IP Library › Granted Patent US 11,560,430
Granted Patent B2
US 11,560,430 · App. 16/543,310 · Granted Jan 24, 2023

Anti-PD-1 antibodies and uses thereof

Inventors: Lieping Chen (Beijing, CN); Liqun Luo (Beijing, CN)
Assignee: Tayu Huaxia Biotech Medical Group Co., LTD
C07K16/2827A61P19/02A61P31/00A61P35/00A61P37/00A61P37/02C07K16/2818C12N15/63C12N15/85A61K2039/505C07K2317/21C07K2317/24C07K2317/33C07K2317/52C07K2317/565C07K2317/73C07K2317/76C07K2317/92C12N2015/8518
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Quick Facts
Patent No.
US 11,560,430
App. No.
16/543,310
Granted
Jan 24, 2023
Kind
B2
Abstract

Provided are anti-PD-1 antibodies or fragments thereof. In various example, the antibodies or fragments thereof includes a heavy chain variable region comprising heavy chain complementarity determining regions HCDR1, HCDR2, and HCDR3, and a light chain variable region comprising light chain complementarity determining regions LCDR1, LCDR2, and LCDR3. Methods of using the antibodies or fragments thereof for treating and diagnosing diseases such as cancer, infection or immune disorders are also provided.

Claims (34)

1. A method of treating a cancer in an individual in need thereof, comprising administering to the individual a composition comprising an effective amount of antibody or fragment thereof that specifically binds to PD-1,

wherein the antibody or fragment thereof comprises a heavy chain variable region comprising heavy chain complementarity determining regions HCDR1, HCDR2, and HCDR3, and a light chain variable region comprising light chain complementarity determining regions LCDR1, LCDR2, and LCDR3, wherein the HCDR1, HCDR2, HCDR3, LCDR1, LCDR2, and LCDR3 are selected from the group consisting of:

(a) HCDR1: GFTFSSYT (SEQ ID NO: 1), HCDR2: ISHGGGDT (SEQ ID NO: 2), HCDR3: ARHSGYERGYYYVMDY (SEQ ID NO: 3), LCDR1: ESVDYYGFSF (SEQ ID NO: 4), LCDR2: AAS (SEQ ID NO: 5), LCDR3: QQSKEVPW (SEQ ID NO: 6);

(b) HCDR1: GYTFTSYT (SEQ ID NO: 7), HCDR2: INPTTGYT (SEQ ID NO: 8), HCDR3: ARDDAYYSGY (SEQ ID NO: 9), LCDR1: ENIYSNL (SEQ ID NO: 10), LCDR2: AAK (SEQ ID NO: 11), LCDR3: QHFWGTPWT (SEQ ID NO: 12); and

(c) HCDR1: GFAFSSYD (SEQ ID NO: 13), HCDR2: ITIGGGTT (SEQ ID NO: 14), HCDR3: ARHRYDYFAMDN (SEQ ID NO: 15), LCDR1: ENVDNYGINF (SEQ ID NO: 16), LCDR2: VSS (SEQ ID NO: 17), LCDR3: QQSKDVPW (SEQ ID NO: 18).

2. The method of claim 1 , wherein the antibody or fragment thereof comprises a heavy chain constant region, a light chain constant region, an Fc region, or the combination thereof.

3. The method of claim 2 , wherein the light chain constant region is a kappa or lambda chain constant region.

4. The method of claim 1 , wherein the antibody or fragment thereof is of an isotype of IgG, IgM, IgA, IgE or IgD.

5. The method of claim 4 , wherein the antibody or fragment thereof has an isotype of IgG1, IgG2, IgG3 or IgG4.

6. The method of claim 1 , wherein the antibody or fragment thereof is a chimeric antibody or a humanized antibody.

7. The method of claim 6 , wherein the antibody or fragment thereof is a humanized antibody.

8. The method of claim 1 , wherein the antibody or fragment thereof comprises a heavy chain variable region comprising the amino acid sequence of SEQ ID NO: 35, SEQ ID NO: 37, or SEQ ID NO: 39, or an amino acid sequence having at least 80% sequence identity to SEQ ID NO: 35, SEQ ID NO: 37, or SEQ ID NO: 39.

9. The method of claim 1 , wherein the antibody or fragment thereof comprises a light chain variable region comprising the amino acid sequence of SEQ ID NO: 41, SEQ ID NO: 43, or SEQ ID NO: 45, or an amino acid sequence having at least 80% sequence identity to SEQ ID NO: 41, SEQ ID NO: 43, or SEQ ID NO: 45.

10. The method of claim 8 , wherein the antibody or fragment thereof comprises a light chain variable region comprising the amino acid sequence of SEQ ID NO: 41, SEQ ID NO: 43, or SEQ ID NO: 45, or an amino acid sequence having at least 80% sequence identity to SEQ ID NO: 41, SEQ ID NO: 43, or SEQ ID NO: 45.

11. The method of claim 1 , wherein the antibody or fragment thereof comprises:

(a) a heavy chain variable region comprising the amino acid sequence of SEQ ID NO: 35, and a light chain variable region comprising the amino acid sequence of SEQ ID NO: 41;

(b) a heavy chain variable region comprising the amino acid sequence of SEQ ID NO: 37, and a light chain variable region comprising the amino acid sequence of SEQ ID NO: 43; or

(c) a heavy chain variable region comprising the amino acid sequence of SEQ ID NO: 39, and a light chain variable region comprising the amino acid sequence of SEQ ID NO: 45.

12. The method of claim 1 , wherein the individual is a human.

13. A method of treating an infection in an individual in need thereof, comprising administering to the individual a composition comprising an effective amount of antibody or fragment thereof that specifically binds to PD-1, wherein the antibody or fragment thereof comprises a heavy chain variable region comprising heavy chain complementarity determining regions HCDR1, HCDR2, and HCDR3, and a light chain variable region comprising light chain complementarity determining regions LCDR1, LCDR2, and LCDR3, and wherein the HCDR1, HCDR2, HCDR3, LCDR1, LCDR2, and LCDR3 are selected from the group consisting of:

(a) HCDR1: GFTFSSYT (SEQ ID NO: 1), HCDR2: ISHGGGDT (SEQ ID NO: 2), HCDR3: ARHSGYERGYYYVMDY (SEQ ID NO: 3), LCDR1: ESVDYYGFSF (SEQ ID NO: 4), LCDR2: AAS (SEQ ID NO: 5), LCDR3: QQSKEVPW (SEQ ID NO: 6);

(b) HCDR1: GYTFTSYT (SEQ ID NO: 7), HCDR2: INPTTGYT (SEQ ID NO: 8), HCDR3: ARDDAYYSGY (SEQ ID NO: 9), LCDR1: ENIYSNL (SEQ ID NO: 10), LCDR2: AAK (SEQ ID NO: 11), LCDR3: QHFWGTPWT (SEQ ID NO: 12); and

(c) HCDR1: GFAFSSYD (SEQ ID NO: 13), HCDR2: ITIGGGTT (SEQ ID NO: 14), HCDR3: ARHRYDYFAMDN (SEQ ID NO: 15), LCDR1: ENVDNYGINF (SEQ ID NO: 16), LCDR2: VSS (SEQ ID NO: 17), LCDR3: QQSKDVPW (SEQ ID NO: 18).

14. A method of treating an immune disorder in an individual in need thereof, comprising administering to the individual a composition comprising an effective amount of antibody or fragment thereof that specifically binds to PD-1,_wherein the antibody or fragment thereof comprises a heavy chain variable region comprising heavy chain complementarity determining regions HCDR1, HCDR2, and HCDR3, and a light chain variable region comprising light chain complementarity determining regions LCDR1, LCDR2, and LCDR3, and wherein the HCDR1, HCDR2, HCDR3, LCDR1, LCDR2, and LCDR3 are selected from the group consisting of:

(a) HCDR1: GFTFSSYT (SEQ ID NO: 1), HCDR2: ISHGGGDT (SEQ ID NO: 2), HCDR3: ARHSGYERGYYYVMDY (SEQ ID NO: 3), LCDR1: ESVDYYGFSF (SEQ ID NO: 4), LCDR2: AAS (SEQ ID NO: 5), LCDR3: QQSKEVPW (SEQ ID NO: 6);

(b) HCDR1: GYTFTSYT (SEQ ID NO: 7), HCDR2: INPTTGYT (SEQ ID NO: 8), HCDR3: ARDDAYYSGY (SEQ ID NO: 9), LCDR1: ENIYSNL (SEQ ID NO: 10), LCDR2: AAK (SEQ ID NO: 11), LCDR3: QHFWGTPWT (SEQ ID NO: 12); and

(c) HCDR1: GFAFSSYD (SEQ ID NO: 13), HCDR2: ITIGGGTT (SEQ ID NO: 14), HCDR3: ARHRYDYFAMDN (SEQ ID NO: 15), LCDR1: ENVDNYGINF (SEQ ID NO: 16), LCDR2: VSS (SEQ ID NO: 17), LCDR3: QQSKDVPW (SEQ ID NO: 18).

15. The method of claim 1 , wherein the antibody or fragment thereof is administered intravenously.

16. The method of claim 1 , wherein the method further comprises administering a second therapy.

17. A method of treating a cancer in an individual in need thereof, comprising administering to the individual a composition comprising an effective amount of antibody or fragment thereof that specifically binds to PD-1,

and wherein the antibody or fragment thereof is selected from the group comprising:

(a) a HCDR1, a HCDR2, and a HCDR3, respectively comprising the amino acid sequences of a CDR1, a CDR2, and a CDR3 within a VH chain having the sequence set forth SEQ ID NOs: 35, and a LCDR1, a LCDR2, and a LCDR3, respectively comprising the amino acid sequences of a CDR1, a CDR2, and a CDR3 within a VL chain having the sequence set forth in SEQ ID NO: 41;

(b) a HCDR1, a HCDR2, and a HCDR3, respectively comprising the amino acid sequences of a CDR1, a CDR2, and a CDR3 within a VH chain having the sequence set forth in SEQ ID NO: 37, and a LCDR1, a LCDR2, and a LCDR3, respectively comprising the amino acid sequence of a CDR1, a CDR2, and a CDR3 within a VL chain having the sequence set forth in SEQ ID NO: 43;

(c) a HCDR1, a HCDR2, and a HCDR3, respectively comprising the amino acid sequences of a CDR1, a CDR2, and a CDR3 within a VH chain having the sequence set forth in SEQ ID NO: 39, and a LCDR1, a LCDR2, and a LCDR3, respectively comprising the amino acid sequences of a CDR1, a CDR2, and a CDR3 within a VL chain having the sequence set forth in SEQ ID NO: 45.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 20, 2019
From: CHEN, LIEPING; LUO, LIQUN
To: TAYU HUAXIA BIOTECH MEDICAL GROUP CO., LTD
Reel/Frame 050110/0227 →
Priority Claims (1)
CN 201710046148.2 · Jan 20, 2017 · national
Continuity (3)
Continuation 16252418 · Jan 18, 2019
Continuation PCTCN2018073383 · Jan 19, 2018
Related Publication 20200115454A1 · Apr 16, 2020
Cited By (1)
US 12,258,407