Antibodies against kidney associated antigen 1 and antigen binding fragments thereof
View Patent ↗Novel antibodies and antigen binding fragments that specifically bind to KAAG1 and which may be used in the treatment, detection and diagnosis of cancer comprising KAAG1-expressing cells are disclosed herein. Cells expressing the antibodies and antigen binding fragments as well as methods of detecting and treating cancer using the antibodies and fragments are also disclosed. Cancer indications which may benefit from such treatment or detection include ovarian cancer, renal cancer, lung cancer, colorectal cancer, breast cancer, brain cancer, and prostate cancer, as well as melanomas.
1. An antibody or antigen binding fragment thereof having a heavy chain variable region comprising the complementarity determining region amino acid sequences set forth in SEQ ID NO.:5, SEQ ID NO.:6 and SEQ ID NO.:7 and a light chain variable region comprising the complementarity determining region amino acid sequences set forth in SEQ ID NO.:8, SEQ ID NO.:9 and SEQ ID NO.:10.
2. The antibody or antigen binding fragment of claim 1 , wherein the antibody is a monoclonal antibody, a chimeric antibody, an hybrid antibody, a humanized antibody, a human antibody or an antigen binding fragment thereof.
3. The antibody or antigen binding fragment of claim 1 , wherein the light chain variable region is as set forth in SEQ ID NO.:30, SEQ ID NO.:31, SEQ ID NO.:32, SEQ ID NO.:33, SEQ ID NO.:34 or SEQ ID NO.:4 and wherein the heavy chain variable region is as set forth in SEQ ID NO.:35, SEQ ID NO.:36, SEQ ID NO.:37, SEQ ID NO.:38, SEQ ID NO.:39, SEQ ID NO.:40, SEQ ID NO.:41 or SEQ ID NO.:2.
4. An antibody or antigen binding fragment thereof, comprising the light chain variable region set forth in SEQ ID NO.:33 or in SEQ ID NO.:34 and the heavy chain variable region set forth in SEQ ID NO.:38, SEQ ID NO.:39, SEQ ID NO.:40 or SEQ ID NO.:41.
5. The antibody or antigen binding fragment of claim 4 , wherein the antibody or antigen binding fragment comprises:
a. The heavy chain variable region set forth in SEQ ID NO.:41 and the light chain variable region set forth in SEQ ID NO.:33;
b. The heavy chain set forth in SEQ ID NO.:49 and the light chain set forth in SEQ ID NO.:43;
c. The heavy chain variable region set forth in SEQ ID NO.:41 and the light chain variable region set forth in SEQ ID NO.:34, or;
d. The heavy chain set forth in SEQ ID 49 and the light chain set forth in SEQ ID NO.:44.
6. The antibody or antigen binding fragment of claim 1 , conjugated with a therapeutic moiety or with a detectable moiety.
7. A pharmaceutical composition comprising an antibody or antigen binding fragment thereof having a heavy chain variable region comprising the complementarity determining region amino acid sequences set forth in SEQ ID NO.:5, SEQ ID NO.:6 and SEQ ID NO.:7 and a light chain variable region comprising the complementarity determining region amino acid sequences set forth in SEQ ID NO.:8, SEQ ID NO.:9 and SEQ ID NO.:10, and a pharmaceutically acceptable carrier.
8. The antibody or antigen binding fragment thereof of claim 5 , conjugated with a therapeutic moiety.
9. The pharmaceutical composition of claim 7 , wherein the antibody is a monoclonal antibody, a chimeric antibody, an hybrid antibody, a humanized antibody or a human antibody or an antigen binding fragment thereof.
10. The pharmaceutical composition of claim 7 , wherein the antibody or antigen binding fragment comprises a light chain variable region as set forth in SEQ ID NO.:33 or SEQ ID NO.:34 and a heavy chain variable region as set forth in SEQ ID NO.:38, SEQ ID NO.:39, SEQ ID NO.:40 or SEQ ID NO.:41.
11. The pharmaceutical composition of claim 10 , wherein the antibody or antigen binding fragment thereof comprises:
a. a heavy chain variable region as set forth in SEQ ID NO.:41 and a light chain variable region as set forth in SEQ ID NO.:33;
b. The heavy chain set forth in SEQ ID NO.:49 and the light chain set forth in SEQ ID NO.:43;
c. A heavy chain variable region as set forth in SEQ ID NO.:41 and a light chain variable region as set forth in SEQ ID NO.:34, or;
d. The heavy chain set forth in SEQ ID 49 and the light chain set forth in SEQ ID NO.:44.
12. The pharmaceutical composition of claim 7 , wherein the antibody or antigen binding fragment is conjugated with a therapeutic moiety.
13. The antibody or antigen binding fragment of claim 6 , wherein the therapeutic moiety comprises a cytotoxic agent.
14. The antibody or antigen binding fragment of claim 13 , wherein the cytotoxic agent comprises an auristatin.
15. The antibody or antigen binding fragment of claim 14 , wherein the auristatin comprises monomethyl auristatin E or monomethyl auristatin F.
16. The antibody or antigen binding fragment of claim 15 , wherein the antibody or antigen binding fragment comprises:
a. The heavy chain variable region set forth in SEQ ID NO.:41 and the light chain variable region set forth in SEQ ID NO.:33, or;
b. The heavy chain set forth in SEQ ID NO.:49 and the light chain set forth in SEQ ID NO.:43.
17. The pharmaceutical composition of claim 12 , wherein the therapeutic moiety comprises a cytotoxic agent.
18. The pharmaceutical composition of claim 17 , wherein the cytotoxic agent comprises an auristatin.
19. The pharmaceutical composition of claim 18 , wherein the auristatin comprises monomethyl auristatin E or monomethyl auristatin F.
20. The pharmaceutical composition of claim 19 , wherein the antibody or antigen binding fragment comprises:
a. The heavy chain variable region set forth in SEQ ID NO.:41 and the light chain variable region set forth in SEQ ID NO.:33, or;
b. The heavy chain set forth in SEQ ID NO.:49 and the light chain set forth in SEQ ID NO.:43.