Anti-PD-L1 antibodies and uses thereof
Provided are anti-PD-L1 antibodies or fragments thereof. The antibodies or fragments thereof specifically bind to the immunoglobulin C domain of the PD-L1 protein. In various example, the antibodies or fragments thereof include a VH CDR1 of SEQ ID NO: 1, a VH CDR2 of SEQ ID NO: 2, a VH CDR3 of SEQ ID NO: 3, a VL CDR1 of SEQ ID NO: 4, a VL CDR2 of SEQ ID NO: 5, and a VL CDR3 of SEQ ID NO: 6, or variants of each thereof. Methods of using the antibodies or fragments thereof for treating and diagnosing diseases such as cancer and infectious diseases are also provided.
1. An antibody or antigen-binding fragment thereof, wherein the antibody or fragment thereof can specifically bind to a human Programmed death-ligand 1 (PD-L1) protein, and comprises a heavy chain variable region (VH) comprising a heavy chain complementarity determining region 1 (VH CDR1), a VH CDR2, and a VH CDR3 having the VH CDR1, VH CDR2 and VH CDR3 of SEQ ID NO:20, respectively, and a light chain variable region (VL) comprising a VL CDR1, a VL CDR2, and a VL CDR3 having the VL CDR1, VL CDR2 and VL CDR3 of SEQ ID NO:28, respectively.
2. A composition comprising the antibody or fragment thereof of claim 1 and a pharmaceutically acceptable carrier.
3. An isolated cell comprising one or more polynucleotide encoding the antibody or fragment thereof of claim 1 .
4. A method of treating cancer or infection in a patient in need thereof, comprising administering to the patient an effective amount of the antibody or fragment thereof of claim 1 .
5. The method of claim 4 , wherein the cancer is a solid tumor.
6. The method of claim 5 , wherein the cancer is selected from the group consisting of bladder cancer, liver cancer, colon cancer, rectal cancer, endometrial cancer, leukemia, lymphoma, pancreatic cancer, small cell lung cancer, non-small cell lung cancer, breast cancer, urethral cancer, head and neck cancer, gastrointestinal cancer, stomach cancer, oesophageal cancer, ovarian cancer, renal cancer, melanoma, prostate cancer and thyroid cancer.
7. The method of claim 5 , further comprising administering to the patient a second cancer therapeutic agent.
8. The method of claim 4 , wherein the infection is viral infection, bacterial infection, fungal infection or infection by a parasite.
9. A method of treating cancer or infection in a patient in need thereof, comprising:
(a) treating a T cell, in vitro, with the antibody or fragment thereof of claim 1 ; and
(b) administering the treated T cell to the patient.
10. The method of claim 9 , further comprising, prior to step (a), isolating the T cell from an individual.
11. The method of claim 10 , wherein the T cell is isolated from the patient.
12. The method of claim 10 , wherein the T cell is isolated from a donor individual different from the patient.
13. The method of claim 9 , wherein the T cell is a tumor-infiltrating T lymphocyte, a CD4+ T cell, a CD8+ T cell, or a combination thereof.
14. An isolated bispecific antibody comprising a fragment of claim 1 and a second antigen-binding fragment having specificity to a molecule on an immune cell.
15. The bispecific antibody of claim 14 , wherein the molecule is selected from the group consisting of PD-1, CTLA-4, LAG-3, CD28, CD122, 4-1BB, TIM3, OX-40, OX40L, CD40, CD40L, LIGHT, ICOS, ICOSL, GITR, GITRL, TIGIT, CD27, VISTA, B7H3, B7H4, HEVM, BTLA, KIR, and CD47.
16. The antibody or fragment thereof of claim 1 , wherein the VH CDR1, VH CDR2, VH CDR3, VL CDR1, VL CDR2 and VL CDR3 are defined according to Kabat numbering.
17. The antibody or fragment thereof of claim 1 , wherein the VH comprises the SEQ ID NO:20 and the VL comprises the amino acid sequence of SEQ ID NO:28.
18. The antibody or fragment thereof of claim 1 , wherein the antibody or fragment thereof can specifically bind to an immunoglobulin C (Ig C) domain of the PD-L1 protein at amino acid residues Y134, K162, and N183, and does not specifically bind to an immunoglobulin V (Ig V) domain of the PD-L1 protein.