Anti-TIM-3 antibodies and compositions
This invention relates to anti-TIM-3 antibodies and antibody compositions and their use in enhancing immunity in a patient, e.g., to treat cancer.
1. An anti-TIM-3 antibody or an antigen-binding portion thereof, wherein said antibody comprises H-CDR1-3 and L-CDR1-3 amino acid sequences of SEQ ID NOs: 7-12, respectively.
2. The anti-TIM-3 antibody or antigen-binding portion of claim 1 , wherein said antibody comprises a heavy chain (HC) and a light chain (LC) whose variable domains have the amino acid sequences of:
a) SEQ ID NOs: 15 and 4, respectively; or
b) SEQ ID NOs: 3 and 4, respectively.
3. The anti-TIM-3 antibody of claim 2 , wherein said HC and said LC further comprise the amino acid sequences of:
a) SEQ ID NOs: 5 and 6, respectively;
b) SEQ ID NOs: 25 and 6, respectively;
c) SEQ ID NOs: 23 and 6, respectively; or
d) SEQ ID NOs: 24 and 6, respectively.
4. An anti-TIM-3 antibody that comprises a heavy chain comprising the amino acid sequences of SEQ ID NOs: 15 and 25 and a light chain comprising the amino acid sequences of SEQ ID NOs: 4 and 6.
5. The anti-TIM-3 antibody or antigen-binding portion of claim 1 , wherein the antibody or portion has at least one of the following properties:
a) binds to human TIM-3 with a K D of 23 nM or less as measured by surface plasmon resonance;
b) binds to cynomolgus TIM-3 with a K D of 22 nM or less as measured by surface plasmon resonance;
c) binds to human TIM-3 with an EC50 of 1.2 nM or less as measured by ELISA;
d) binds to cynomolgus TIM-3 with an EC50 of 46 nM or less as measured by ELISA;
e) increases IFN-γ secretion in a one-way mixed lymphocyte reaction assay;
f) increases IFN-γ secretion in a two-way mixed lymphocyte reaction assay;
g) increases TNF-α secretion in a one-way mixed lymphocyte reaction assay;
h) increases TNF-α secretion from dendritic cells; and
i) inhibits interaction of TIM-3 with phosphatidylserine.
6. A pharmaceutical composition comprising an anti-TIM-3 antibody or antigen-binding portion of claim 1 and a pharmaceutically acceptable excipient.
7. An isolated nucleic acid molecule or isolated nucleic acid molecules comprising a nucleotide sequence that encodes the heavy chain or an antigen-binding portion thereof, and a nucleotide sequence that encodes the light chain or an antigen-binding portion thereof, nucleotide sequence that encodes the light chain or an antigen-binding portion thereof, or of the anti-TIM-3 antibody of claim 1 .
8. A vector or vectors comprising the isolated nucleic acid molecule or isolated nucleic acid molecules of claim 7 , wherein said vector further comprises an expression control sequence.
9. A host cell comprising a nucleotide sequence that encodes the heavy chain or an antigen-binding portion thereof, and a nucleotide sequence that encodes the light chain or an antigen-binding portion thereof, of the anti-TIM-3 antibody of claim 1 .
10. A method for producing an anti-TIM-3 antibody or an antigen-binding portion thereof, comprising providing a host cell according to claim 9 , culturing said host cell under conditions suitable for expression of the antibody or portion, and isolating the resulting antibody or portion.
11. A bispecific binding molecule having an antigen-binding portion of an anti-TIM-3 antibody of claim 1 and an antigen-binding portion of another, distinct antibody.
12. A method for enhancing immunity in a patient in need thereof, comprising administering to said patient an anti-TIM-3 antibody or antigen-binding portion of claim 1 .
13. A method for treating cancer in a patient, comprising administering to said patient an anti-TIM-3 antibody or antigen-binding portion of claim 1 .
14. The method of claim 12 , further comprising administering to the patient a chemotherapeutic agent, an anti-neoplastic agent, an anti-angiogenic agent, a tyrosine kinase inhibitor, or a TIM-3 pathway inhibitor.
15. The method of claim 13 , wherein:
a) the cancer originates in skin, lung, intestine, ovary, brain, prostate, kidney, soft tissues, hematopoietic system, head and neck, liver, bladder, breast, stomach, uterus, or pancreas;
b) the patient has leukemia, Hodgkin's lymphoma, or non-Hodgkin's lymphoma;
c) the patient has a solid tumor; or
d) the patient has melanoma, non-small cell lung cancer, colorectal cancer, biliary tract cancer, esophageal cancer, gastric cancer, pancreatic cancer, or renal cell carcinoma.
16. A method for enhancing immunity in a patient in need thereof, comprising administering to said patient an anti-TIM-3 antibody or antigen-binding portion of claim 4 .
17. A method for treating cancer in a patient, comprising administering to said patient an anti-TIM-3 antibody or antigen-binding portion of claim 4 .
18. The method of claim 16 , further comprising administering to the patient a chemotherapeutic agent, an anti-neoplastic agent, an anti-angiogenic agent, a tyrosine kinase inhibitor, or a TIM-3 pathway inhibitor.
19. The method of claim 17 , wherein:
a) the cancer originates in skin, lung, intestine, ovary, brain, prostate, kidney, soft tissues, hematopoietic system, head and neck, liver, bladder, breast, stomach, uterus, or pancreas;
b) the patient has leukemia, Hodgkin's lymphoma, or non-Hodgkin's lymphoma;
c) the patient has a solid tumor; or
d) the patient has melanoma, non-small cell lung cancer, colorectal cancer, biliary tract cancer, esophageal cancer, gastric cancer, pancreatic cancer, or renal cell carcinoma.
20. The method of claim 12 , further comprising administering irinotecan to the patient.
21. The method of claim 15 , further comprising administering irinotecan to the patient.
22. The method of claim 16 , further comprising administering irinotecan to the patient.
23. The method of claim 19 , further comprising administering irinotecan to the patient.