IP Library Granted Patent US 10,556,947
Granted Patent B2
US 10,556,947 · App. 15/627,305 · Granted Feb 11, 2020

Binding molecule that binds specifically to the precursor of brain-derived neurotrophic factor

Inventors: Changqi Li (Shanghai, CN); Huamao Wang (Shanghai, CN); Ruping Dai (Shanghai, CN); Xiumei Cai (Shanghai, CN); Xinfu Zhou (Shanghai, CN)
Assignee: Shanghai Yile Biotechnology Co., Ltd.
C07K16/22A61K2039/505A61K2039/545C07K2317/51C07K2317/515C07K2317/56C07K2317/565C07K2317/76
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Quick Facts
Patent No.
US 10,556,947
App. No.
15/627,305
Granted
Feb 11, 2020
Kind
B2
Abstract

Disclosed herein is use of a binding molecule which specifically binds to a precursor of brain-derived neurotrophic factor (proBDNF). The binding molecule for proBDNF, especially a monoclonal antibody against proBDNF, can be used to prevent, mitigate or treat autoimmune diseases.

Claims (17)

1. A method for mitigating or treating rheumatoid arthritis comprising administering to a subject in need thereof a binding molecule which specifically binds to a precursor of brain-derived neurotrophic factor, wherein the binding molecule is a monoclonal antibody comprising a heavy chain variable region having a CDR1 region with at least 95% sequence homology to SEQ ID NO: 1, a CDR2 region with at least 95% sequence homology to SEQ ID NO: 2 and a CDR3 region with at least 95% sequence homology to SEQ ID NO: 3; and a light chain variable region having a CDR1 region with at least 95% sequence homology to SEQ ID NO: 4, a CDR2 region with at least 95% sequence homology to SEQ ID NO: 5 and a CDR3 region with at least 95% sequence homology to SEQ ID NO: 6.

2. The method according to claim 1 , wherein the monoclonal antibody comprises a heavy chain variable region having a CDR1 region as shown in SEQ ID NO: 1, a CDR2 region as shown in SEQ ID NO: 2 and a CDR3 region as shown in SEQ ID NO: 3; and a light chain variable region having a CDR1 region as shown in SEQ ID NO: 4, a CDR2 region as shown in SEQ ID NO: 5 and a CDR3 region as shown in SEQ ID NO: 6.

3. The method according to claim 1 , wherein the heavy chain variable region of the monoclonal antibody has an amino acid sequence as shown in SEQ ID NO: 7; and the light chain variable region of the monoclonal antibody has an amino acid sequence as shown in SEQ ID NO: 8.

4. The method according to claim 3 , wherein the heavy chain variable region of the monoclonal antibody is encoded by a nucleotide sequence as shown in SEQ ID NO: 11; or the light chain variable region of the monoclonal antibody is encoded by a nucleotide sequence as shown in SEQ ID NO: 12.

5. The method according to claim 1 , wherein the heavy chain of the monoclonal antibody has an amino acid sequence as shown in SEQ ID NO: 9; or the light chain of the monoclonal antibody has an amino acid sequence as shown in SEQ ID NO: 10.

6. The method according to claim 5 , wherein the heavy chain of the monoclonal antibody is encoded by a nucleotide sequence as shown in SEQ ID NO: 13; or the light chain of the monoclonal antibody is encoded by a nucleotide sequence as shown in SEQ ID NO: 14.

7. The method according to claim 1 , wherein the binding molecule is administered to the subject at an amount in the range of 0.1-100 mg/kg body weight.

8. A method for inhibiting IL-1, IL-6, or IL-17 production, comprising administering to a subject in need thereof a binding molecule which specifically binds to a precursor of brain-derived neurotrophic factor, wherein the binding molecule is a monoclonal antibody comprising a heavy chain variable region having a CDR1 region with at least 95% sequence homology to SEQ ID NO: 1, a CDR2 region with at least 95% sequence homology to SEQ ID NO: 2 and a CDR3 region with at least 95% sequence homology to SEQ ID NO: 3; and a light chain variable region having a CDR1 region with at least 95% sequence homology to SEQ ID NO: 4, a CDR2 region with at least 95% sequence homology to SEQ ID NO: 5 and a CDR3 region with at least 95% sequence homology to SEQ ID NO: 6.

9. The method according to claim 8 , wherein the monoclonal antibody comprising a heavy chain variable region having a CDR1 region as shown in SEQ ID NO: 1, a CDR2 region as shown in SEQ ID NO: 2 and a CDR3 region as shown in SEQ ID NO: 3; and a light chain variable region having a CDR1 region as shown in SEQ ID NO: 4, a CDR2 region as shown in SEQ ID NO: 5 and a CDR3 region as shown in SEQ ID NO: 6.

10. The method according to claim 8 , wherein the heavy chain variable region of the monoclonal antibody has an amino acid sequence as shown in SEQ ID NO: 7; and the light chain variable region of the monoclonal antibody has an amino acid sequence as shown in SEQ ID NO: 8.

11. The method according to claim 10 , wherein the heavy chain of the monoclonal antibody has an amino acid sequence as shown in SEQ ID NO: 9; or the light chain of the monoclonal antibody has an amino acid sequence as shown in SEQ ID NO: 10.

12. The method according to claim 8 , wherein the binding molecule is administered to the subject at an amount in the range of 0.1-100 mg/kg body weight.

13. A method for inhibiting interferon gamma (IFN-γ) or tumor necrosis factor alpha (TNF-α) production, comprising administering to a subject in need thereof a binding molecule which specifically binds to a precursor of brain-derived neurotrophic factor, wherein the binding molecule is a monoclonal antibody comprising a heavy chain variable region having a CDR1 region with at least 95% sequence homology to SEQ ID NO: 1, a CDR2 region with at least 95% sequence homology to SEQ ID NO: 2 and a CDR3 region with at least 95% sequence homology to SEQ ID NO: 3; and a light chain variable region having a CDR1 region with at least 95% sequence homology to SEQ ID NO: 4, a CDR2 region with at least 95% sequence homology to SEQ ID NO: 5 and a CDR3 region with at least 95% sequence homology to SEQ ID NO: 6.

14. The method according to claim 13 , wherein the monoclonal antibody comprising a heavy chain variable region having a CDR1 region as shown in SEQ ID NO: 1, a CDR2 region as shown in SEQ ID NO: 2 and a CDR3 region as shown in SEQ ID NO: 3; and a light chain variable region having a CDR1 region as shown in SEQ ID NO: 4, a CDR2 region as shown in SEQ ID NO: 5 and a CDR3 region as shown in SEQ ID NO: 6.

15. The method according to claim 13 , wherein the heavy chain variable region of the monoclonal antibody has an amino acid sequence as shown in SEQ ID NO: 7; and the light chain variable region of the monoclonal antibody has an amino acid sequence as shown in SEQ ID NO: 8.

16. The method according to claim 13 , wherein the heavy chain of the monoclonal antibody has an amino acid sequence as shown in SEQ ID NO: 9; or the light chain of the monoclonal antibody has an amino acid sequence as shown in SEQ ID NO: 10.

17. The method according to claim 13 , wherein the binding molecule is administered to the subject at an amount in the range of 0.1-100 mg/kg body weight.

Assignments (3)
CHANGE OF NAME Recorded Sep 14, 2025
From: SUZHOU AUZONE BIOLOGICAL TECHNOLOGY CO., LTD.
To: SHANGHAI AUZONE BIOLOGICAL TECHNOLOGY CO., LTD.
Reel/Frame 072246/0228 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 14, 2023
From: SHANGHAI YILE BIOTECHNOLOGY CO., LTD.
To: SUZHOU AUZONE BIOLOGICAL TECHNOLOGY CO., LTD.
Reel/Frame 065872/0881 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 21, 2017
From: LI, CHANGQI; WANG, HUAMAO; DAI, RUPING; CAI, XIUMEI; ZHOU, XINFU
To: SHANGHAI YILE BIOTECHNOLOGY CO., LTD.
Reel/Frame 043069/0706 →
Priority Claims (1)
CN 2014 1 0811678 · Dec 19, 2014 · national
Continuity (2)
Continuation In Part PCTCN2015097820 · Dec 18, 2015
Related Publication 20170362313A1 · Dec 21, 2017