Anti-PD-L1 antibodies and uses thereof
Provided herein are anti-PD-L1 antibodies and antigen-binding fragments thereof. Also provided are nucleic acids encoding the antibodies, compositions containing the antibodies, and methods of producing the antibodies and using the antibodies for treating or preventing diseases such as cancer, infectious diseases and autoimmune diseases.
1. An isolated monoclonal antibody or antigen-binding fragment thereof comprising a light chain complementarity determining region 1 (LCDR1), a LCDR2, a LCDR3, a heavy chain complementarity determining region 1 (HCDR1), a HCDR2, and a HCDR3, having the polypeptide sequences of:
(1) SEQ ID NOs: 30, 31, 32, 26, 27, and 28, respectively
(2) SEQ ID NOs: 6, 7, 8, 2, 3, and 4, respectively;
(3) SEQ ID NOs: 14, 15, 16, 10, 11, and 12, respectively;
(4) SEQ ID NOs: 22, 23, 24, 18, 19, and 20, respectively;
(5) SEQ ID NOs: 38, 39, 40, 34, 35, and 36, respectively;
(6) SEQ ID NOs: 46, 47, 48, 42, 43, and 44, respectively; or
(7) SEQ ID NOs: 54, 55, 56, 50, 51, and 52, respectively;
wherein the antibody or antigen-binding fragment thereof binds PD-L1.
2. The isolated monoclonal antibody or antigen-binding fragment of claim 1 , comprising a heavy chain variable region having a polypeptide sequence at least 95% identical to SEQ ID NO: 25, 1, 9, 17, 33, 41 or 49, or a light chain variable region having a polypeptide sequence at least 95% identical to SEQ ID NO: 29, 5, 13, 21, 37, 45 or 53.
3. The isolated monoclonal antibody or antigen-binding fragment of claim 1 , comprising:
a. a heavy chain variable region having the polypeptide sequence of SEQ ID NO: 25, and a light chain variable region having the polypeptide sequence of SEQ ID NO: 29;
b. a heavy chain variable region having the polypeptide sequence of SEQ ID NO: 1, and a light chain variable region having the polypeptide sequence of SEQ ID NO: 5;
c. a heavy chain variable region having the polypeptide sequence of SEQ ID NO: 9, and a light chain variable region having the polypeptide sequence of SEQ ID NO: 13;
d. a heavy chain variable region having the polypeptide sequence of SEQ ID NO: 17, and a light chain variable region having the polypeptide sequence of SEQ ID NO: 21;
e. a heavy chain variable region having the polypeptide sequence of SEQ ID NO: 33, and a light chain variable region having the polypeptide sequence of SEQ ID NO: 37;
f. a heavy chain variable region having the polypeptide sequence of SEQ ID NO: 41, and a light chain variable region having the polypeptide sequence of SEQ ID NO: 45; or
g. a heavy chain variable region having the polypeptide sequence of SEQ ID NO: 49, and a light chain variable region having the polypeptide sequence of SEQ ID NO: 53.
4. The isolated monoclonal antibody or antigen-binding fragment of claim 1 , wherein the antibody or antigen-binding fragment thereof is chimeric.
5. The isolated monoclonal antibody or antigen-binding fragment of claim 1 , wherein the antibody or antigen-binding fragment thereof is human.
6. The isolated monoclonal antibody or antigen-binding fragment of claim 4 , comprising a human heavy chain IgG4 constant region having a S228P mutation, and a human antibody light chain kappa constant region.
7. An isolated nucleic acid encoding the monoclonal antibody or antigen-binding fragment of claim 1 .
8. A vector comprising the isolated nucleic acid of claim 7 .
9. An isolated host cell comprising the vector of claim 8 .
10. A pharmaceutical composition, comprising the isolated monoclonal antibody or antigen-binding fragment of claim 1 and a pharmaceutically acceptable carrier.
11. A method of blocking binding of PD-L1 to PD-1 and/or B7.1, or augmenting secretion of IFN-γ and IL-2 in a subject in need thereof, comprising administering to the subject the pharmaceutical composition of claim 10 .
12. A method of treating an infectious disease or a graft versus host disease in a subject in need thereof, comprising administering to the subject the pharmaceutical composition of claim 10 .
13. A method of treating a tumor in a subject in need thereof, comprising administering to the subject the pharmaceutical composition of claim 10 , wherein the tumor is selected from the group consisting of a solid tumor, a hematologic cancer, bladder cancer, brain cancer, breast cancer, colon cancer, gastric cancer, glioma, head cancer, leukemia, liver cancer, lung cancer, lymphoma, myeloma, neck cancer, ovarian cancer, melanoma, pancreatic cancer, renal cancer, salivary cancer, stomach cancer, thymic epithelial cancer, and thyroid cancer.
14. A method of producing the monoclonal antibody or antigen-binding fragment of claim 1 , comprising culturing a cell comprising a nucleic acid encoding the monoclonal antibody or antigen-binding fragment under conditions to produce the monoclonal antibody or antigen-binding fragment, and recovering the antibody or antigen-binding fragment from the cell or cell culture.
15. A method of producing a pharmaceutical composition comprising the monoclonal antibody or antigen-binding fragment of claim 1 , comprising combining the monoclonal antibody or antigen-binding fragment with a pharmaceutically acceptable carrier to obtain the pharmaceutical composition.