The present invention relates to novel antibodies capable of binding specifically to the human c-Met receptor and/or capable of specifically inhibiting the tyrosine kinase activity of said receptor, especially monoclonal antibodies of murine, chimeric and humanized origin, as well as the amino acid and nucleic acid sequences coding for these antibodies. More particularly, antibodies according to the invention are capable of inhibiting the c-Met dimerization. The invention likewise comprises the use of these antibodies as a medicament for the prophylactic and/or therapeutic treatment of cancers or any pathology connected with the overexpression of said receptor as well as in processes or kits for diagnosis of illnesses connected with the overexpression of c-Met. The invention finally comprises products and/or compositions comprising such antibodies in combination with other antibodies and/or chemical compounds directed against other growth factors involved in tumor progression or metastasis and/or compounds and/or anti-cancer agents or agents conjugated with toxins and their use for the prevention and/or the treatment of certain cancers.

BACKGROUND OF THE INVENTION
Receptor tyrosine kinase (RTK) targeted agents such as trastuzumab, cetuximab, bevacizumab, imatinib and gefitinib inhibitors have illustrated the interest of targeting this protein class for treatment of selected cancers.
c-Met, is the prototypic member of a sub-family of RTKs which also includes RON and SEA. The c-Met RTK family is structurally different from other RTK families and is the only known high-affinity receptor for hepatocyte growth factor (HGF), also called scater factor (SF) [D.P. Bottaro et al, Science 1991, 251 : 802-804; L. Naldini et al, Eur. MoI. Biol. Org. J. 1991, 10:2867-2878]. c-Met and HGF are widely expressed in a variety of tissue and their expression is normally restricted to cells of epithelial and mesenchymal origin respectively [M. F. Di Renzo et al., Oncogene 1991, 6:1997-2003; E. Sonnenberg et al., J. Cell. Biol. 1993, 123:223-235]. They are both required for normal mammalian development and have been shown to be particularly important in cell migration, morphogenic differentiation, and organization of the three-dimensional tubular structures as well as growth and angiogenesis [F. Baldt et al., Nature 1995, 376:768-771; C. Schmidt et al., Nature. 1995:373:699-702; Tsarfaty et al., Science 1994, 263:98-101]. While the controlled regulation of c-Met and HGF have been shown to be important in mammalian development, tissue maintenance and repair [Nagayama T, Nagayama M, Kohara S, Kamiguchi H, Shibuya M, Katoh Y, Itoh J, Shinohara Y., Brain Res. 2004, 5;999(2): 155-66; Tahara Y, Ido A, Yamamoto S, Miyata Y, Uto H, Hori T, Hayashi K, Tsubouchi H., J Pharmacol Exp Ther. 2003, 307(1): 146-51], their dysregulation is implicated in the progression of cancers.
Aberrant signalling driven by inappropriate activation of c-Met is one of the most frequent alteration observed in human cancers and plays a crucial role in tumorigenesis and metastasis [Birchmeier et al., Nat. Rev. MoI. Cell Biol. 2003, 4:915-925; L. Trusolino and Comoglio P. M., Nat Rev. Cancer. 2002, 2(4):289-300].
Inappropriate c-Met activation can arise by ligand-dependent and independent mechanisms, which include overexpression of c-Met, and/or paracrine or autocrine activation, or through gain in function mutation [J.G. Christensen, Burrows J. and Salgia R., Cancer Latters. 2005, 226:1-26]. However an oligomerization of c-Met receptor, in presence or in absence of the ligand, is required to regulate the binding affinity and binding kinetics of the kinase toward ATP and tyrosine-containing peptide substrates [Hays JL, Watowich SJ, Biochemistry, 2004 Aug 17, 43:10570-8]. Activated c-Met recruits signalling effectors to its multidocking site located in the cytoplasm domain, resulting in the activation of several key signalling pathways, including Ras-MAPK, PI3K, Src and Stat3 [Gao CF, Vande Woude GF, Cell Res. 2005, 15(1):49-51; Furge KA, Zhang YW, Vande Woude GF, Oncogene. 2000, 19(49):5582-9]. These pathways are essential for tumour cell proliferation, invasion and angiogenesis and for evading apoptosis [Furge KA, Zhang YW, Vande Woude GF, Oncogene, 2000, 19(49):5582-9; Gu H, Neel BG, Trends Cell Biol. 2003 Mar, 13(3): 122-30; Fan S, Ma YX, Wang JA, Yuan RQ, Meng Q, Cao Y, Laterra JJ, Goldberg ID, Rosen EM, Oncogene. 2000 Apr 27, 19(18):2212-23]. In addition, a unique facet of the c-Met signalling relative to other RTK is its reported interaction with focal adhesion complexes and non kinase binding partners such as Cc6β4 integrins [Trusolino L, Bertotti A, Comoglio PM, Cell. 2001, 107:643-54], CD44v6 [Van der Voort R, Taher TE, Wielenga VJ, Spaargaren M, Prevo R, Smit L, David G, Hartmann G, Gherardi E, Pals ST, J Biol Chem. 1999, 274(10):6499-506], Plexin Bl or semaphorins [Giordano S, Corso S, Conrotto P, Artigiani S, Gilestro G, Barberis D, Tamagnone L, Comoglio PM, Nat Cell Biol. 2002, 4(9):720-4; Conrotto P, Valdembri D, Corso S, Serini G, Tamagnone L, Comoglio PM, Bussolino F, Giordano S, Blood. 2005, 105(11):4321-9; Conrotto P, Corso S, Gamberini S, Comoglio PM, Giordano S, Oncogene. 2004, 23:5131-7] which may further add to the complexity of regulation of cell function by this receptor. Finally recent data demonstrate that c-Met could be involved in tumor resistance to gefϊtinib or erlotinib suggesting that combination of compound targeting both EGFR and c-Met might be of significant interest [Engelman JA at al., Science, 2007, 316:1039-43].
In the past few years, many different strategies have been developed to attenuate c-Met signalling in cancer cell lines. These strategies include i) neutralizing antibodies against c-Met or HGF/SF [Cao B, Su Y, Oskarsson M, Zhao P, Kort EJ, Fisher RJ, Wang LM, Vande Woude GF, Proc Natl Acad Sci U S A. 2001, 98(13):7443-8; Martens T, Schmidt NO, Eckerich C, Fillbrandt R, Merchant M, Schwall R, Westphal M, Lamszus K, Clin Cancer Res. 2006, 12(20):6144-52] or the use of HGF/SF antagonist NK4 to prevent ligand binding to c-Met [Kuba K, Matsumoto K, Date K, Shimura H, Tanaka M, Nakamura T, Cancer Res., 2000, 60:6737-43], ii) small ATP binding site inhibitors to c-Met that block kinase activity [Christensen JG, Schreck R, Burrows J, Kuruganti P, Chan E, Le P, Chen J, Wang X, Ruslim L, Blake R, Lipson KE, Ramphal J, Do S, Cui JJ, Cherrington JM, Mendel DB, Cancer Res. 2003, 63:7345-55], iii) engineered SH2 domain polypeptide that interferes with access to the multidocking site and RNAi or ribozyme that reduce receptor or ligand expression. Most of these approaches display a selective inhibition of c-Met resulting in tumor inhibition and showing that c-Met could be of interest for therapeutic intervention in cancer.
Within the molecules generated for c-Met targeting, some are antibodies.
The most extensively described is the anti-c-Met 5D5 antibody generated by Genentech [WO96/38557] which behaves as a potent agonist when added alone in various models and as an antagonist when used as a Fab fragment. A monovalent engineered form of this antibody described as one armed 5D5 (OA5D5) and produced as a recombinant protein in E. CoIi is also the subject of a patent application [WO2006/015371] by Genentech. However, this molecule that could not be considered as an antibody because of its particular scarfold, displays also mutations that could be immunogenic in humans. In terms of activity, this unglycosylated molecule is devoided of effector functions and finally, no clear data demonstrate that OA5D5 inhibits dimerization of c-Met. Moreover, when tested in the G55 in vivo model, a glioblastoma cell line that expresses c-Met but not HGF mRNA and protein and that grows independently of the ligand, the one armed anti-c-Met had no significant effect on G55 tumor growth suggesting that OA5D5 acts primarily by blocking HGF binding and is not able to target tumors activated independently of HGF [Martens T. et al, Clin. Cancer Res., 2006, 12(20):6144-6152].
Another antibody targeting c-Met is described by Pfizer as an antibody acting "predominantly as c-Met antagonist, and in some instance as a c-Met agonist" [WO 2005/016382]. No data showing any effect of Pfizer antibodies on c-Met dimerization is described in this application.
One of the innovant aspects of the present invention is to generate mouse monoclonal antibodies without intrinsic agonist activity and inhibiting c-Met dimerization. In addition of targeting ligand-dependent tumors, this approach will also impair ligand- independent activations of c-Met due to its overexpression or mutations of the intra cellular domains which remained dependent to oligomerization for signalling. Another aspect of the activity of such antibodies could be a steric hindrance for c-Met interaction with its partners that will result in impairment of c-Met functions. These antibodies will be humanized and engineered preferentially, but not limited, as human IgGl to get effector functions such as ADCC and CDC in addition to functions linked to the specific blockade of the c-Met receptor.

DISCLOSURE OF THE INVENTION
Surprisingly, for the first time, inventors have managed to generate an antibody capable of binding to c-Met but also capable of inhibiting the c-Met dimerization. If it is true that, in the prior art, it is sometimes suggested that an antibody capable of inhibiting the dimerization of c-Met with its partners could be an interesting one, it has never been disclosed, or clearly suggested, an antibody capable of doing so. Moreover, regarding antibody specificity, it was not evident at all to succeed in the generation of such an active antibody.
In a first aspect, a subject of the present invention is a process for the generation and the selection of antibodies according to the invention.
More particularly, the invention concerns a process for the selection of an anti c- Met antibody, or one of its functional fragments or derivatives, capable to inhibit both ligand-dependent and ligand-independent activation of c-Met, said process comprising the following steps:
i) screening the generated antibodies and selecting antibodies capable to bind specifically to c-Met;
ii) evaluating in vitro the selected antibodies of step i) and selecting antibodies capable to inhibit at least 50 %, preferably at least 60 %, 70 % or 80 % of tumoral cell proliferation for at least one tumor type; and then
iii) testing the selected antibodies of step ii) and selecting antibodies capable to inhibit the c-Met dimerization.
As it was explained before, the inhibition of the c-Met dimerization is a capital aspect of the invention as such antibodies will present a real interest for a larger population of patients. Not only ligand-dependent activated c-Met cancer, as it was the case until the present invention, but also ligand-independent activated c-Met cancer could be treated with antibodies generated by the process of the present invention.
The generation of the antibody can be realized by any method known by the man skilled in the art, such as for example, fusion of a myeloma cell with spleen cells from immunized mice or other species compatible with the selected myeloma cells [Kohler & Milstein, 1975, Nature, 256:495-497]. The immunized animals could include transgenic mice with human immunoglobulin loci which then directly produce human antibodies. Another possible embodiment could consist in using phage display technologies to screen libraries.
The screening step i) can be realized by any method or process known by the man skilled in the art. As non limitative examples, can be mentioned ELISA, BIAcore, immunohistochemistry, FACS analysis and functional screens. A preferred process consists in a screen by ELISA on the c-Met recombinant protein and then by FACS analysis on at least a tumoral cell line to be sure that the produced antibodies will be able to also recognize the native receptor on tumor cells. This process will be described more precisely in the following examples.
In the same way, the step ii) can also be realized classically by known method or process such as, for example, using 3H-thymidine or any other DNA staining agent, MTT, ATP evaluation, etc. A preferred tumor cell model in the present invention can consist in the BxPC3 model.
By inhibiting c-Met dimerization, it must be understood preferably the c-Met homodimerization.
In a preferred embodiment of the step iii) of selection of the process of the invention, said step iii) consists in evaluating antibodies by BRET analysis on cells expressing both c-Met-RLuc/c-Met-YFP and selecting antibodies capable to inhibit at least 30 %, preferably 35 %, 40 %, 45 %, 50 %, 55 % and most preferably 60 % of the

BRET signal.
The technology BRET is a technology known as being representative of the protein dimerization [Angers et al, PNAS, 2000, 97:3684-89].
The technology BRET, used in the step iii) of the process, is well known by the man skill in the art and will be detailed in the following examples. More particularly, BRET (Bioluminescence Resonance Energy Transfer) is a non-radiative energy transfer occurring between a bio luminescent donor (Renilla Lucif erase (Rluc)) and a fluorescent acceptor, a mutant of GFP (Green Fluorescent Protein) or YFP (Yellow fluorescent protein). In the present case EYFP (Enhanced Yellow Fluorescent Protein) was used. The efficacy of transfer depends on the orientation and the distance between the donor and the acceptor. Then, the energy transfer can occur only if the two molecules are in close proximity (1-10 nm). This property is used to generate protein-protein interaction assays. Indeed, in order to study the interaction between two partners, the first one is genetically fused to the Renilla Luciferase and the second one to the yellow mutant of the GFP. Fusion proteins are generally, but not obligatory, expressed in mammalian cells. In presence of its membrane permeable substrate (coelenterazine), Rluc emits blue light. If the GFP mutant is closer than 10 nm from the Rluc, an energy transfer can occur and an additional yellow signal can be detected. The BRET signal is measured as the ratio between the light emitted by the acceptor and the light emitted by the donor. So the BRET signal will increase as the two fusion proteins are brought into proximity or if a conformational change bring Rluc and GFP mutant closer.
If the BRET analysis consists in a preferred embodiment, any method known by the man skilled in the art can be used to measure c-Met dimerization. Without limitation, the following technologies can be mentioned: FRET (Fluorescence Resonance Energy Transfer), HTRF (Homogenous Time resolved Fluorescence), FLIM (Fluorescence Lifetime Imaging Microscopy) or SW-FCCS single wavelength fluorescence cross-correlation spectroscopy).
Other classical technologies could also be used, such as Co-immunoprecipitation, Alpha screen, Chemical cross-linking, Double-Hybrid, Affinity Chromatography, ELISA or Far western blot.
In a second aspect, a subject of the invention is an isolated antibody, or one of its functional fragments or derivatives, being obtained by said process. Said antibody or one of its said fragments or derivatives, is capable of binding specifically to the human c-Met and, if necessary, preferably moreover capable of inhibiting the natural attachment of its ligand HGF and/or capable of specifically inhibiting the tyrosine kinase activity of said c-Met, said antibody being also capable to inhib c-Met dimerization. More particularly, said antibodies will be capable of inhibiting both ligand-dependent and ligand- independent activation of c-Met.
The expressions "functional fragments and derivatives" will be defined in details later in the present specification.
It must be understood here that the invention does not relate to the antibodies in natural form, that is to say they are not in their natural environment but that they have been able to be isolated or obtained by purification from natural sources, or else obtained by genetic recombination, or by chemical synthesis, and that they can then contain unnatural amino acids as will be described further on.
More particularly, according to another aspect of the invention, it is claimed an antibody, or one of its functional fragments or derivatives, said antibody being characterized in that it comprises at least one complementary determining region CDR chosen from CDRs comprising the amino acid sequence SEQ ID Nos. 1 to 17 and 56 to 61.
Any antibody, or fragments or derivatives, having at least one CDR whose sequence has at least 80 % identity, preferably 85 %, 90 %, 95 % and 98 % identity, after optimum alignment with the sequences SEQ ID Nos. 1 to 17 and 56 to 61 must be understood as a equivalent and, as a consequence, as being part of the invention.
By CDR regions or CDR(s), it is intended to indicate the hypervariable regions of the heavy and light chains of the immunoglobulins as defined by IMGT.
The IMGT unique numbering has been defined to compare the variable domains whatever the antigen receptor, the chain type, or the species [Lefranc M. -P., Immunology Today 18, 509 (1997) / Lefranc M.-P., The Immunologist, 7, 132-136 (1999) / Lefranc, M.-P., Pommie, C, Ruiz, M., Giudicelli, V., Foulquier, E., Truong, L., Thouvenin-Contet, V. and Lefranc, Dev. Comp. Immunol, 27, 55-77 (2003)]. In the IMGT unique numbering, the conserved amino acids always have the same position, for instance cysteine 23 (lst-CYS), tryptophan 41 (CONSERVED-TRP), hydrophobic amino acid 89, cysteine 104 (2nd-CYS), phenylalanine or tryptophan 118 (J-PHE or J-TRP). The IMGT unique numbering provides a standardized delimitation of the framework regions (FRl-IMGT: positions 1 to 26, FR2-IMGT: 39 to 55, FR3-IMGT: 66 to 104 and FR4-IMGT: 118 to 128) and of the complementarity determining regions: CDRl-IMGT: 27 to 38, CDR2-IMGT: 56 to 65 and CDR3-IMGT: 105 to 117. As gaps represent unoccupied positions, the CDR-IMGT lengths (shown between brackets and separated by dots, e.g. [8.8.13]) become crucial information. The IMGT unique numbering is used in 2D graphical representations, designated as IMGT Colliers de Perles [Ruiz, M. and Lefranc, M.-P., Immunogenetics, 53, 857-883 (2002) / Kaas, Q. and Lefranc, M.-P., Current Bioinformatics, 2, 21-30 (2007)], and in 3D structures in IMGT/3Dstructure-DB [Kaas, Q., Ruiz, M. and Lefranc, M.-P., T cell receptor and MHC structural data. Nucl. Acids. Res., 32, D208-D210 (2004)].
Three heavy chain CDRs and 3 light chain CDRs exist. The term CDR or CDRs is used here in order to indicate, according to the case, one of these regions or several, or even the whole, of these regions which contain the majority of the amino acid residues responsible for the binding by affinity of the antibody for the antigen or the epitope which it recognizes.
By "percentage of identity" between two nucleic acid or amino acid sequences in the sense of the present invention, it is intended to indicate a percentage of nucleotides or of identical amino acid residues between the two sequences to be compared, obtained after the best alignment (optimum alignment), this percentage being purely statistical and the differences between the two sequences being distributed randomly and over their entire length. The comparisons of sequences between two nucleic acid or amino acid sequences are traditionally carried out by comparing these sequences after having aligned them in an optimum manner, said comparison being able to be carried out by segment or by "comparison window". The optimum alignment of the sequences for the comparison can be carried out, in addition to manually, by means of the local homology algorithm of Smith and Waterman (1981) [Ad. App. Math. 2:482], by means of the local homology algorithm of Neddleman and Wunsch (1970) [J. MoI. Biol. 48: 443], by means of the similarity search method of Pearson and Lipman (1988) [Proc. Natl. Acad. Sci. USA 85:2444), by means of computer software using these algorithms (GAP, BESTFIT, FASTA and TFASTA in the Wisconsin Genetics Software Package, Genetics Computer Group, 575 Science Dr., Madison, WI, or else by BLAST N or BLAST P comparison software).
The percentage of identity between two nucleic acid or amino acid sequences is determined by comparing these two sequences aligned in an optimum manner and in which the nucleic acid or amino acid sequence to be compared can comprise additions or deletions with respect to the reference sequence for an optimum alignment between these two sequences. The percentage of identity is calculated by determining the number of identical positions for which the nucleotide or the amino acid residue is identical between the two sequences, by dividing this number of identical positions by the total number of positions in the comparison window and by multiplying the result obtained by 100 in order to obtain the percentage of identity between these two sequences.
For example, it is possible to use the BLAST program, "BLAST 2 sequences" (Tatusova et al, "Blast 2 sequences - a new tool for comparing protein and nucleotide sequences", FEMS Microbiol Lett. 174:247-250) available on the site http://www.ncbi.nlm.nih.gov/ gorf/bl2.html, the parameters used being those given by default (in particular for the parameters "open gap penalty": 5, and "extension gap penalty": 2; the matrix chosen being, for example, the matrix "BLOSUM 62" proposed by the program), the percentage of identity between the two sequences to be compared being calculated directly by the program.

By amino acid sequence having at least 80 %, preferably 85 %, 90 %, 95 % and 98 % identity with a reference amino acid sequence, those having, with respect to the reference sequence, certain modifications, in particular a deletion, addition or substitution of at least one amino acid, a truncation or an elongation are preferred. In the case of a substitution of one or more consecutive or nonconsecutive amino acid(s), the substitutions are preferred in which the substituted amino acids are replaced by "equivalent" amino acids. The expression "equivalent amino acids" is aimed here at indicating any amino acid capable of being substituted with one of the amino acids of the base structure without, however, essentially modifying the biological activities of the corresponding antibodies and such as will be defined later, especially in the examples. These equivalent amino acids can be determined either by relying on their structural homology with the amino acids which they replace, or on results of comparative trials of biological activity between the different antibodies capable of being carried out.
By way of example, mention is made of the possibilities of substitution capable of being carried out without resulting in a profound modification of the biological activity of the corresponding modified antibody.
As non limitative example, the following table 1 is giving substitution possibilities conceivable with a conservation of the biological activity of the modified antibody. The reverse substitutions are also, of course, possible in the same conditions.

Table 1

It must be understood here that the invention does not relate to the antibodies in natural form, that is to say they are not in their natural environment but that they have been able to be isolated or obtained by purification from natural sources, or else obtained by genetic recombination, or by chemical synthesis, and that they can then contain unnatural amino acids as will be described further on.
According a first approach, the antibody will be defined by its heavy chain sequence. More particularly, the antibody of the invention, or one of its functional fragments or derivatives, is characterized in that it comprises a heavy chain comprising at least one CDR chosen from CDRs comprising the amino acid sequences SEQ ID

Nos. 1 to 9 and 56 to 58.
The mentioned sequences are the following ones:
SEQ ID No. 1 : GYIFTAYT
SEQ ID No. 2: IKPNNGLA
SEQ ID No. 3 : ARSEITTEFDY SEQ ID No. 4: GYSFTDYT
SEQ ID No. 5 : INPYNGGT
SEQ ID No. 6: AREEITKDFDF
SEQ ID No. 7: GYTFTDYN
SEQ ID No. 8: INPNNGGT
SEQ ID No. 9: ARGRYVGYYYAMDY
SEQ ID No. 56: GYTFTSYW
SEQ ID No. 57: INPTTGST
SEQ ID No. 58: AIGGYGSWF AY

The CDRs of the heavy chain could be chosen randomly in the previous sequences, i.e. SEQ ID Nos. 1 to 9 and 56 to 58.
According to a preferred aspect, the antibody of the invention, or one of its functional fragments or derivatives, comprises a heavy chain comprising at least one CDR chosen from CDR-H 1 , CDR-H2 and CDR-H3 , wherein:
- CDR-Hl comprises the amino acid sequence SEQ ID No. 1, 4, 7 or 56,
- CDR-H2 comprises the amino acid sequence SEQ ID No. 2, 5, 8 or 57, and
- CDR-H3 comprises the amino acid sequence SEQ ID No. 3, 6, 9 or 58.
According to a first embodiment of said aspect, the antibody of the invention, or one of its functional fragments or derivatives, comprises a heavy chain comprising CDR-Hl, CDR-H2 and CDR-H3, wherein CDR-Hl comprises the amino acid sequence SEQ ID No. 1, CDR-H2 comprises the amino acid sequence SEQ ID No. 2 and CDR-H3 comprises the amino acid sequence SEQ ID No. 3.
More particularly, said antibody, or one of its functional fragments or derivatives, according to this first embodiment comprises a heavy chain of sequence comprising the amino acid sequence SEQ ID No. 18.
SEQ ID No. 18: EVQLQQSGPELVKPGASVKISCKTSGYIFTAYTMHWVRQSLG ESLDWIGGIKPNNGLANYNQKFKGKATLTVDKSSSTAYMDLRSLTSEDSAVYY CARSEITTEFDYWGQGTALTVSS

According to a second embodiment of said aspect, the antibody of the invention, or one of its functional fragments or derivatives, comprises a heavy chain comprising CDR-Hl, CDR-H2 and CDR-H3, wherein CDR-Hl comprises the amino acid sequence

SEQ ID No. 4, CDR-H2 comprises the amino acid sequence SEQ ID No. 5 and CDR- H3 comprises the amino acid sequence SEQ ID No. 6.
The antibody, or one of its functional fragments or derivatives, according to said second embodiment will preferably comprise a heavy chain of sequence comprising the amino acid sequence SEQ ID No. 19.
SEQ ID No. 19: EVQLQQSGPELVKPGASMKISCKASGYSFTDYTLNWVKQSH

GKTLEWIGLINPYNGGTTYNQKFKGKATLTVDKSSSTAYMELLSLTSEDSAVY

YCAREEITKDFDFWGQGTTLTVSS

According to a third embodiment of said aspect, the antibody of the invention, or one of its functional fragments or derivatives, comprises a heavy chain comprising

CDR-Hl, CDR-H2 and CDR-H3, wherein CDR-Hl comprises the amino acid sequence

SEQ ID No. 7, CDR-H2 comprises the amino acid sequence SEQ ID No. 8 and CDR-H3 comprises the amino acid sequence SEQ ID No. 9.
The antibody, or one of its functional fragments or derivatives, according to said third embodiment will preferably comprise a heavy chain of sequence comprising the amino acid sequence SEQ ID No. 20.
SEQ ID No. 20: EVLLQQSGPELVKPGASVKIPCKASGYTFTDYNMDWVKQSH GMSLEWIGDINPNNGGTIFNQKFKGKATLTVDKSSSTAYMELRSLTSEDTAVYY

CARGRYVGYYYAMDYWGQGTSVTVSS

According to a fourth embodiment of said aspect, the antibody of the invention, or one of its functional fragments or derivatives, comprises a heavy chain comprising CDR-Hl, CDR-H2 and CDR-H3, wherein CDR-Hl comprises the amino acid sequence

SEQ ID No. 56, CDR-H2 comprises the amino acid sequence SEQ ID No. 57 and CDR-H3 comprises the amino acid sequence SEQ ID No. 58.
The antibody, or one of its functional fragments or derivatives, according to said fourth embodiment will preferably comprise a heavy chain of sequence comprising the amino acid sequence SEQ ID No. 62.
SEQ ID No. 62:
QVQLQQSGAELAKPGASVKMSCKASGYTFTSYWMNWVKQRPGQGLEWIGYI

NPTTGSTDYNQKLKDKATLTADKSSNTAYMQLSSLTSEDSAVYYCAIGGYGSW

FAYWGQGTLVTVSA In a second approach, the antibody will be now define by its light chain sequence. More particularly, according to a second particular aspect of the invention, the antibody, or one of its functional fragments or derivatives, is characterized in that it comprises a light chain comprising at least one CDR chosen from CDRs comprising the amino acid sequence SEQ ID Nos. 10 to 17 and 59 to 61.

The mentioned sequences are the following ones:
SEQ ID No. 10: ESVDSYANSF
SEQ ID No. 11 : RAS
SEQ ID No. 12: QQSKEDPLT
SEQ ID No. 13: ESIDTYGNSF
SEQ ID No. 14: QQSNEDPFT
SEQ ID No. 15: ENIYSN
SEQ ID No. 16: AAT
SEQ ID No. 17: QHFWGPPYT
SEQ ID No. 59: SSVSSTY
SEQ ID No. 60: TTS
SEQ ID No. 61 : HQWSSYPFT

The CDRs of the light chain could be chosen randomly in the previous sequences, i.e. SEQ ID Nos. 10 to 17 and 59 to 61.
According to another preferred aspect, the antibody of the invention, or one of its functional fragments or derivatives, comprises a light chain comprising at least one CDR chosen from CDR-Ll, CDR-L2 and CDR-L3, wherein:
- CDR-Ll comprises the amino acid sequence SEQ ID No. 10, 13, 15 or 59,
- CDR-L2 comprises the amino acid sequence SEQ ID No. 11, 16 or 60, and
- CDR-L3 comprises the amino acid sequence SEQ ID No. 12, 14, 17 or 61.
According to a first embodiment of said another aspect, the antibody of the invention, or one of its functional fragments or derivatives, comprises a light chain comprising CDR-Ll, CDR-L2 and CDR-L3, wherein CDR-Ll comprises the amino acid sequence SEQ ID No. 10, CDR-L2 comprises the amino acid sequence SEQ ID No. 11 and CDR-L3 comprises the amino acid sequence SEQ ID No. 12.

More particularly, said antibody, or one of its functional fragments or derivatives, according to this first embodiment comprises a light chain of sequence comprising the amino acid sequence SEQ ID No. 21.
SEQ ID No. 21 : DIVLTQSPASLAVSLGQRATISCRASESVDSYANSFMHWYQQ KPGQPPKLLIYRASNLESGIPARFSGSGSRTDFTLTINPVEADDVATYYCQQSKE DPLTFGSGTKLEMK

According to a second embodiment of said another aspect, the antibody of the invention, or one of its functional fragments or derivatives, comprises a light chain comprising CDR-Ll, CDR-L2 and CDR-L3, wherein CDR-Ll comprises the amino acid sequence SEQ ID No. 13, CDR-L2 comprises the amino acid sequence SEQ ID No. 11 and CDR-L3 comprises the amino acid sequence SEQ ID No. 14.
The antibody, or one of its functional fragments or derivatives, according to said second embodiment will preferably comprise a light chain of sequence comprising the amino acid sequence SEQ ID No. 22.
SEQ ID No. 22: GIVLTQSPASLAVSLGQRATISCRVSESIDTYGNSFIHWYQQKP GQPPKLLIYRASNLESGIPARFSGSGSRTDFTLTINPVEADDSATYYCQQSNEDPF TFGSGTKLEMK

According to a third embodiment of said another aspect, the antibody of the invention, or one of its functional fragments or derivatives, comprises a light chain comprising CDR-Ll, CDR-L2 and CDR-L3, wherein CDR-Ll comprises the amino acid sequence SEQ ID No. 15, CDR-L2 comprises the amino acid sequence SEQ ID No. 16 and CDR-L3 comprises the amino acid sequence SEQ ID No. 17.
The antibody, or one of its functional fragments or derivatives, according to said third embodiment will preferably comprise a light chain of sequence comprising the amino acid sequence SEQ ID No. 23.
SEQ ID No. 23: DIQMTQSPASLSVSVGETVTITCRASENIYSNLAWYQQKQGKSP

QLLVYAATNLVDGVPSRFSGSGSGTQYSLKINSLQSEDFGSYYCQHFWGPPYTF GGGTKLEIK According to a fourth embodiment of said another aspect, the antibody of the invention, or one of its functional fragments or derivatives, comprises a light chain comprising CDR-Ll, CDR-L2 and CDR-L3, wherein CDR-Ll comprises the amino acid sequence SEQ ID No. 59, CDR-L2 comprises the amino acid sequence SEQ ID No. 60 and CDR-L3 comprises the amino acid sequence SEQ ID No. 61.
The antibody, or one of its functional fragments or derivatives, according to said third embodiment will preferably comprise a light chain of sequence comprising the amino acid sequence SEQ ID No. 63.
SEQ ID No. 63:
QIVLTQSPAIMSASPGEKVTLTCSASSSVSSTYLYWYQQKPGSSPKLWIYTTSIL ASGVPARFSGSGSGTSYSLTISSMETEDAASYFCHQWSSYPFTFGSGTKLDIK

According a third approach, the antibody will be now defined both by its light chain sequence and its heavy chain sequence. The antibody of the invention, or one of its functional fragments or derivatives, is characterized in that it comprises a heavy chain comprising the amino acid sequence SEQ ID No. 18, 19, 20 or 62 and a light chain comprising the amino acid sequence SEQ ID No. 21, 22, 23 or 63.
More particularly, a preferred antibody, or one of its functional fragments or derivatives, according to the invention, named 224Gl 1, comprises a heavy chain comprising CDR-Hl, CDR-H2 and CDR-H3 comprising respectively the amino acid sequence SEQ ID Nos. 1, 2 and 3; and a light chain comprising CDR-Ll, CDR-L2 and

CDR-L3 comprising respectively the amino acid sequence SEQ ID Nos. 10, 11 and 12.

In another aspect, the antibody 224Gl 1 comprises a heavy chain comprising the amino acid sequence SEQ ID No. 18 and a light chain comprising the amino acid sequence SEQ ID No. 21.
Another preferred antibody, or one of its functional fragments or derivatives, according to the invention, named 227Hl, comprises a heavy chain comprising CDR-Hl, CDR-H2 and CDR-H3 comprising respectively the amino acid sequence SEQ ID Nos. 4, 5 and 6; and a light chain comprising CDR-Ll, CDR-L2 and CDR-L3 comprising respectively the amino acid sequence SEQ ID Nos. 13, 11 and 14.

In another aspect, the antibody 227Hl comprises a heavy chain comprising the amino acid sequence SEQ ID No. 19 and a light chain comprising the amino acid sequence SEQ ID No. 22.
Still another preferred antibody, or one of its functional fragments or derivatives, named 223C4, comprises a heavy chain comprising CDR-Hl, CDR-H2 and CDR-H3 comprising respectively the amino acid sequence SEQ ID Nos. 7, 8 and 9; and a light chain comprising CDR-Ll, CDR-L2 and CDR-L3 comprising respectively the amino acid sequence SEQ ID Nos. 15, 16 and 17.
In another aspect, the antibody 223 C4 comprises a heavy chain comprising the amino acid sequence SEQ ID No. 20 and a light chain comprising the amino acid sequence SEQ ID No. 23.
Still another preferred antibody, or one of its functional fragments or derivatives, named HEl, comprises a heavy chain comprising CDR-Hl, CDR-H2 and CDR-H3 comprising respectively the amino acid sequence SEQ ID Nos. 56, 57 and 58; and a light chain comprising CDR-Ll, CDR-L2 and CDR-L3 comprising respectively the amino acid sequence SEQ ID Nos. 59, 60 and 61.
In another aspect, the antibody HEl comprises a heavy chain comprising the amino acid sequence SEQ ID No. 62 and a light chain comprising the amino acid sequence SEQ ID No. 63.
According to another aspect, the invention relates to murine hybridoma capable of secreting monoclonal antibodies according to the present invention, especially hybridoma of murine origin such as deposited at the Collection Nationale de Cultures de Microorganismes (CNCM, National Collection of Microorganism Cultures) (Institut Pasteur, Paris, France).
The monoclonal antibodies according to the invention, or one of their functional fragments or derivatives, are characterized in that said antibodies are secreted by the hybridoma deposited at the CNCM on 03/14/2007 under the numbers CNCM 1-3724 (corresponding to HEl), 1-3731 (corresponding to 224Gl 1), 1-3732 (corresponding to 227H1) and on 07/06/2007 under the number 1-3786 (corresponding to 223C4). These hybridoma consist in murine hybridoma resulting in the cellular fusion of immunized mouse splenocytes with a myeloma cell line (Sp20 Agl4).
The following table 2 regroups elements concerning the preferred antibodies.

Table 2

224Gl 1 227Hl 223C4 HEl
1-3731 1-3732 1-3786 1-3724
Prot. Nucl. Prot ; Nucl. Prot Nucl. Prot. Nucl.
SEQ ID SEQ ID SEQ ] [D SEQ ID SEQ ] [D SEQ ID SEQ ID SEQ ID

CDR-Hl 1 24 4 27 7 30 56 64 CDR-H2 2 25 5 28 8 31 57 65 CDR-H3 3 26 6 29 9 32 58 66

H. chain 18 41 19 42 20 43 62 70

CDR-Ll 10 33 13 36 15 38 59 67 CDR-L2 11 34 11 34 16 39 60 68 CDR-L3 12 35 14 37 17 40 61 69

L. chain 21 44 22 45 23 46 63 71

From table 2, it clearly appears that CDR-L2 of the antibodies 227Hl and 224Gl 1 is similar. This example clearly supports the claims of the present application covering antibodies comprising at least one CDR randomly chosen through described CDR sequences.
According to a preferred embodiment, the invention relates to monoclonal antibodies.
The term « Monoclonal Antibody » or is used in accordance with its ordinary meaning to denote an antibody obtained from a population of substantially homogeneous antibodies, i.e. the individual antibodies comprising the population are identical except for possible naturally occurring mutations that may be present in minor amounts. In other words, a monoclonal antibody consists in a homogenous antibody resulting from the proliferation of a single clone of cells (e.g., hybridoma cells, eukaryotic host cells transfected with DNA encoding the homogenous antibody, prokaryotic host cells transformed with DNA encoding the homogenous antibody, etc.), and which is generally characterized by heavy chains of a single class and subclass, and light chains of a single type. Monoclonal antibodies are highly specific, being directed against a single antigen. Furthermore, in contrast to polyclonal antibodies preparations that typically include different antibodies directed against different determinants, or epitope, each monoclonal antibody is directed against a single determinant on the antigen.

In the present description, the terms polypeptides, polypeptide sequences, amino acid sequences, peptides and proteins attached to antibody compounds or to their sequence are interchangeable.
According to a likewise particular aspect, the present invention relates to a chimeric antibody, or one of its functional fragments, according to the invention, characterized in that said antibody moreover comprises the light chain and heavy chain constant regions derived from an antibody of a species heterologous to the mouse, especially man, and in a preferred manner in that the light chain and heavy chain constant regions derived from a human antibody are respectively the kappa and gamma-1 , gamma-2 or gamma-4 region.
In the present application, IgGl are preferred to get effector functions, and most preferably ADCC and CDC.
The skilled artisan will recognize that effector functions include, for example, CIq binding; complement dependent cytotoxicity (CDC); Fc receptor binding; antibody-dependent cell-mediated cytotoxicity (ADCC); phagocytosis; and down regulation of cell surface receptors (e.g. B cell receptor; BCR).
The antibodies according to the present invention, are preferably specific monoclonal antibodies, especially of murine, chimeric or humanized origin, which can be obtained according to the standard methods well known to the person skilled in the art.
In general, for the preparation of monoclonal antibodies or their functional fragments or derivatives, especially of murine origin, it is possible to refer to techniques which are described in particular in the manual "Antibodies" (Harlow and Lane, Antibodies: A Laboratory Manual, Cold Spring Harbor Laboratory, Cold Spring Harbor NY, pp. 726, 1988) or to the technique of preparation from hybridomas described by

Kohler and Milstein (Nature, 256:495-497, 1975).
The monoclonal antibodies according to the invention can be obtained, for example, from an animal cell immunized against the c-Met, or one of its fragments containing the epitope specifically recognized by said monoclonal antibodies according to the invention. Said c-Met, or one of its said fragments, can especially be produced according to the usual working methods, by genetic recombination starting with a nucleic acid sequence contained in the cDNA sequence coding for the c-Met or by peptide synthesis starting from a sequence of amino acids comprised in the peptide sequence of the c-Met.
The monoclonal antibodies according to the invention can, for example, be purified on an affinity column on which the c-Met or one of its fragments containing the epitope specifically recognized by said monoclonal antibodies according to the invention has previously been immobilized. More particularly, said monoclonal antibodies can be purified by chromatography on protein A and/or G, followed or not followed by ion-exchange chromatography aimed at eliminating the residual protein contaminants as well as the DNA and the LPS, in itself followed or not followed by exclusion chromatography on Sepharose™ gel in order to eliminate the potential aggregates due to the presence of dimers or of other multimers. In an even more preferred manner, the whole of these techniques can be used simultaneously or successively.
Chimeric or humanized antibodies are likewise included in antibodies according to the present invention.
By chimeric antibody, it is intended to indicate an antibody which contains a natural variable (light chain and heavy chain) region derived from an antibody of a given species in combination with the light chain and heavy chain constant regions of an antibody of a species heterologous to said given species (e.g. mouse, horse, rabbit, dog, cow, chicken, etc.).
The antibodies or their fragments of chimeric type according to the invention can be prepared by using the techniques of genetic recombination. For example, the chimeric antibody can be produced by cloning a recombinant DNA containing a promoter and a sequence coding for the variable region of a non-human, especially murine, monoclonal antibody according to the invention and a sequence coding for the constant region of human antibody. A chimeric antibody of the invention encoded by such a recombinant gene will be, for example, a mouse-man chimera, the specificity of this antibody being determined by the variable region derived from the murine DNA and its isotype determined by the constant region derived from the human DNA. For the methods of preparation of chimeric antibodies, it is possible, for example, to refer to the documents Verhoeyn et al. (BioEssays, 8:74, 1988), Morrison et al. (Proc. Natl. Acad. Sci. USA 82:6851-6855, 1984) ou Ie brevet US 4,816,567.

By humanized antibody, it is intended to indicate an antibody which contains CDR regions derived from an antibody of nonhuman origin, the other parts of the antibody molecule being derived from one (or from several) human antibodies. Moreover, some of the residues of the segments of the skeleton (called FR) can be modified in order to conserve the affinity of the binding (Jones et al., Nature, 321 :522-525, 1986; Verhoeyen et al., Science, 239:1534-1536, 1988; Riechmann et al., Nature, 332:323-327, 1988).
The humanized antibodies according to the invention or their fragments can be prepared by techniques known to the person skilled in the art (such as, for example, those described in the documents Singer et al., J. Immun. 150:2844-2857, 1992;

Mountain et al., Biotechnol. Genet. Eng. Rev., 10: 1-142, 1992; or Bebbington et al.,

Bio/Technology, 10:169-175, 1992).
Other humanization method are known by the man skill in the art as, for example, the "CDR Grafting" method described by Protein Design Lab (PDL) in the patent applications EP 0 451261, EP 0 682 040, EP 0 9127, EP 0 566 647 or US 5,530,101, US 6,180,370, US 5,585,089 and US 5,693,761. The following patent applications can also be mentioned: US 5,639,641; US 6,054,297; US 5,886,152 and US 5,877,293.
By "functional fragment" of an antibody according to the invention, it is intended to indicate in particular an antibody fragment, such as Fv, scFv (sc for single chain), Fab, F(ab')2, Fab', scFv-Fc fragments or diabodies, or any fragment of which the half-life time would have been increased by chemical modification, such as the addition of poly(alkylene) glycol such as poly(ethylene) glycol ("PEGylation") (pegylated fragments called Fv-PEG, scFv-PEG, Fab-PEG, F(ab')2-PEG or Fab'-PEG) ("PEG" for Poly(Ethylene) Glycol), or by incorporation in a liposome, said fragments having at least one of the characteristic CDRs of sequence SEQ ID Nos. 1 to 17 and 56 to 61 according to the invention, and, especially, in that it is capable of exerting in a general manner an even partial activity of the antibody from which it is descended, such as in particular the capacity to recognize and to bind to the c-Met, and, if necessary, to inhibit the activity of the c-Met.
Preferably, said functional fragments will be constituted or will comprise a partial sequence of the heavy or light variable chain of the antibody from which they are derived, said partial sequence being sufficient to retain the same specificity of binding as the antibody from which it is descended and a sufficient affinity, preferably at least equal to 1/100, in a more preferred manner to at least 1/10, of that of the antibody from which it is descended, with respect to the c-Met. Such a functional fragment will contain at the minimum 5 amino acids, preferably 6, 7, 8, 9, 10, 12, 15, 25, 50 and 100 consecutive amino acids of the sequence of the antibody from which it is descended.
Preferably, these functional fragments will be fragments of Fv, scFv, Fab, F(ab')2, F(ab'), scFv-Fc type or diabodies, which generally have the same specificity of binding as the antibody from which they are descended. In a more preferred embodiment of the invention, these fragments are selected among divalent fragments such as F(ab')2 fragments. According to the present invention, antibody fragments of the invention can be obtained starting from antibodies such as described above by methods such as digestion by enzymes, such as pepsin or papain and/or by cleavage of the disulfide bridges by chemical reduction. In another manner, the antibody fragments comprised in the present invention can be obtained by techniques of genetic recombination likewise well known to the person skilled in the art or else by peptide synthesis by means of, for example, automatic peptide synthesizers such as those supplied by the company Applied Biosystems, etc.
By "divalent fragment", it must be understood any antibody fragments comprising two arms and, more particularly, F(ab')2 fragments.
More particularly, the invention comprises the antibodies, or their functional fragments, according to the present invention, especially chimeric or humanized antibodies, obtained by genetic recombination or by chemical synthesis.
By « derivatives » of an antibody according to the invention, it is meant a binding protein comprising a protein scaffold and at least on of the CDRs selected from the original antibody in order to maintain the binding capacity. Such compounds are well known by the man skilled in the art and will be described in more details in the following specification.
More particularly, the antibody, or one of its functional fragments or derivatives, according to the invention is characterized in that sand derivative consists in a binding protein comprising a scaffold on which at least one CDR has been grafted for the conservation of the original antibody paratopic recognizing properties.

One or several sequences through the 6 CDR sequences described in the invention can be presented on a protein scaffold. In this case, the protein scaffold reproduces the protein backbone with appropriate folding of the grafted CDR(s), thus allowing it (or them) to maintain their antigen paratopic recognizing properties.
The man skilled in the art knows how to select the protein scaffold on which at least one CDR selected from the original antibody could be grafted. More particularly, it is known that, to be selected, such scaffold should display several features as follow (Skerra A., J. MoI. Recogn., 13, 2000, 167-187):
- phylogenetically good conservation,
- robust architecture with a well known three-dimensional
molecular organization (such as, for example, crystallography or
NMR),
small size,
no or only low degree of post-translational modifications,
- easy to produce, express and purify.
Such protein scaffold can be, but without limitation, structure selected from the group consisting in fibronectin and preferentially the tenth fibronectin type III domain (FNfnlO), lipocalin, anticalin (Skerra A., J. Biotechnol, 2001, 74(4):257-75), the protein Z derivative from the domain B of staphylococcal protein A, thioredoxin A or any protein with repeated domain such as "ankyrin repeat" (Kohl et al., PNAS, 2003, vol. 100, No. 4, 1700-1705), "armadillo repeat", "leucin-rich repeat" or "tetratricopeptide repeat".
It could also be mentioned scaffold derivative from toxins (such as, for example, scorpion, insect, plant or mollusc toxins) or protein inhibitors of neuronal nitric oxyde synthase (PIN).
As non limitative example of such hybrid constructions, it can be mentioned the insertion of the CDR-Hl (heavy chain) of an anti-CD4 antibody, i.e. the 13B8.2 antibody, into one of the exposed loop of the PIN. The binding properties of the obtained binding protein remain similar to the original antibody (Bes et al., BBRC 343, 2006, 334-344). It can also be mentioned the grafting of the CDR-H3 (heavy chain) of an anti-lyzozyme VHH antibody on a loop of neocarzinostatine (Nicaise et al., 2004).
In the case of the present invention, an interesting CDR to conserve could be, without limitation, the CDR-L2 as it is conserved in two identified antibodies of the invention, i.e. 227Hl and 224Gl 1.
As above mentioned, such protein scaffold can comprise from 1 to 6 CDR(s) from the original antibody. In a preferred embodiment, but without any limitation, the man skilled in the art would select at least a CDR from the heavy chain, said heavy chain being known to be particularly implicated in the antibody specificity. The selection of the CDR(s) of interest will be evident for the man of the art with known method (BES et al, FEBS letters 508, 2001, 67-74).
As an evidence, these examples are not limitative and any other scaffold known or described must be included in the present specification.
According to a novel aspect, the present invention relates to an isolated nucleic acid, characterized in that it is chosen from the following nucleic acids:
a) a nucleic acid, DNA or RNA, coding for an antibody, or one of its functional fragments or derivatives, according to the invention;
b) a nucleic acid comprising a DNA sequence selecting from the group of sequences consisting of:
- a nucleic sequence comprising the sequences SEQ ID No. 24, SEQ ID No. 25, SEQ ID No. 26 and the sequences SEQ ID No. 33, SEQ ID No. 34 and SEQ ID No. 35;

- a nucleic sequence comprising the sequences SEQ ID No. 27, SEQ ID No. 28, SEQ ID No. 29 and the sequences SEQ ID No. 36, SEQ ID No. 34 and SEQ ID No. 37;

- a nucleic sequence comprising the sequences SEQ ID No. 30, SEQ ID No. 31, SEQ ID No. 32 and the sequences SEQ ID No. 38, SEQ ID No. 39 and SEQ ID No. 40; and
- a nucleic sequence comprising the sequences SEQ ID No. 64, SEQ ID No. 65, SEQ ID No. 66 and the sequences SEQ ID No. 67, SEQ ID No. 68 and SEQ ID No. 69; c) a nucleic acid comprising a DNA sequence selecting from the group of sequences consisting of:
- a nucleic sequence comprising the sequences SEQ ID No. 41 and SEQ ID No. 44;
- a nucleic sequence comprising the sequences SEQ ID No. 42 and SEQ ID No.

45;

- a nucleic sequence comprising the sequences SEQ ID No. 43 and SEQ ID No. 46, and
- a nucleic sequence comprising the sequences SEQ ID No. 70 and SEQ ID No.

71;
d) the corresponding RNA nucleic acids of the nucleic acids as defined in b) or c);
e) the complementary nucleic acids of the nucleic acids as defined in a), b) and c); and
f) a nucleic acid of at least 18 nucleotides capable of hybridizing under conditions of hight stringency with at least one of the CDRs of sequence SEQ ID Nos.

24 to 40 and 64 to 69.
By nucleic acid, nucleic or nucleic acid sequence, polynucleotide, oligonucleotide, polynucleotide sequence, nucleotide sequence, terms which will be employed indifferently in the present invention, it is intended to indicate a precise linkage of nucleotides, which are modified or unmodified, allowing a fragment or a region of a nucleic acid to be defined, containing or not containing unnatural nucleotides, and being able to correspond just as well to a double-stranded DNA, a single- stranded DNA as to the transcription products of said DNAs.
It must also be understood here that the present invention does not concern the nucleotide sequences in their natural chromosomal environment, that is to say in the natural state. It concerns sequences which have been isolated and/or purified, that is to say that they have been selected directly or indirectly, for example by copy, their environment having been at least partially modified. It is thus likewise intended to indicate here the isolated nucleic acids obtained by genetic recombination by means, for example, of host cells or obtained by chemical synthesis.
An hybridization under conditions of high stringency signifies that the temperature conditions and ionic strength conditions are chosen in such a way that they allow the maintenance of the hybridization between two fragments of complementary DNA. By way of illustration, conditions of high stringency of the hybridization step for the purposes of defining the polynucleotide fragments described above are advantageously the following.

The DNA-DNA or DNA-RNA hybridization is carried out in two steps: (1) prehybridization at 42°C for 3 hours in phosphate buffer (20 mM, pH 7.5) containing 5 x SSC (1 x SSC corresponds to a 0.15 M NaCl + 0.015 M sodium citrate solution), 50 % of formamide, 7 % of sodium dodecyl sulfate (SDS), 10 x Denhardt's, 5 % of dextran sulfate and 1 % of salmon sperm DNA; (2) actual hybridization for 20 hours at a temperature dependent on the size of the probe (i.e.: 42°C, for a probe size > 100 nucleotides) followed by 2 washes of 20 minutes at 200C in 2 x SSC + 2% of SDS, 1 wash of 20 minutes at 200C in 0.1 x SSC + 0.1 % of SDS. The last wash is carried out in 0.1 x SSC + 0.1 % of SDS for 30 minutes at 600C for a probe size > 100 nucleotides. The hybridization conditions of high stringency described above for a polynucleotide of defined size can be adapted by the person skilled in the art for oligonucleotides of greater or smaller size, according to the teaching of Sambrook et al. (1989, Molecular cloning: a laboratory manual. 2nd Ed. Cold Spring Harbor).
The invention likewise relates to a vector comprising a nucleic acid according to the present invention.
The invention aims especially at cloning and/or expression vectors which contain a nucleotide sequence according to the invention.
The vectors according to the invention preferably contain elements which allow the expression and/or the secretion of the nucleotide sequences in a determined host cell. The vector must therefore contain a promoter, signals of initiation and termination of translation, as well as appropriate regions of regulation of transcription. It must be able to be maintained in a stable manner in the host cell and can optionally have particular signals which specify the secretion of the translated protein. These different elements are chosen and optimized by the person skilled in the art as a function of the host cell used. To this effect, the nucleotide sequences according to the invention can be inserted into autonomous replication vectors in the chosen host, or be integrative vectors of the chosen host.
Such vectors are prepared by methods currently used by the person skilled in the art, and the resulting clones can be introduced into an appropriate host by standard methods, such as lipofection, electroporation, thermal shock, or chemical methods.

The vectors according to the invention are, for example, vectors of plasmidic or viral origin. They are useful for transforming host cells in order to clone or to express the nucleotide sequences according to the invention.
The invention likewise comprises the host cells transformed by or comprising a vector according to the invention.
The host cell can be chosen from prokaryotic or eukaryotic systems, for example bacterial cells but likewise yeast cells or animal cells, in particular mammalian cells. It is likewise possible to use insect cells or plant cells.
The invention likewise concerns animals, except man, which comprise at least one cell transformed according to the invention.
According to another aspect, a subject of the invention is a process for production of an antibody, or one of its functional fragments according to the invention, characterized in that it comprises the following stages:
a) culture in a medium and appropriate culture conditions of a host cell according to the invention; and
b) the recovery of said antibodies, or one of their functional fragments, thus produced starting from the culture medium or said cultured cells.
The cells transformed according to the invention can be used in processes for preparation of recombinant polypeptides according to the invention. The processes for preparation of a polypeptide according to the invention in recombinant form, characterized in that they employ a vector and/or a cell transformed by a vector according to the invention, are themselves comprised in the present invention. Preferably, a cell transformed by a vector according to the invention is cultured under conditions which allow the expression of said polypeptide and said recombinant peptide is recovered.
As has been said, the host cell can be chosen from prokaryotic or eukaryotic systems. In particular, it is possible to identify nucleotide sequences according to the invention, facilitating secretion in such a prokaryotic or eukaryotic system. A vector according to the invention carrying such a sequence can therefore advantageously be used for the production of recombinant proteins, intended to be secreted. In effect, the purification of these recombinant proteins of interest will be facilitated by the fact that they are present in the supernatant of the cell culture rather than in the interior of the host cells.
It is likewise possible to prepare the polypeptides according to the invention by chemical synthesis. Such a preparation process is likewise a subject of the invention. The person skilled in the art knows the processes of chemical synthesis, for example the techniques employing solid phases [Steward et al, 1984, Solid phase peptide synthesis,

Pierce Chem. Company, Rockford, 111, 2nd ed., (1984)] or techniques using partial solid phases, by condensation of fragments or by a classical synthesis in solution. The polypeptides obtained by chemical synthesis and being able to contain corresponding unnatural amino acids are likewise comprised in the invention.
The antibodies, or one of their functional fragments or derivatives, capable of being obtained by a process according to the invention are likewise comprised in the present invention.
The invention also concerns the antibody of the invention as a medicament.
The invention likewise concerns a pharmaceutical composition comprising by way of active principle a compound consisting of an antibody, or one of its functional fragments according to the invention, preferably mixed with an excipient and/or a pharmaceutically acceptable vehicle.
Another complementary embodiment of the invention consists in a composition such as described above which comprises, moreover, as a combination product for simultaneous, separate or sequential use, an anti-tumoral antibody.
Most preferably, said second anti-tumoral antibody could be chosen through anti-IGF-IR, anti-EGFR, anti-HER2/neu, anti- VEGFR, anti-VEGF, etc., antibodies or any other anti-tumoral antibodies known by the man skilled in the art. It is evident that the use, as second antibody, of functional fragments or derivatives of above mentioned antibodies is part of the invention.
As a most preferred antibody, anti-EGFR antibodies are selected such as for example the antibody C225 (Erbitux).
"Simultaneous use" is understood as meaning the administration of the two compounds of the composition according to the invention in a single and identical pharmaceutical form.
"Separate use" is understood as meaning the administration, at the same time, of the two compounds of the composition according to the invention in distinct pharmaceutical forms.
"Sequential use" is understood as meaning the successive administration of the two compounds of the composition according to the invention, each in a distinct pharmaceutical form.
In a general fashion, the composition according to the invention considerably increases the efficacy of the treatment of cancer. In other words, the therapeutic effect of the anti-c-Met antibodies according to the invention is potentiated in an unexpected manner by the administration of a cytotoxic agent. Another major subsequent advantage produced by a composition according to the invention concerns the possibility of using lower efficacious doses of active principle, which allows the risks of appearance of secondary effects to be avoided or to be reduced, in particular the effects of the cytotoxic agent.
In addition, this composition according to the invention would allow the expected therapeutic effect to be attained more rapidly.
The composition of the invention can also be characterized in that it comprises, moreover, as a combination product for simultaneous, separate or sequential use, a cytotoxic/cytostatic agent.
By "anti-cancer therapeutic agents" or "cytotoxic/cytostatic agents", it is intended a substance which, when administered to a subject, treats or prevents the development of cancer in the subject's body. As non limitative example of such agents, it can be mentioned alkylating agents, anti-metabolites, anti-tumor antibiotics, mitotic inhibitors, chromatin function inhibitors, anti-angiogenesis agents, anti-estrogens, anti-androgens or immunomodulators.
Such agents are, for example, cited in the 2001 edition of VIDAL, on the page devoted to the compounds attached to the cancerology and hematology column "Cytotoxics", these cytotoxic compounds cited with reference to this document are cited here as preferred cytotoxic agents.
More particularly, the following agents are preferred according to the invention. "Alkylating agent" refers to any substance which can cross-link or alkylate any molecule, preferably nucleic acid (e.g., DNA), within a cell. Examples of alkylating agents include nitrogen mustard such as mechlorethamine, chlorambucol, melphalen, chlorydrate, pipobromen, prednimustin, disodic-phosphate or estramustine; oxazophorins such as cyclophosphamide, altretamine, trofosfamide, sulfofosfamide or ifosfamide; aziridines or imine-ethylenes such as thiotepa, triethylenamine or altetramine; nitrosourea such as carmustine, streptozocin, fotemustin or lomustine; alkyle-sulfonates such as busulfan, treosulfan or improsulfan; triazenes such as dacarbazine; or platinum complexes such as cis-platinum, oxaliplatin and carboplatin.
"Anti-metabolites" refer to substances that block cell growth and/or metabolism by interfering with certain activities, usually DNA synthesis. Examples of antimetabolites include methotrexate, 5-fluoruracil, floxuridine, 5-fluorodeoxyuridine, capecitabine, cytarabine, fludarabine, cytosine arabinoside, 6-mercaptopurine (6-MP), 6-thioguanine (6-TG), chlorodesoxyadenosine, 5-azacytidine, gemcitabine, cladribine, deoxycoformycin and pentostatin.
"Anti-tumor antibiotics" refer to compounds which may prevent or inhibit DNA, RNA and/or protein synthesis. Examples of anti-tumor antibiotics include doxorubicin, daunorubicin, idarubicin, valrubicin, mitoxantrone, dactinomycin, mithramycin, plicamycin, mitomycin C, bleomycin, and procarbazine.
"Mitotic inhibitors" prevent normal progression of the cell cycle and mitosis. In general, microtubule inhibitors or taxoides such as paclitaxel and docetaxel are capable of inhibiting mitosis. Vinca alkaloid such as vinblastine, vincristine, vindesine and vinorelbine are also capable of inhibiting mitosis.
"Chromatin function inhibitors" or "topoisomerase inhibitors" refer to substances which inhibit the normal function of chromatin modeling proteins such as topoisomerase I or topoisomerase II. Examples of chromatin function inhibitors include, for topoisomerase I, camptothecine and its derivatives such as topotecan or irinotecan, and, for topoisomerase II, etoposide, etoposide phosphate and teniposide.
"Anti-angiogenesis agent" refers to any drug, compound, substance or agent which inhibits growth of blood vessels. Exemplary anti-angiogenesis agents include, but are by no means limited to, razoxin, marimastat, batimastat, prinomastat, tanomastat, ilomastat, CGS-27023A, halofuginon, COL-3, neovastat, BMS-275291, thalidomide, CDC 501, DMXAA, L-651582, squalamine, endostatin, SU5416, SU6668, interferon-alpha,EMD121974, interleukin-12, IM862, angiostatin and vitaxin.
"Anti-estrogen" or "anti-estrogenic agent" refer to any substance which reduces, antagonizes or inhibits the action of estrogen. Examples of anti-estrogen agents are tamoxifen, toremifene, raloxifene, droloxifene, iodoxyfene, anastrozole, letrozole, and exemestane.
"Anti-androgens" or "anti-androgen agents" refer to any substance which reduces, antagonizes or inhibits the action of an androgen. Examples of anti-androgens are flutamide, nilutamide, bicalutamide, sprironolactone, cyproterone acetate, finasteride and cimitidine.
"Immunomodulators" are substances which stimulate the immune system.
Examples ofimmunomodulators include interferon, interleukin such as aldesleukine, OCT-43, denileukin diflitox and inter leukin-2, tumoral necrose fators such as tasonermine or others immunomodulators such as lentinan, sizofiran, roquinimex, pidotimod, pegademase, thymopentine, poly I:C or levamisole in conjunction with 5-fluorouracil.
For more detail, the man skill in the art could refer to the manual edited by the "Association Francaise des Enseignants de Chimie Therapeutique" and entitled "traite de chimie therapeutique, vol. 6, Medicaments antitumoraux et perspectives dans Ie traitement des cancers, edition TEC & DOC, 2003".
Can also be mentioned as chemical agents or cytotoxic agents, all kinase inhibitors such as, for example, gefϊtinib or erlotinib.
In a particularly preferred embodiment, said composition as a combination product according to the invention is characterized in that said cytotoxic agent is coupled chemically to said antibody for simultaneous use.
In order to facilitate the coupling between said cytotoxic agent and said antibody according to the invention, it is especially possible to introduce spacer molecules between the two compounds to be coupled, such as poly(alkylene) glycols like polyethylene glycol, or else amino acids, or, in another embodiment, to use active derivatives of said cytotoxic agents into which would have been introduced functions capable of reacting with said antibody according to the invention. These coupling techniques are well known to the person skilled in the art and will not be expanded upon in the present description.

The invention relates, in another aspect, to a composition characterized in that one, at least, of said antibodies, or one of their functional fragments or derivatives, is conjugated with a cell toxin and/or a radioelement.
Preferably, said toxin or said radioelement is capable of inhibiting at least one cell activity of cells expressing the c-Met, in a more preferred manner capable of preventing the growth or the proliferation of said cell, especially of totally inactivating said cell.
Preferably also, said toxin is an enterobacterial toxin, especially Pseudomonas exotoxin A.
The radioelements (or radioisotopes) preferably conjugated to the antibodies employed for the therapy are radioisotopes which emit gamma rays and preferably iodine131, yttrium90, gold199, palladium100, copper67, bismuth217 and antimony211. The radioisotopes which emit beta and alpha rays can likewise be used for the therapy.
By toxin or radioelement conjugated to at least one antibody, or one of its functional fragments, according to the invention, it is intended to indicate any means allowing said toxin or said radioelement to bind to said at least one antibody, especially by covalent coupling between the two compounds, with or without introduction of a linking molecule.
Among the agents allowing binding in a chemical (covalent), electrostatic or noncovalent manner of all or part of the components of the conjugate, mention may particularly be made of benzoquinone, carbodiimide and more particularly EDC (1-ethyl-3-[3-dimethyl-aminopropyl]-carbodiimide hydrochloride), dimaleimide, dithiobis-nitrobenzoic acid (DTNB), N-succinimidyl S-acetyl thio-acetate (SATA), the bridging agents having one or more phenylazide groups reacting with the ultraviolets (U.V.) and preferably N- [-4-(azidosalicylamino)butyl] -3 ' -(2 ' -pyridyldithio)-propionamide (APDP),

N-succinimid-yl 3-(2-pyridyldithio)propionate (SPDP), 6-hydrazino-nicotinamide (HYNIC).
Another form of coupling, especially for the radioelements, can consist in the use of a bifunctional ion chelator.
Among these chelates, it is possible to mention the chelates derived from EDTA

(ethylenediaminetetraacetic acid) or from DTPA (diethylenetriaminepentaacetic acid) which have been developed for binding metals, especially radioactive metals, and immunoglobulins. Thus, DTPA and its derivatives can be substituted by different groups on the carbon chain in order to increase the stability and the rigidity of the ligand-metal complex (Krejcarek et al. (1977); Brechbiel et al. (1991); Gansow (1991); US patent 4,831,175).
For example diethylenetriaminepentaacetic acid (DTPA) and its derivatives, which have been widely used in medicine and in biology for a long time either in their free form, or in the form of a complex with a metallic ion, have the remarkable characteristic of forming stable chelates with metallic ions and of being coupled with proteins of therapeutic or diagnostic interest such as antibodies for the development of radioimmunoconjugates in cancer therapy (Meases et al., (1984); Gansow et al. (1990)).

Likewise preferably, said at least one antibody forming said conjugate according to the invention is chosen from its functional fragments, especially the fragments amputated of their Fc component such as the scFv fragments.
As already mentioned, in a preferred embodiment of the invention, said cytotoxic/cytostatic agent or said toxin and/or a radioelement is coupled chemically to at least one of the elements of said composition for simultaneous use.
The present invention comprises the described composition as a medicament.
The present invention moreover comprises the use of the composition according to the invention for the preparation of a medicament.
In another aspect, the invention deals with the use of an antibody, or one of its functional fragments or derivatives, and/or of a composition as above described for the preparation of a medicament intended to inhibit the growth and/or the proliferation of tumor cells.
Another aspect of the invention consists in the use of an antibody, or one of its functional fragments or derivatives and/or of a composition, as described above or the use above mentioned, for the preparation of a medicament intended for the prevention or for the treatment of cancer.
Is also comprises in the present invention a method intended to inhibit the growth and/or the proliferation of tumor cells in a patient comprising the administration to a patient in need thereof of an antibody, or one of its functional fragments or derivatives according to the invention, an antibody produced by an hybridoma according to the invention or a composition according to the invention.

The present invention further comprises a method for the prevention or the treatment of cancer in a patient in need thereof, comprising the administration to the patient of an antibody, or one of its functional fragments or derivatives according to the invention, an antibody produced by an hybridoma according to the invention or a composition according to the invention.
In a particular preferred aspect, said cancer is a cancer chosen from prostate cancer, osteosarcomas, lung cancer, breast cancer, endometrial cancer, glioblastoma or colon cancer.
As explained before, an advantage of the invention is to allow the treatment of HGF dependent and independent Met-activation related cancers.
The invention, in yet another aspect, encompasses a method of in vitro diagnosis of illnesses induced by an overexpression or an underexpression of the c-Met receptor starting from a biological sample in which the abnormal presence of c-Met receptor is suspected, said method being characterized in that it comprises a step wherein said biological sample is contacted with an antibody of the invention, it being possible for said antibody to be, if necessary, labeled.
Preferably, said illnesses connected with an abnormal presence of c-Met receptor in said diagnosis method will be cancers.
Said antibody, or one of its functional fragments, can be present in the form of an immunoconjugate or of a labeled antibody so as to obtain a detectable and/or quantifiable signal.
The antibodies labeled according to the invention or their functional fragments include, for example, antibodies called immunoconjugates which can be conjugated, for example, with enzymes such as peroxidase, alkaline phosphatase, beta-D-galactosidase, glucose oxydase, glucose amylase, carbonic anhydrase, acetylcholinesterase, lysozyme, malate dehydrogenase or glucose 6-phosphate dehydrogenase or by a molecule such as biotin, digoxygenin or 5-bromodeoxyuridine. Fluorescent labels can be likewise conjugated to the antibodies or to their functional fragments according to the invention and especially include fluorescein and its derivatives, fluorochrome, rhodamine and its derivatives, GFP (GFP for "Green Fluorescent Protein"), dansyl, umbelliferone etc. In such conjugates, the antibodies of the invention or their functional fragments can be prepared by methods known to the person skilled in the art. They can be coupled to the enzymes or to the fluorescent labels directly or by the intermediary of a spacer group or of a linking group such as a polyaldehyde, like glutaraldehyde, ethylenediaminetetraacetic acid (EDTA), diethylene-triaminepentaacetic acid (DPTA), or in the presence of coupling agents such as those mentioned above for the therapeutic conjugates. The conjugates containing labels of fluorescein type can be prepared by reaction with an isothiocyanate.
Other conjugates can likewise include chemo luminescent labels such as luminol and the dioxetanes, bio -luminescent labels such as luciferase and luciferin, or else radioactive labels such as iodine123, iodine125, iodine126, iodine133, bromine77, technetium99"1, indium111, indium113"1, gallium67, gallium68, ruthenium95, ruthenium97, ruthenium103, ruthenium105, mercury107, mercury203, rhenium99"1, rhenium101, rhenium105, scandium47, tellurium121"1, tellurium122"1, tellurium125"1, thulium165, thulium167, thulium168, fluorine18, yttrium199, iodine131. The methods known to the person skilled in the art existing for coupling the therapeutic radioisotopes to the antibodies either directly or via a chelating agent such as EDTA, DTPA mentioned above can be used for the radioelements which can be used in diagnosis. It is likewise possible to mention labeling with Na[I125] by the chloramine T method [Hunter W.M. and Greenwood F. C. (1962) Nature 194:495] or else with technetium99"1 by the technique of Crockford et al. (US patent 4,424,200) or attached via DTPA as described by Hnatowich (US patent 4,479,930).
Thus, the antibodies, or their functional fragments, according to the invention can be employed in a process for the detection and/or the quantification of an overexpression or of an underexpression, preferably an overexpression, of the c-Met receptor in a biological sample, characterized in that it comprises the following steps:
a) the contacting of the biological sample with an antibody, or one of its functional fragments, according to the invention; and
b) the demonstration of the c-Met/antibody complex possibly formed.
In a particular embodiment, the antibodies, or their functional fragments, according to the invention, can be employed in a process for the detection and/or the quantification of the c-Met receptor in a biological sample, for the monitoring of the efficacy of a prophylactic and/or therapeutic treatment of c-Met-dependent cancer.

More generally, the antibodies, or their functional fragments, according to the invention can be advantageously employed in any situation where the expression of the c-Met- receptor must be observed in a qualitative and/or quantitative manner.
Preferably, the biological sample is formed by a biological fluid, such as serum, whole blood, cells, a tissue sample or biopsies of human origin.
Any procedure or conventional test can be employed in order to carry out such a detection and/or dosage. Said test can be a competition or sandwich test, or any test known to the person skilled in the art dependent on the formation of an immune complex of antibody-antigen type. Following the applications according to the invention, the antibody or one of its functional fragments can be immobilized or labeled. This immobilization can be carried out on numerous supports known to the person skilled in the art. These supports can especially include glass, polystyrene, polypropylene, polyethylene, dextran, nylon, or natural or modified cells. These supports can be either soluble or insoluble.
By way of example, a preferred method brings into play immunoenzymatic processes according to the ELISA technique, by immunofluorescence, or radioimmunoassay (RIA) technique or equivalent.
Thus, the present invention likewise comprises the kits or sets necessary for carrying out a method of diagnosis of illnesses induced by an overexpression or an underexpression of the c-Met receptor or for carrying out a process for the detection and/or the quantification of an overexpression or of an underexpression of the c-Met receptor in a biological sample, preferably an overexpression of said receptor, characterized in that said kit or set comprises the following elements:
a) an antibody, or one of its functional fragments, according to the invention; b) optionally, the reagents for the formation of the medium favorable to the immunological reaction;
c) optionally, the reagents allowing the demonstration of c-Met/antibody complexes produced by the immunological reaction.
A subject of the invention is likewise the use of an antibody or a composition according to the invention for the preparation of a medicament intended for the specific targeting of a biologically active compound to cells expressing or overexpressing the c-Met receptor.

It is intended here by biologically active compound to indicate any compound capable of modulating, especially of inhibiting, cell activity, in particular their growth, their proliferation, transcription or gene translation.
A subject of the invention is also an in vivo diagnostic reagent comprising an antibody according to the invention, or one of its functional fragments, preferably labeled, especially radiolabeled, and its use in medical imaging, in particular for the detection of cancer connected with the expression or the overexpression by a cell of the c-Met receptor.
The invention likewise relates to a composition as a combination product or to an anti-c-Met/toxin conjugate or radioelement, according to the invention, as a medicament.
Preferably, said composition as a combination product or said conjugate according to the invention will be mixed with an excipient and/or a pharmaceutically acceptable vehicle.
In the present description, pharmaceutically acceptable vehicle is intended to indicate a compound or a combination of compounds entering into a pharmaceutical composition not provoking secondary reactions and which allows, for example, facilitation of the administration of the active compound(s), an increase in its lifespan and/or in its efficacy in the body, an increase in its solubility in solution or else an improvement in its conservation. These pharmaceutically acceptable vehicles are well known and will be adapted by the person skilled in the art as a function of the nature and of the mode of administration of the active compound(s) chosen.
Preferably, these compounds will be administered by the systemic route, in particular by the intravenous route, by the intramuscular, intradermal, intraperitoneal or subcutaneous route, or by the oral route. In a more preferred manner, the composition comprising the antibodies according to the invention will be administered several times, in a sequential manner.
Their modes of administration, dosages and optimum pharmaceutical forms can be determined according to the criteria generally taken into account in the establishment of a treatment adapted to a patient such as, for example, the age or the body weight of the patient, the seriousness of his/her general condition, the tolerance to the treatment and the secondary effects noted.

Other characteristics and advantages of the invention appear in the continuation of the description with the examples and the figures wherein:
Figure 1 : Examples of FACS profiles of the selected anti-c-Met antibodies;
Figures 2 A and 2B: In vitro inhibition of BXPC3 proliferation by antibodies targeting c-Met;
Figure 3 : Inhibition of c-Met dimerization;
Figure 4: Protein recognition by anti-c-Met antibodies;
Figures 5A and 5B: "Epitope mapping" of 1 IEl and 5D5 by BIAcore analysis;

Figures 6A and 6B: Effect of MAbs on c-Met phosphorylation;
Figures 7A and 7B: Displacement of radio-labeled HGF by anti-c-Met antibodies;
Figure 8: Inhibition of invasion by anti-c-Met antibodies [in this figure, SVF means Fetal Calf Serum (FCS)];
Figure 9: Effect of anti c-Met antibodies on wound healing;
Figures 1OA and 1OB: Scatter assay;
Figure 11 : Three-dimensional tubulogenesis assay;
Figures 12A and 12B: Effect of antibodies on spheroid formation;
Figure 13: In vivo activity of anti-c-Met Mabs in the U87MG xenograft model;

Figure 14: HGF expression by a set of tumour cell lines;
Figures 15A and 15B: Characterization of the NCI-H441 cell line; with figure

15A corresponding to quantitative RT-PCR analysis and figure 15B corresponding to FACS analysis;
Figure 16: In vivo activity of anti-c-Met antibodies on NCI-H441 xenograft model;
Figure 17A: Alignment of 224Gl 1 VL to murine IGKV3-5*01 germline gene;

Figure 17B: Alignment of 224Gl 1 VL to murine IGKJ4*01 germline gene;
Figure 18A: Alignment of 224Gl 1 VL to human IGKV3-l l*01 and IGKV4-1*01 germline genes;
Figure 18B: Alignment of 224Gl 1 VL to human IGKJ4*02 germline gene;
Figure 19A: IGKV3-l l*01 based humanized version of 224Gl 1 VL with mentioned mutations;
Figure 19B: IGKV4-l*01 based humanized version of 224Gl 1 VL with mentioned mutations;
Figure 2OA: Alignment of 224Gl 1 VH to murine IGHV1-18*O1 germline gene; Figure 2OB: Alignment of 224Gl 1 VH to murine IGHD2-4*01 germline gene; Figure 2OC: Alignment of 224Gl 1 VH to murine IGHJ2*01 germline gene;
Figure 21A: Alignment of 224Gl 1 VH to human IGHV1-2*O2 germline gene;

Figure 2 IB: Alignment of 224G11 VH to human IGHJ4*01 germline gene;
Figure 22: Humanized 224Gl 1 VH with mentioned mutations;
Figure 23A: Alignment of 227Hl VL to murine IGKV3-5*01 germline gene;
Figure 23B: Alignment of 227Hl VL to murine IGKJ4*01 germline gene;
Figure 24A: Alignment of 227Hl VL to human IGKV3-11*01 and IGKV4-l*01 germline genes;
Figure 24B: Alignment of 227Hl VL to human IGKJ4*02 germline gene;
Figure 25A: IGKV3-l l*01 based humanized version of 227Hl VL with mentioned mutations;
Figure 25B: IGKV4-l*01 based humanized version of 227Hl VL with mentioned mutations;
Figure 26A: Alignment of 227Hl VH to murine IGHVl-18*01 germline gene; Figure 26B: Alignment of 227Hl VH to murine IGHDl-I* 02 germline gene;
Figure 26C: Alignment of 227Hl VH to murine IGHJ2*01 germline gene;
Figure 27A: Alignment of 227Hl VH to human IGHV1-2*O2 germline gene;
Figure 27B: Alignment of 227Hl VH to human IGHJ4*01 germline gene;
Figure 28: Humanized 227Hl VH with mentioned mutations;
Figure 29A: Alignment of 223C4 VL to murine IGKV12-46*01 germline gene; Figure 29B: Alignment of 223C4 VL to murine IGKJ2*01 germline gene;
Figure 30A: Alignment of 223C4 VL to human IGKVl-NLl *01 germline gene;

Figure 30B: Alignement of 223C4 VL to human IGKJ2*01 germline gene;
Figure 31 : Humanized 223 C4 VL with mentioned mutations;
Figure 32A: Alignment of 223C4 VH to murine IGHVl-18*01 germline gene; Figure 32B: Alignment of 223C4 VH to murine IGHD6-3*01 germline gene;
Figure 32C: Alignment of 223C4 VH to murine IGHJ4*01 germline gene;
Figure 33 A: Alignment of 223C4 VH to human IGHV 1-2* 02 germline gene;
Figure 33B: Alignment of 223C4 VH to human IGHD1-26*O1 germline gene;

Figure 33C: Alignment of 223C4 VH to human IGHJ6*01 germline gene; and
Figure 34: Humanized 223C4 VH with mentioned mutations;
Figure 35: Anti-tumor activity of the murine 224Gl 1 Mab alone or combined with Navelbine® on the established xenograft NCI-H441 tumor model;
Figure 36: Evaluation of anti-c-Met Mabs on HUVEC proliferation;
Figure 37: Evaluation of anti-c-Met Mabs on HUVEC tube formation;
Figure 38A: Alignment of 1 IEl VL to murine IGKV4-79*01 germline gene;
Figure 38B: Alignment of 1 IEl VL to murine IGKJ4*01 germline gene;
Figure 39A: Alignment of 1 IEl VL to human IGKV3D-7*01 germline gene;
Figure 39B: Alignment of 1 IEl VL to human IGKJ4*02 germline gene;
Figure 40: Humanized version of 1 IEl VL with mentioned mutations;
Figure 41A: Alignment of 1 IEl VH to murine IGHV1-7*O1 germline gene;
Figure 4 IB: Alignment of 1 IEl VH to murine IGHD4-l*01 germline gene;
Figure 41C: Alignment of 1 IEl VH to murine IGHJ3*01 germline gene;
Figure 42A: Alignment of 1 IEl VH to human IGHV1-2*O2 and IGHV1-46*O1 germline genes;
Figure 42B: Alignment of 1 IEl VH to human IGHJ4*03 germline gene;
Figure 43: Humanized 1 IEl VH with mentioned mutations;
Figures 44A and 44B: c-Met Phosphorylation assay on A549 cells. Evaluation of HEl and 224Gl 1 purified Mabs, in absence or in presence of HGF, either at 30 μg/ml (figure 44A) or within a dose range from 0.0015 to 30 μg/ml in order to determine EC50 values (figure 44B);
Figure 45: In vivo combination of 224Gl 1 Mab with Navelbine® in the NSCLC NCI-H441 xenograft model;
Figure 46: In vivo combination of 224Gl 1 Mab with Doxorubicin in the NSCLC

NCI-H441 xenograft model;
Figure 47: In vivo combination of 224Gl 1 Mab with Docetaxel in the NSCLC NCI-H441 xenograft model;
Figure 48: In vivo combination of 224Gl 1 Mab with Temozolomide in the NSCLC NCI-H441 xenograft model;
Figures 49A, 49B, 49C and 49D: Effect of anti-c-Met Mabs on U87-MG spheroid growth;

Figures 5OA and 5OB: In vitro activity of chimeric and humanized forms of 224Gl 1 in the phospho-c-Met assay;
Figure 51 : Settings of Biacore analysis;
Figure 52: In vivo activity of 224Gl 1 on MDA-MB-231 cells co-implanted with MRC5 cells as human HGF source on Athymic nude mice;
Figure 53: ELISA based binding assay to Fc-cMet. Anti-Fc-c-Met binding activity was measured in an ELISA-based assay where anti-murine Fc conjugates was used to detect the purified murine monoclonal antibodies HEl, 224Gl 1 and 227Hl.

Dose-dependent binding activities onto plastic-coated recombinant Fc-cMet was measured at 450nm;
Figure 54: HGF-cMet competition assay. In this ELISA-based assay, recombinant Fc-cMET residual binding to plastic coated HGF in the presence of purified murine monoclonal antibodies HEl, 224Gl 1 and 227Hl was detected with anti-murine Fc conjugate and measured at 450 nm;
Figure 55: Amino acid sequences alignment of 227Hl -derived recombinant VH domains. The 227Hl VH amino acid sequence is aligned with the selected human receiving framework sequence, with only mentioned the amino acids that were found different from the murine 227Hl VH sequence. 227Hl HZl, HZ2 and HZ3 VH sequences correspond to implemented humanized versions of the 227Hl murine VH domain, with remaining murine residues in bold. In HZ3, 10 residues (*) were automatically changed for their human counterparts. In HZ2, the seven residues from the third group (3) have been studied. In HZlVH, the nine residues from the second group (2) have been mutated into their human counterparts, only the six residues from the first group (1) remain murine;
Figure 56: ELISA based binding assay to Fc-cMet of recombinant 227Hl antibodies. Anti-Fc-cMet binding activity was measured in an ELISA-based assay where anti- human Fc conjugates was used to detect chimeric and humanized 227Hl -derived recombinant antibodies. Dose-dependent binding activities onto plastic-coated recombinant Fc-cMet of humanized VH domains-derived 227Hl antibodies was measured at 450nm and then compare to those of the parental/reference chimeric antibody;
Figure 57: ELISA based binding assay to Fc-cMet of recombinant 227Hl - derived antibodies. Anti-Fc-cMet binding activity was measured in an ELISA-based assay where anti-human Fc conjugates was used to detect chimeric and humanized 227Hl -derived recombinant antibodies. Dose-dependent binding activity onto plastic-coated recombinant Fc-cMet of humanized HZ4VH-derived 227Hl antibody was measured at 450nm and then compared to those of the parental/reference chimeric antibody;
Figure 58: HGF-cMet competition assay of 227Hl murine and recombinant antibodies. In this ELISA-based assay, recombinant Fc-cMet residual binding to plastic coated HGF in the presence of the different forms of the 227Hl antibody was detected with a biotinylated unrelated anti-cMet antibody. Purified murine 227Hl monoclonal antibody, chimeric and HZ4VH-derived humanized 227Hl -derived recombinant antibodies were tested and compared for their abilities to compete with HGF-cMet binding when measured at 450nm;
Figure 59: 227H1-HZ VH humanized variable domain sequence. *, corresponds to amino acids changed de facto to their human counterparts; !, corresponds to amino acids humanized during the HZ3 to HZl implementation; §, corresponds to amino acids humanized in the final 227Hl -HZ VH sequence;
Figure 60: Amino acid sequences alignment of HEl -derived recombinant VH domains. The HEl VH amino acid sequence is aligned with the selected human receiving framework sequence, with only mentioned the amino acids that were found different from the murine 1 IEl VH sequence. 1 IEl HZ VHl, VH2 and VH3 sequences correspond to implemented humanized versions of the 1 IEl murine VH domain, with remaining murine residues in bold. In HZ VH3, seven residues (*) were automatically changed for their human counterparts. In HZ VH2, the seven residues from the third group (3) have been studied. In HZ VHl, the five residues from the second group (2) have been mutated into their human counterparts, only the five residues from the first group (1) remain murine;
Figure 61: ELISA based binding assay to Fc-cMet of recombinant 1 IEl antibodies. Anti-Fc-cMet binding activity was measured in an ELISA-based assay where anti- human Fc conjugates was used to detect chimeric and humanized 1 IEl-derived recombinant antibodies. Dose-dependent binding activities onto plastic-coated recombinant Fc-cMet of humanized VH domains-derived 1 IEl antibodies was measured at 450nm and then compare to those of the parental/reference chimeric antibody;
Figure 62: Amino acid sequences alignment of HEl -derived recombinant VL domains. The HEl VL amino acid sequence is aligned with the selected human receiving framework sequence, with only mentioned the amino acids that were found different from the murine 1 IEl VL sequence. 1 IEl HZ VLl, VL2 and VL3 sequences correspond to implemented humanized versions of the 1 IEl murine VL domain, with remaining murine residues in bold. In HZ VL3, ten residues (*) were automatically changed for their human counterparts. In HZ VL2, the eight residues from the third group (3) have been studied. In HZ VLl, the eight residues from the second group (2) have been mutated into their human counterparts, only the four residues from the first group (1) remain murine;
Figure 63: ELISA based binding assay to Fc-cMet of recombinant 1 IEl antibodies. Anti-Fc-cMet binding activity was measured in an ELISA-based assay where anti- human Fc conjugates was used to detect chimeric and humanized 1 IEl-derived recombinant antibodies. Dose-dependent binding activities onto plastic-coated recombinant Fc-cMet of humanized VL domains-derived 1 IEl antibodies was measured at 450nm and then compare to those of the parental/reference chimeric antibody;
Figure 64: ELISA based binding assay to Fc-cMet of recombinant 1 IEl antibodies. Anti-Fc-cMet binding activity was measured in an ELISA-based assay where anti- human Fc conjugates was used to detect chimeric and humanized 1 IEl-derived recombinant antibodies. Dose-dependent binding activities onto plastic-coated recombinant Fc-cMet of single or double humanized domains-derived 1 IEl antibodies was measured at 450nm and then compared to those of the parental/reference chimeric antibody;
Figure 65: Amino acid sequences alignment of 224Gl 1 VH domain sequence. The 224Gl 1 VH amino acid sequence is aligned with the 227Hl VH sequence (underlined are non homologous residues) and with the selected human receiving framework sequence, with only mentioned the amino acids that were found different from the murine 224Gl 1 VH sequence. 224Gl 1 HZ VHO sequence correspond to "227Hl-based/full-IMGT" humanized version of the 224Gl 1 murine VH domain. In this sequence no outside-IMGT-CDRs residues remain murine;
Figure 66: ELISA based binding assay to Fc-cMet of recombinant 224Gl 1 antibodies. Anti-Fc-cMet binding activity was measured in an ELISA-based assay where anti-human Fc conjugates was used to detect chimeric and HZVHO-derived humanized 224Gl 1 -derived recombinant antibodies. Dose-dependent binding activity onto plastic-coated recombinant Fc-cMet of the HZVHO "full-IMGT" humanized VH domain-derived 224Gl 1 antibody was measured at 450nm and then compared to those of the parental/reference chimeric antibody;
Figure 67: HGF-cMet competition assay of 224Gl 1 murine and recombinant antibodies. In this ELISA-based assay, recombinant Fc-cMet residual binding to plastic coated HGF in the presence of the different forms of the 224Gl 1 antibody was detected with a biotinylated unrelated anti-cMet antibody. Purified murine 224Gl 1 monoclonal antibody, chimeric and HZVHO-derived humanized 224Gl 1 -derived recombinant antibodies were tested and compared for their abilities to compete with HGF-cMet binding when measured at 450nm;

CLAIMS

1. Process for the selection of an anti c-Met antibody, or one of its functional "divalent fragments" or "derivatives", capable to inhibit both ligand-dependent and ligand- independent activation of c-Met, characterized in that it comprises the following steps:
i) screening the generated antibodies and selecting antibodies capable to bind specifically to c-Met;
ii) evaluating in vitro the selected antibodies of step i) and selecting antibodies capable to inhibit at least 50 % of tumoral cell proliferation for at least one tumor type; and then
iii) testing the selected antibodies of step ii) and selecting antibodies capable to inhibit the c-Met dimerization.
2. Process according to claim 1, wherein step iii) consists in evaluating antibodies by BRET analysis on cells expressing both c-Met-RLuc/c-Met-YFP and selecting antibodies capable to inhibit at least 30 %, of the BRET signal.
3. An isolated antibody, or one of its functional "divalent fragments" or "derivatives", capable of being obtained by a process as claimed in claim 1 or 2.
4. The antibody of claim 3, or one of its functional "divalent fragments" or "derivatives", characterized in that it comprises at least one complementary determining region CDR chosen from CDRs comprising the amino acid sequences SEQ ID Nos. 1 to 17 and 56 to 61.
5. The antibody of claim 3, or one of its functional "divalent fragments" or "derivatives", characterized in that it comprises a heavy chain comprising at least one CDR chosen from CDRs comprising the amino acid sequences SEQ ID Nos. 1 to 9 and

56 to 58.
6. The antibody of claim 5, or one of its functional "divalent fragments" or "derivatives", characterized in that it comprises a heavy chain comprising at least one CDR chosen from CDR-Hl, CDR-H2 and CDR-H3, wherein:
- CDR-Hl comprises the amino acid sequence SEQ ID No. 1, 4, 7 or 56,
- CDR-H2 comprises the amino acid sequence SEQ ID No. 2, 5, 8 or 57, and
- CDR-H3 comprises the amino acid sequence SEQ ID No. 3, 6, 9 or 58.

93

7. The antibody of claim 6, or one of its functional "divalent fragments" or "derivatives", characterized in that it comprises a heavy chain comprising CDR-Hl, CDR-H2 and CDR-H3, wherein CDR-Hl comprises the amino acid sequence SEQ ID No. 1, CDR-H2 comprises the amino acid sequence SEQ ID No. 2 and CDR-H3 comprises the amino acid sequence SEQ ID No. 3.
8. The antibody of claim 7, or one of its functional "divalent fragments" or "derivatives", characterized in that it comprises a heavy chain of sequence comprising the amino acid sequence SEQ ID No. 18.
9. The antibody of claim 6, or one of its functional "divalent fragments" or "derivatives", characterized in that it comprises a heavy chain comprising CDR-Hl,

CDR-H2 and CDR-H3, wherein CDR-Hl comprises the amino acid sequence SEQ ID No. 4, CDR-H2 comprises the amino acid sequence SEQ ID No. 5 and CDR-H3 comprises the amino acid sequence SEQ ID No. 6.
10. The antibody of claim 9, or one of its functional "divalent fragments" or "derivatives", characterized in that it comprises a heavy chain of sequence comprising the amino acid sequence SEQ ID No. 19.
11. The antibody of claim 6, or one of its functional "divalent fragments" or "derivatives", characterized in that it comprises a heavy chain comprising CDR-Hl, CDR-H2 and CDR-H3, wherein CDR-Hl comprises the amino acid sequence SEQ ID No. 7, CDR-H2 comprises the amino acid sequence SEQ ID No. 8 and CDR-H3 comprises the amino acid sequence SEQ ID No. 9.
12. The antibody of claim 11, or one of its functional "divalent fragments" or "derivatives", characterized in that it comprises a heavy chain of sequence comprising the amino acid sequence SEQ ID No. 20.
13. The antibody of claim 6, or one of its functional "divalent fragments" or

"derivatives", characterized in that it comprises a heavy chain comprising CDR-Hl, CDR-H2 and CDR-H3, wherein CDR-Hl comprises the amino acid sequence SEQ ID No. 56, CDR-H2 comprises the amino acid sequence SEQ ID No. 57 and CDR-H3 comprises the amino acid sequence SEQ ID No. 58.
14. The antibody of claim 13, or one of its functional "divalent fragments" or

"derivatives", characterized in that it comprises a heavy chain of sequence comprising the amino acid sequence SEQ ID No. 62.

94

15. The antibody of claim 3, or one of its functional "divalent fragments" or "derivatives", characterized in that it comprises a light chain comprising at least one CDR chosen from CDRs comprising the amino acid sequence SEQ ID Nos. 10 to 17 and 59 to 61.
16. The antibody of claim 15, or one of its functional "divalent fragments" or

"derivatives", characterized in that it comprises a light chain comprising at least one CDR chosen from CDR-Ll, CDR-L2 and CDR-L3, wherein:
- CDR-Ll comprises the amino acid sequence SEQ ID No. 10, 13, 15 or 59,
- CDR-L2 comprises the amino acid sequence SEQ ID No. 11, 16 or 60, and
- CDR-L3 comprises the amino acid sequence SEQ ID No. 12, 14, 17 or 61.
17. The antibody of claim 16, or one of its functional "divalent fragments" or "derivatives", characterized in that it comprises a light chain comprising CDR-Ll, CDR-L2 and CDR-L3, wherein CDR-Ll comprises the amino acid sequence SEQ ID No. 10, CDR-L2 comprises the amino acid sequence SEQ ID No. 11 and CDR-L3 comprises the amino acid sequence SEQ ID No. 12.
18. The antibody of claim 17, or one of its functional "divalent fragments" or "derivatives", characterized in that it comprises a light chain of sequence comprising the amino acid sequence SEQ ID No. 21.
19. The antibody of claim 16, or one of its functional "divalent fragments" or "derivatives", characterized in that it comprises a light chain comprising CDR-Ll,

CDR-L2 and CDR-L3, wherein CDR-Ll comprises the amino acid sequence SEQ ID No. 13, CDR-L2 comprises the amino acid sequence SEQ ID No. 11 and CDR-L3 comprises the amino acid sequence SEQ ID No. 14.
20. The antibody of claim 19, or one of its functional "divalent fragments" or "derivatives", characterized in that it comprises a light chain of sequence comprising the amino acid sequence SEQ ID No. 22.
21. The antibody of claim 16, or one of its functional "divalent fragments" or "derivatives", characterized in that it comprises a light chain comprising CDR-Ll, CDR-L2 and CDR-L3, wherein CDR-Ll comprises the amino acid sequence SEQ ID No. 15, CDR-L2 comprises the amino acid sequence SEQ ID No. 16 and CDR-L3 comprises the amino acid sequence SEQ ID No. 17.
22. The antibody of claim 21, or one of its functional "divalent fragments" or 95

"derivatives", characterized in that it comprises a light chain of sequence comprising the amino acid sequence SEQ ID No. 23.
23. The antibody of claim 16, or one of its functional "divalent fragments" or "derivatives", characterized in that it comprises a light chain comprising CDR-Ll, CDR-L2 and CDR-L3, wherein CDR-Ll comprises the amino acid sequence SEQ ID No. 59, CDR-L2 comprises the amino acid sequence SEQ ID No. 60 and CDR-L3 comprises the amino acid sequence SEQ ID No. 61.
24. The antibody of claim 23, or one of its functional "divalent fragments" or "derivatives", characterized in that it comprises a light chain of sequence comprising the amino acid sequence SEQ ID No. 63.
25. The antibody of claim 3, or one of its functional "divalent fragments" or "derivatives", characterized in that it comprises a heavy chain comprising the amino acid sequence SEQ ID No. 18, 19, 20 or 62 and a light chain comprising the amino acid sequence SEQ ID No. 21, 22, 23 or 63.
26. The antibody of claim 3, or one of its functional "divalent fragments" or

"derivatives", characterized in that it comprises a heavy chain comprising CDR-Hl, CDR-H2 and CDR-H3 comprising respectively the amino acid sequence SEQ ID Nos. 1, 2 and 3; and a light chain comprising CDR-Ll, CDR-L2 and CDR-L3 comprising respectively the amino acid sequence SEQ ID Nos. 10, 11 and 12.
27. The antibody of claim 26, or one of its functional "divalent fragments" or

"derivatives", characterized in that it comprises a heavy chain comprising the amino acid sequence SEQ ID No. 18 and a light chain comprising the amino acid sequence SEQ ID No. 21.
28. A murine hybridoma capable of secreting an antibody as claimed in claim 27.
29. The murine hybridoma as claimed in claim 28 deposited at the CNCM, Institut Pasteur, Paris, on March 14, 2007 under the number 1-3731.
30. The antibody of claim 3, or one of its functional "divalent fragments" or "derivatives", characterized in that it comprises a heavy chain comprising CDR-Hl, CDR-H2 and CDR-H3 comprising respectively the amino acid sequence SEQ ID Nos.

4, 5 and 6; and a light chain comprising CDR-Ll, CDR-L2 and CDR-L3 comprising respectively the amino acid sequence SEQ ID Nos. 13, 11 and 14.

96

31. The antibody of claim 30, or one of its functional "divalent fragments" or "derivatives", characterized in that it comprises a heavy chain comprising the amino acid sequence SEQ ID No. 19 and a light chain comprising the amino acid sequence SEQ ID No. 22.
32. A murine hybridoma capable of secreting an antibody as claimed in claim

31.
33. The murine hybridoma as claimed in claim 32 deposited at the CNCM, Institut Pasteur, Paris, on March 14, 2007 under the number 1-3732.
34. The antibody of claim 3, or one of its functional "divalent fragments" or "derivatives", characterized in that it comprises a heavy chain comprising CDR-Hl,

CDR-H2 and CDR-H3 comprising respectively the amino acid sequence SEQ ID Nos. 7, 8 and 9; and a light chain comprising CDR-Ll, CDR-L2 and CDR-L3 comprising respectively the amino acid sequence SEQ ID Nos. 15, 16 and 17.
35. The antibody of claim 34, or one of its functional "divalent fragments" or "derivatives", characterized in that it comprises a heavy chain comprising the amino acid sequence SEQ ID No. 20 and a light chain comprising the amino acid sequence SEQ ID No. 23.
36. A murine hybridoma capable of secreting an antibody as claimed in claim 35.
37. The murine hybridoma as claimed in claim 36 deposited at the CNCM,

Institut Pasteur, Paris, on July 6, 2007 under the number 1-3786.
38. The antibody of claim 3, or one of its functional "divalent fragments" or "derivatives", characterized in that it comprises a heavy chain comprising CDR-Hl, CDR-H2 and CDR-H3, comprising respectively the amino acid sequence SEQ ID Nos. 56, 57 and 58; and a light chain comprising CDR-Ll, CDR-L2 and CDR-L3 comprising respectively the amino acid sequence SEQ ID Nos. 59, 60 and 61.
39. The antibody of claim 38, or one of its functional "divalent fragments" or "derivatives", characterized in that it comprises a heavy chain comprising the amino acid sequence SEQ ID No. 62 and a light chain comprising the amino acid sequence SEQ ID No. 63.
40. A murine hybridoma capable of secreting an antibody as claimed in claim 39.

97

41. The murine hybridoma as claimed in claim 40 deposited at the CNCM, Institut Pasteur, Paris, on March 14, 2007 under the number 1-3724.
42. The antibody of claims 3-27, 30, 31, 34, 35, 38 or 39, or one of its functional "divalent fragments" or "derivatives", characterized in that it consists in a monoclonal antibody.
43. The antibody of claim 42, or one of its functional "divalent fragments", characterized in that said antibody is a chimeric antibody and moreover comprises the light chain and heavy chain constant regions derived from an antibody of a species heterologous to the mouse.
44. The chimeric antibody of claim 43, or one of its functional "divalent fragments", characterized in that said heterologous species is man.
45. The humanized antibody of claim 44, or one of its functional "divalent fragments" or "derivatives", characterized in that the light chain and heavy chain constant regions derived from a human antibody are respectively for the light chain the kappa region and for the heavy chain the gamma- 1, gamma-2 or gamma-4 region.
46. An isolated nucleic acid, characterized in that it is chosen from the following nucleic acids:
a) a nucleic acid, DNA or RNA, coding for an antibody, or one of its functional "divalent fragments" or "derivatives", as claimed in one of claims 3-27, 30, 31, 34, 35, 38, 39 and 42-45;
b) a nucleic acid comprising a DNA sequence selecting from the group of sequences consisting of:
- a nucleic sequence comprising the sequences SEQ ID No. 24, SEQ ID No. 25, SEQ ID No. 26 and the sequences SEQ ID No. 33, SEQ ID No. 34 and SEQ ID No. 35; - a nucleic sequence comprising the sequences SEQ ID No. 27, SEQ ID No. 28,

SEQ ID No. 29 and the sequences SEQ ID No. 36, SEQ ID No. 34 and SEQ ID No. 37;

- a nucleic sequence comprising the sequences SEQ ID No. 30, SEQ ID No. 31, SEQ ID No. 32 and the sequences SEQ ID No. 38, SEQ ID No. 39 and SEQ ID No. 40, and
- a nucleic sequence comprising the sequences SEQ ID No. 64, SEQ ID No. 65,

SEQ ID No. 66 and the sequences SEQ ID No. 67, SEQ ID No. 68 and SEQ ID No. 69; c) a nucleic acid comprising a DNA sequence selecting from the group of 98

sequences consisting of:
- a nucleic sequence comprising the sequences SEQ ID No. 41 and SEQ ID No. 44;
- a nucleic sequence comprising the sequences SEQ ID No. 42 and SEQ ID No. 45;
- a nucleic sequence comprising the sequences SEQ ID No. 43 and SEQ ID No. 46;
- a nucleic sequence comprising the sequences SEQ ID No. 70 and SEQ ID No.

71;
d) the corresponding RNA nucleic acids of the nucleic acids as defined in b) or c);
e) the complementary nucleic acids of the nucleic acids as defined in a), b) and c); and
f) a nucleic acid of at least 18 nucleotides capable of hybridizing under conditions of hight stringency with at least one of the CDRs of sequence SEQ ID Nos.

24 to 40 and 64 to 69.
47. A vector comprising a nucleic acid as claimed in claim 46.
48. A host cell comprising a vector as claimed in claim 47.
49. A transgenic animal with the exception of man comprising at least one cell transformed by a vector as claimed in claim 47.
50. A process for production of an antibody, or one of its functional "divalent fragments", as claimed in one of claims 3-27, 30, 31, 34, 35, 38, 39 and 42-45, characterized in that it comprises the following stages:
a) culture in a medium and appropriate culture conditions of a cell as claimed in claim 48; and
b) the recovery of said antibodies, or one of their functional "divalent fragments", thus produced starting from the culture medium or said cultured cells.
51. An antibody, or one of its functional "divalent fragments", capable of being obtained by a process as claimed in claim 50.
52. The antibody of claims 3-27, 30, 31, 34, 35, 38, 39, 42-45 and 51 as a medicament.
53. A composition comprising by way of active principle a compound 99

consisting of an antibody, or one of its functional "divalent fragments" or derivatives, as claimed in one of claims 3-27, 30, 31, 34, 35, 38, 39, 42-45 and 51 or produced by hybridoma according to claims 28, 29, 32, 33, 36, 37, 40 or 41.
54. The composition of claim 53, characterized in that it comprises, moreover, as a combination product for simultaneous, separate or sequential use, an anti-tumoral antibody.
55. The composition of claim 53 or 54, characterized in that it comprises, moreover, as a combination product for simultaneous, separate or sequential use, a cytotoxic/cytostatic agent.
56. The composition of one of the claims 53 to 55, characterized in that one, at least, of said antibodies, or one of its functional "divalent fragments" or "derivatives", is conjugated with a cell toxin and/or a radioelement.
57. The composition of claim 55, characterized in that said cytotoxic/cytostatic agent or said toxin and/or a radioelement is coupled chemically to at least one of the elements of said composition for simultaneous use.
58. The composition as claimed in one of claims 53 to 57 as a medicament.
59. The use of an antibody, or one of its functional "divalent fragments" or "derivatives", of claims 3-27, 30, 31, 34, 35, 38, 39, 42-45 and 51 or of an antibody produced by hybridoma of claims 28, 29, 32, 33, 36, 37, 40 or 41 and/or of a composition of claims 53 to 58 for the preparation of a medicament intended to inhibit the growth and/or the proliferation of tumor cells.
60. The use of an antibody, or one of its functional "divalent fragments" or "derivatives", of claims 3-27, 30, 31, 34, 35, 38, 39, 42-45 and 51 or of an antibody produced by hybridoma of claims 28, 29, 32, 33, 36, 37, 40 or 41 and/or of a composition of claims 53 to 58, or the use of claim 59, for the preparation of a medicament intended for the prevention or for the treatment of cancer.
61. The use of claim 60, characterized in that said cancer is a cancer chosen from prostate cancer, osteosarcomas, lung cancer, breast cancer, endometrial cancer, glyoblastoma or colon cancer.
62. The use of claim 60 or 61, characterized in that said cancer is a HGF dependent and independent Met-activation related cancer.
63. A method of in vitro diagnosis of illnesses induced by an overexpression or 100

an underexpression of the c-Met receptor starting from a biological sample in which the abnormal presence of c-Met receptor is suspected, characterized in that said method comprises a step wherein said biological sample is contacted with an antibody of claims 3-27, 30, 31, 34, 35, 38, 39, 42-45 and 51 or produced by hybridoma of claims 28, 29, 32, 33, 36, 37, 40 or 41, it being possible for said antibody to be, if necessary, labeled.