IP Library Granted Patent US 10,973,915
Granted Patent B2
US 10,973,915 · App. 15/747,504 · Granted Apr 13, 2021

Anti-PD-1 antibodies and uses thereof

Inventors: Lile Liu (Shanghai, CN); Xinxiu Yang (Shanghai, CN); Haishan Luo (Shanghai, CN); Hu Liu (Shanghai, CN); Zhengrong Shuai (Shanghai, CN); Jian Wang (Shanghai, CN); Qin Zhong (Shanghai, CN); Qing Duan (Shanghai, CN); Hongzhuan Gu (Shanghai, CN); Tatchi Teddy Yang (Shanghai, CN)
Assignee: SHANGHAI YUNYI HEALTHCARE AND TECHNOLOGY CO., LTD.
A61K39/39558A61K39/39591A61P35/00C07K16/2803C07K16/2818C07K2317/21C07K2317/24C07K2317/33C07K2317/732C07K2317/734C07K2317/76C07K2317/92C07K2317/94
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Quick Facts
Patent No.
US 10,973,915
App. No.
15/747,504
Granted
Apr 13, 2021
Kind
B2
Abstract

Anti-PD-1 antibodies and antigen-binding fragments thereof are described. Also described are nucleic acids encoding the antibodies, compositions comprising the antibodies, and methods of producing the antibodies and using the antibodies for treating or preventing diseases such as cancers and autoimmune diseases.

Claims (18)

1. An isolated monoclonal antibody or antigen-binding fragment thereof comprising LCDR1, LCDR2, LCDR3, HCDR1, HCDR2 and HCDR3, having the polypeptide sequences of:

SEQ ID NOs: 30, 31, 32, 26, 27, and 28, respectively;

wherein the antibody or antigen-binding fragment thereof binds programmed cell death protein-1 (PD-1).

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 or a light chain variable region having a polypeptide sequence at least 95% identical to SEQ ID NO: 29.

3. The isolated monoclonal antibody or antigen-binding fragment of claim 1 , comprising:

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.

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 5 , 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. A host cell comprising the nucleic acid of claim 7 .

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-1 to programmed cell death-ligand 1 (PD-L1) or programmed cell death-ligand 2 (PD-L2), 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 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, biliary cancer, brain cancer, breast cancer, colon cancer, esophageal 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 and the tumor cell thereof expresses PD-L1.

13. 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.

14. 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.

15. 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 colon cancer, esophageal cancer, gastric cancer, glioma, head cancer, leukemia, liver cancer, lung cancer, lymphoma, myeloma, neck cancer, ovarian cancer, melanoma, pancreatic cancer, renal cancer, salivary cancer and stomach cancer; and the tumor cell thereof expresses PD-L1.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 13, 2020
From: PHARMAEXPLORER LIMITED
To: SHANGHAI YUNYI HEALTHCARE AND TECHNOLOGY CO., LTD.
Reel/Frame 052109/0483 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 3, 2018
From: LIU, LILE; YANG, XINXIU; LUO, HAISHAN; LIU, HU; SHUAI, ZHENGRONG; WANG, JIAN; ZHONG, QIN; DUAN, QING; GU, HONGZHUAN; YANG, TATCHI TEDDY
To: PHARMAEXPLORER LIMITED
Reel/Frame 045707/0553 →
Priority Claims (1)
CN 201510451773.6 · Jul 28, 2015 · national
Continuity (1)
Related Publication 20180214548A1 · Aug 2, 2018