IP Library › Granted Patent US 11,198,730
Granted Patent B2
US 11,198,730 · App. 16/325,150 · Granted Dec 14, 2021

Anti-LAG-3 antibody

Inventors: Satoru Konnai (Hokkaido, JP); Kazuhiko Ohashi (Hokkaido, JP); Shiro Murata (Hokkaido, JP); Tomohiro Okagawa (Hokkaido, JP); Asami Nishimori (Hokkaido, JP); Naoya Maekawa (Hokkaido, JP); Yasuhiko Suzuki (Hokkaido, JP); Chie Nakajima (Hokkaido, JP)
Assignees: Fuso Pharmaceutical Industries, Ltd.; National University Corporation Hokkaido University
C07K16/2803A61K39/395A61P15/14A61P31/00A61P31/04A61P31/06A61P31/10A61P33/02A61P35/00A61P35/02C07K16/28C07K16/46C12N5/10C12N15/09C12N15/85C12N2015/8518
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Quick Facts
Patent No.
US 11,198,730
App. No.
16/325,150
Granted
Dec 14, 2021
Kind
B2
Abstract

The present invention provides an anti-LAG-3 antibody capable of repeated administration even to animals other than rat. An anti-LAG-3 antibody comprising (a) a light chain comprising a light chain variable region containing CDR1 having the amino acid sequence of QSLLDSDGNTY (SEQ ID NO: 16), CDR2 having the amino acid sequence of SVS and CDR3 having the amino acid sequence of MQATHVPFT (SEQ ID NO: 17) and the light chain constant region of an antibody of an animal other than rat; and (b) a heavy chain comprising a heavy chain variable region containing CDR1 having the amino acid sequence of GFDFDTYP (SEQ ID NO: 18), CDR2 having the amino acid sequence of ITIKTHNYAT (SEQ ID NO: 19) and CDR3 having the amino acid sequence of NREDFDY (SEQ ID NO: 20) and the heavy chain constant region of an antibody of an animal other than rat. A pharmaceutical composition comprising the above anti-LAG-3 antibody as an active ingredient. A method for preparing the above anti-LAG-3 antibody is also provided.

Claims (12)

1. An anti-LAG-3 antibody comprising (a) a light chain comprising a light chain variable region containing CDR1 having the amino acid sequence of QSLLDSDGNTY (SEQ ID NO: 16), CDR2 having the amino acid sequence of SVS and CDR3 having the amino acid sequence of MQATHVPFT (SEQ ID NO: 17) and the light chain constant region of an antibody of bovine; and (b) a heavy chain comprising a heavy chain variable region containing CDR1 having the amino acid sequence of GFDFDTYP (SEQ ID NO: 18), CDR2 having the amino acid sequence of ITIKTHNYAT (SEQ ID NO: 19) and CDR3 having the amino acid sequence of NREDFDY (SEQ ID NO: 20) and the heavy chain constant region of an antibody of bovine, wherein the light chain constant region of the bovine antibody has the amino acid sequence as shown in SEO ID NO: 3 and the heavy chain constant region of the bovine antibody has the amino acid sequence as shown in SEO ID NO: 4.

2. The antibody of claim 1 , wherein the light chain variable region and the heavy chain variable region are derived from rat.

3. The antibody of claim 2 , wherein the light chain variable region is the light chain variable region of a rat anti-bovine LAG-3 antibody and the heavy chain variable region is the heavy chain variable region of a rat anti-bovine LAG-3 antibody.

4. The antibody of claim 3 , wherein the light chain variable region has the amino acid sequence as shown in SEQ ID NO. 1 and the heavy chain variable region has the amino acid sequence as shown in SEQ ID NO: 2.

5. The antibody of claim 1 which has a four-chain structure comprising two light chains and two heavy chains.

6. A pharmaceutical composition comprising the antibody of claim 1 as an active ingredient.

7. A method to treat cancer and/or infection in cattle, buffalo or sheep comprising administering an effective amount of the pharmaceutical composition of claim 6 to cattle, buffalo or sheep in need thereof so as to treat said cancer and/or infection.

8. The method of claim 7 , wherein the cancer and/or infection is selected from the group consisting of neoplastic diseases, leukemia, Johne's disease, anaplasmosis, bacterial mastitis, mycotic mastitis, mycoplasma infections, tuberculosis, Theileria orientalis infection, cryptosporidiosis, coccidiosis, trypanosomiasis and leishmaniasis.

9. An artificial genetic DNA encoding the antibody of claim 1 .

10. A vector comprising the artificial genetic DNA of claim 9 .

11. A host cell transformed with the vector of claim 10 .

12. A method of preparing an antibody, comprising culturing the host cell of claim 11 and collecting an anti-LAG-3 antibody from the resultant culture.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 19, 2019
From: NATIONAL UNIVERSITY CORPORATION HOKKAIDO UNIVERSITY
To: NATIONAL UNIVERSITY CORPORATION HOKKAIDO UNIVERSITY; FUSO PHARMACEUTICAL INDUSTRIES, LTD.
Reel/Frame 049807/0339 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 29, 2019
From: KONNAI, SATORU; OHASHI, KAZUHIKO; MURATA, SHIRO; OKAGAWA, TOMOHIRO; NISHIMORI, ASAMI; MAEKAWA, NAOYA; SUZUKI, YASUHIKO; NAKAJIMA, CHIE
To: NATIONAL UNIVERSITY CORPORATION HOKKAIDO UNIVERSITY
Reel/Frame 049304/0556 →
Priority Claims (1)
JP JP2016-159091 · Aug 15, 2016 · national
Continuity (1)
Related Publication 20190169294A1 · Jun 6, 2019