IP Library › Granted Patent US 11,104,728
Granted Patent B2
US 11,104,728 · App. 16/497,612 · Granted Aug 31, 2021

Anti-EMAP II antibody and use thereof

Inventors: Sang Gyu Park (Gyeonggi-do, KR); Gook-Jin Kang (Seoul, KR)
Assignee: HUB Biotech Co., Ltd.
C07K16/24A61P19/02G01N33/6854A61K2039/505C07K2317/24C07K2317/52C07K2317/565G01N2800/2821
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Quick Facts
Patent No.
US 11,104,728
App. No.
16/497,612
Granted
Aug 31, 2021
Kind
B2
Abstract

The present invention relates to an anti-EMAP II antibody or an antigen-binding fragment thereof, a nucleic acid molecule for coding the same, or a preparation method thereof. Also, the present invention provides a method for using the anti-EMAP II antibody or the antigen-binding fragment thereof in preventing, treating or diagnosing EMAP II-mediated diseases, for example, TNF-α-mediated disease or Alzheimer's disease. Furthermore, the present invention provides a method for using the anti-EMAP II antibody or the antigen-binding fragment thereof in detecting or quantifying an EMAP II antigen. The antibody of the present invention may exhibit a more improved antigen-binding capacity compared to existing anti-EMAP antibodies and may treat the TNF-α-mediated disease more effectively.

Claims (14)

1. An anti-EMAP II (endothelial monocyte activating polypeptide II) antibody or an antigen-binding fragment thereof, comprising a light chain variable region, containing a light chain CDR1 consisting of SEQ ID NO: 7, a light chain CDR2 consisting of SEQ ID NO: 9, and a light chain CDR3 consisting of SEQ ID NO: 11; and a heavy chain variable region, containing a heavy chain CDR1 consisting of SEQ ID NO: 12, a heavy chain CDR2 consisting of SEQ ID NO: 14, and a heavy chain CDR3 consisting of SEQ ID NO: 16.

2. The anti-EMAP II antibody or the antigen-binding fragment thereof according to claim 1 , wherein the antibody comprises a light chain variable region consisting of SEQ ID NO: 3; and a heavy chain variable region consisting of SEQ ID NO: 4.

3. The anti-EMAP II antibody or the antigen-binding fragment thereof according to claim 1 , characterized in that the antibody is a humanized antibody.

4. The anti-EMAP II antibody or the antigen-binding fragment thereof according to claim 1 , wherein the antibody comprises a kappa or human IgG-derived constant region.

5. The anti-EMAP II antibody or the antigen-binding fragment thereof according to claim 1 , characterized in that the antigen binding fragment is Fab, F(ab′), F(ab′)2 or Fv.

6. A nucleic acid molecule for coding the antibody or the antigen-binding fragment thereof according to claim 1 .

7. A recombinant vector comprising the nucleic acid molecule according to claim 6 .

8. A transformed cell comprising the recombinant vector according to claim 7 .

9. A method for preparing an anti-EMAP II antibody or an antigen-binding fragment thereof, comprising a step of expressing the anti-EMAP II antibody or the antigen-binding fragment thereof by culturing the transformed cell according to claim 8 and (ii) a step of isolating the anti-EMAP II antibody or the antigen-binding fragment thereof.

10. A pharmaceutical composition, comprising the anti-EMAP II antibody or the antigen-binding fragment thereof according to claim 1 as an active ingredient.

11. A composition for detecting an EMAP II antigen, comprising the anti-EMAP II antibody or the antigen-binding fragment thereof according to claim 1 as an active ingredient.

12. A kit for detecting an EMAP II antigen, comprising the anti-EMAP II antibody or the antigen-binding fragment thereof according to claim 1 as an active ingredient.

13. A method for detecting an EMAP II antigen in a sample, comprising a step of bringing the anti-EMAP II antibody or the antigen-binding fragment thereof according to claim 1 into contact with the sample.

14. A method for treating EMAP II-mediated disease, including administering a therapeutically effective amount of a composition comprising the anti-EMAP II antibody or the antigen binding fragment thereof according to claim 1 , wherein the EMAP II-mediated disease is rheumatoid arthritis.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 6, 2021
From: L&K BIOMED CO., LTD.
To: HUB BIOTECH CO., LTD.
Reel/Frame 056161/0426 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 11, 2019
From: PARK, SANG GYU; KANG, GOOK-JIN
To: L&K BIOMED CO., LTD.
Reel/Frame 050987/0802 →
Priority Claims (1)
KR 10-2017-0038706 · Mar 27, 2017 · national
Continuity (1)
Related Publication 20200040071A1 · Feb 6, 2020