antibody or antigen-binding fragment thereof
that binds IL-17A or IL-17F.
13. The method of claim 1, wherein the disorder is inflammatory bowel disease
and wherein the composition comprises an antibody or antigen-binding
fragment thereof that binds IL-22 and an antibody or antigen-binding fragment
thereof that binds IL-17A or IL-17F.
14. The method of claim 1, wherein the disorder is Crohn's disease and wherein
the composition comprises an antibody or antigen-binding fragment thereof
that binds IL-22 and an antibody or antigen-binding fragment thereof that
binds IL-17A or IL-17F.
15. A method of inducing an anti-microbial peptide in a mammalian cell,
comprising administering to the mammalian cell IL-22 and IL-17A, IL-22 and
IL-17F, or IL-22, IL-17A, and IL-17F in an amount effective to induce an anti-
microbial peptide in the mammalian cell.
16. The method of claim 15, wherein the mammalian cell is a keratinocyte.
17. The method of claim 15 or 16, wherein the antimicrobial peptide is hBD-2,
S100A7, S100A8, or S100A9.
18. A method for detecting the presence of IL-22 and at least one of IL-17A, IL-
17F, or IL-23 in a sample, in vitro, comprising contacting the sample with a
first reagent that binds to IL-22 and a second reagent that binds to IL-17A, IL-
17F, or IL-23, and detecting formation of a first complex between the first
reagent and the sample and a second complex between the second reagent
and the sample, wherein detection of the first complex is indicative of the
presence of IL-22 in the sample and detection of the second complex is
indicative of the presence of at least one of IL-17A, IL-17F, or IL-23 in the
sample.
19. The method of claim 18, wherein the first reagent is a labeled antibody.
20. The method of claim 19, wherein the second reagent is a labeled antibody.
21. The method of any one of claims 18-20, wherein the sample comprises cells.
22. The method of claim 21, wherein the amount of the first complex detected is
proportional to the amount of intracellular IL-22 and the amount of the second
complex detected is proportional to the amount of intracellular IL-17A, IL-17F,
or IL-23.
The present application provides methods of modulating immune responses by using IL-22 in combination with at
least one of IL-17A, IL-17F, or IL-23 or by using an IL-22 antagonist, such as an antibody or a soluble receptor or a binding protein,
in combination with an antagonist of at least one of IL-17A, IL-17F, or IL-23