IP Library Granted Patent US 8,603,476
Granted Patent B2
US 8,603,476 · App. 12/812,341 · Granted Dec 10, 2013

Humanized anti-human α9-integrin antibody

Inventors: Kenji Uehara (Kikuchi, JP); Hirofumi Higuchi (Kikuchi, JP); Toshihiro Nakashima (Kikuchi, JP); Daisuke Ishikawa (Kikuchi, JP); Nobuchika Yamamoto (Tokyo, JP); Hirotada Fujita (Tokyo, JP); Fumihiko Sakai (Tokyo, JP)
Assignee: Astellas Pharma Inc.
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Quick Facts
Patent No.
US 8,603,476
App. No.
12/812,341
Granted
Dec 10, 2013
Kind
B2
Abstract

The present invention provides a humanized anti-human α9 integrin antibody having improved activity and/or property as compared to a donor mouse anti-human α9 integrin antibody, namely, a humanized anti-human α9 integrin antibody containing a heavy-chain variable region consisting of the amino acid sequence shown by SEQ ID NO:11 and a light-chain variable region consisting of the amino acid sequence shown by SEQ ID NO:17, a humanized anti-human α9 integrin antibody containing a heavy-chain variable region consisting of the amino acid sequence shown by SEQ ID NO:13 and a light-chain variable region consisting of the amino acid sequence shown by SEQ ID NO:17, a humanized anti-human α9 integrin antibody containing a heavy-chain variable region consisting of the amino acid sequence shown by SEQ ID NO:15 and a light-chain variable region consisting of the amino acid sequence shown by SEQ ID NO:9, and a means for the prophylaxis or treatment of various diseases involving human α9 integrin in the pathogenesis, which uses the antibody.

Claims (14)

1. A humanized anti-human α9 integrin antibody comprising a heavy-chain variable region consisting of the amino acid sequence shown by SEQ ID NO:11 and a light-chain variable region consisting of the amino acid sequence shown by SEQ ID NO:17.

2. The humanized anti-human α9 integrin antibody according to claim 1 , wherein the heavy-chain constant region of the antibody is human Igγ1.

3. The humanized anti-human α9 integrin antibody according to claim 1 , wherein the light-chain constant region of the antibody is human Igκ.

4. The humanized anti-human α9 integrin antibody according to claim 1 , wherein the heavy-chain constant region of the antibody is human Igγ1 and the light-chain constant region of the antibody is human Igκ.

5. The humanized anti-human α9 integrin antibody according to claim 1 , wherein the heavy chain consists of the amino acid sequence shown by SEQ ID NO:19 and the light-chain consists of the amino acid sequence shown by SEQ ID NO:25.

6. A polynucleotide comprising a sequence encoding the heavy-chain variable region of the humanized anti-human α9 integrin antibody according to claim 1 .

7. A polynucleotide comprising a sequence encoding the light-chain variable region of the humanized anti-human α9 integrin antibody according to claim 1 .

8. An expression vector comprising a polynucleotide comprising a sequence encoding the heavy-chain variable region of the humanized anti-human α9 integrin antibody according to claim 1 and/or a polynucleotide comprising a sequence encoding the light-chain variable region of the humanized anti-human α9 integrin antibody according to claim 1 .

9. A host cell incorporating the expression vector according to claim 8 .

10. A method of producing a humanized anti-human α9 integrin antibody according to claim 1 , comprising a step of culturing a host cell to allow expression of the humanized anti-human α9 integrin antibody, wherein the host cell incorporates an expression vector comprising a polynucleotide comprising a sequence encoding the heavy-chain variable region of the humanized anti-human α9 integrin antibody and a polynucleotide comprising a sequence encoding the light-chain variable region of the humanized anti-human α9 integrin antibody.

11. A method of treating rheumatoid arthritis, comprising administering a therapeutically effective amount of the humanized anti-human α9 integrin antibody according to claim 1 .

12. A pharmaceutical for treating rheumatoid arthritis comprising the humanized anti-human α9 integrin antibody according to claim 1 .

13. A pharmaceutical composition comprising the humanized anti-human α9 integrin antibody according to claim 1 and a pharmaceutically acceptable carrier.

14. The pharmaceutical composition according to claim 13 , which is in the form of an injection or drip infusion.

Assignments (3)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 24, 2013
From: THE CHEMO-SERO-THERAPEUTIC RESEARCH INSTITUTE
To: ASTELLAS PHARMA INC.
Reel/Frame 031466/0555 →
CHANGE OF NAME Recorded Oct 24, 2013
From: JURIDICAL FOUNDATION THE CHEMO-SERO-THERAPEUTIC RESEARCH INSTITUTE
To: THE CHEMO-SERO-THERAPEUTIC RESEARCH INSTITUTE
Reel/Frame 031485/0329 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 19, 2010
From: UEHARA, KENJI; HIGUCHI, HIROFUMI; NAKASHIMA, TOSHIHIRO; ISHIKAWA, DAISUKE; YAMAMOTO, NOBUCHIKA; FUJITA, HIROTADA; SAKAI, FUMIHIKO
To: JURIDICAL FOUNDATION THE CHEMO-SERO-THERAPEUTIC RESEARCH INSTITUTE; ASTELLAS PHARMA INC.
Reel/Frame 025377/0436 →
Priority Claims (2)
JP 2008-004975 · Jan 11, 2008 · national
JP 2008-282496 · Oct 31, 2008 · national
Continuity (1)
Related Publication 20110059077A1 · Mar 10, 2011