Antibodies that specifically block the biological activity of kidney associated antigen 1 (KAAG1)
View Patent ↗Novel monoclonal antibodies that specifically bind to KAAG1 are described. In some embodiments, the antibodies block the biological activity of KAAG1 and are useful in composition in certain cancers, more particularly in cancers that have increased cell surface expression of KAAG1, such as ovarian, renal, lung, colorectal, breast, brain, and prostate cancer, as well as melanoma. The invention also relates to cells expressing the monoclonal antibodies and antigen binding fragments such as humanized and chimeric antibodies. Additionally, method of detecting and treating cancer using the antibodies and fragments are also disclosed.
1. A method of treating ovarian cancer comprising cells expressing Kidney associated antigen 1 (KAAG1; SEQ ID NO.:2) in a subject, the method comprising administering an isolated antibody or antigen binding fragment thereof capable of binding to KAAG1 to the subject wherein the antibody or antigen binding fragment thereof is selected from the group consisting of antibodies and antigen binding fragment thereof comprising:
a. A heavy chain variable region comprising a CDRH3 having the sequence of SEQ ID NO.: 32, a CDRH1 having the sequence of SEQ ID NO.: 30 and a CDRH2 having the sequence of SEQ ID NO.:31 and a light chain variable region comprising a CDRL3 having the sequence of SEQ ID NO.:29, a CDRL1 having the sequence of SEQ ID NO.:27 and a CDRL2 having the sequence of SEQ ID NO.:28;
b. A heavy chain variable region comprising the sequence set forth in SEQ ID NO.:18 and a light chain variable region comprising the sequence set forth in SEQ ID NO.:16;
c. A heavy chain comprising the sequence set forth in SEQ ID NO.:6 and a light chain comprising the sequence set forth in SEQ ID NO.:4;
d. A heavy chain variable region comprising the sequence set forth in SEQ ID NO.:179 and a light chain variable region comprising the sequence set forth in SEQ ID NO.:178;
e. A heavy chain comprising the sequence set forth in SEQ ID NO.:177 and a light chain comprising the sequence set forth in SEQ ID NO.:176;
f. A heavy chain variable region comprising a CDRH3 having the sequence of SEQ ID NO.: 38, a CDRH1 having the sequence of SEQ ID NO.: 36 and a CDRH2 having the sequence of SEQ ID NO.:37 and a light chain variable region comprising a CDRL3 having the sequence of SEQ ID NO.:35, a CDRL1 having the sequence of SEQ ID NO.:33 and a CDRL2 having the sequence of SEQ ID NO.:34;
g. A heavy chain variable region comprising the sequence set forth in SEQ ID NO.:22 and a light chain variable region comprising the sequence set forth in SEQ ID NO.:20; and;
h. A heavy chain comprising the sequence as set forth in SEQ ID NO.:10 and a light chain comprising the sequence as set forth in SEQ ID NO.:8.
2. The method of claim 1 a. or f., wherein the antibody or antigen binding fragment thereof comprises framework amino acids of a human antibody.
3. The method of claim 1 , wherein the ovarian cancer is recurrent ovarian cancer.
4. The method of claim 1 , wherein the ovarian cancer is metastatic.
5. A method for reducing metastasis of ovarian tumor cells expressing Kidney associated antigen 1 (KAAG1; SEQ ID NO.:2) in a subject, the method comprising administering a monoclonal antibody or antigen binding fragment thereof capable of specific binding to an epitope located between amino acids 36 to 60 of KAAG1 to the subject.
6. The method of claim 5 , wherein the ovarian cancer is recurrent ovarian cancer.
7. The method of claim 5 , wherein the ovarian cancer is metastatic.
8. The method of claim 7 , wherein the antibody or antigen binding fragment thereof binds to KAAG1 at a surface of tumor cells, induces lysis of tumor cells, reduces spreading of tumor cells, decreases formation of tumor or decreases metastasis of tumor cells.
9. The method of claim 1 , wherein the antibody or antigen binding fragment thereof comprises a heavy chain variable region comprising the sequence set forth in SEQ ID NO.:179 and a light chain variable region comprising the sequence set forth in SEQ ID NO.:178.
10. The method of claim 1 , wherein the antibody or antigen binding fragment thereof comprises a heavy chain variable region as defined in SEQ ID NO.:18 and a light chain variable region as defined in SEQ ID NO.: 16.
11. The method of claim 1 , wherein the antibody or antigen binding fragment thereof is conjugated with a cytotoxic moiety.
12. The method of claim 5 , wherein the antibody or antigen binding fragment thereof is conjugated with a cytotoxic moiety.
13. The method of claim 10 , wherein the antibody or antigen binding fragment thereof is conjugated with a cytotoxic moiety.
14. The method of claim 9 , wherein the antibody or antigen binding fragment thereof is conjugated with a cytotoxic moiety.
15. The method of claim 5 , wherein the monoclonal antibody or antigen binding fragment thereof is a chimeric antibody, a humanized antibody, a human antibody or an antigen binding fragment thereof.
16. The method of claim 12 , wherein the monoclonal antibody or antigen binding fragment thereof is a chimeric antibody, a humanized antibody, a human antibody or an antigen binding fragment thereof.
17. A method of treating ovarian cancer comprising cells expressing Kidney associated protein 1 (KAAG1: SEQ ID NO.:2) in a subject, the method comprising administering a monoclonal antibody or an antigen binding fragment thereof, that is capable of specific binding to at least 10 contiguous amino acids of amino acid residues 36 to 60 of SEQ ID NO.:2 to the subject.
18. The method of claim 17 , wherein the monoclonal antibody or antigen binding fragment thereof is a chimeric antibody, a humanized antibody, a human antibody or an antigen binding fragment thereof.
19. The method of claim 17 , wherein the monoclonal antibody or antigen binding fragment thereof is conjugated with a cytotoxic moiety.
20. The method of claim 18 , wherein the antibody or antigen binding fragment thereof is conjugated with a cytotoxic moiety.