IP Library Granted Patent US 8,017,119
Granted Patent B2
US 8,017,119 · App. 12/147,331 · Granted Sep 13, 2011

Antibody against periostin, and a pharmaceutical composition comprising it for preventing or treating a disease in which periostin is involved

View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 8,017,119
App. No.
12/147,331
Granted
Sep 13, 2011
Kind
B2
Abstract

The present invention provides an antibody against a periostin isoform having anti-cell adhesive activity, especially an anti-periostin antibody having the ability to neutralize anti-cell adhesive properties, as well as a prophylactic or therapeutic agent for periostin-related diseases comprising the antibody. The present invention also provides methods for detecting and quantifying the periostin isoform in a sample by using the antibody, as well as a method for diagnosing periostin-related diseases comprising measuring the amount of the periostin isoform by the detection or quantification method.

Claims (27)

1. A method for treating heart failure, myocardial infarction, or cancer, comprising administering to a patient an antibody against a periostin isoform having anti-cell adhesive activity, that specifically recognizes the amino acid sequence encoded by Exon-17 or a part thereof, and is capable of neutralizing anti-cell adhesive activity of periostin.

2. The method of claim 1 , wherein the disease is cancer.

3. The method of claim 2 , wherein the disease is cancer of breast, large intestine, lung, malignant melanoma, bone, pancreas, stomach, skin, uterus, ovary, rectum, colon, esophagus, small intestine, thyroid, adrenal gland, prostrate, bladder or kidney.

4. The method of claim 2 , wherein cancer is treated by inhibiting cancer metastasis.

5. The method of claim 2 , wherein cancer is treated by inhibiting the growth of primary tumor.

6. The method of claim 2 , wherein cancer is treated by inhibiting the bone invasion of cancer or bone destruction caused by bone invasion of cancer.

7. The method of claim 2 , wherein the cancer is malignant melanoma or breast cancer.

8. The method of claim 1 , wherein the amino acid sequence encoded by Exon-17 or part thereof is the amino acid sequence of SEQ ID NO: 3, 4, 21, 22, 23, 24, 26 or 34.

9. The method of claim 8 , wherein the amino acid sequence is the amino acid sequence of SEQ ID NO: 3, 4, or 21.

10. The method of any one of claims 1 , 8 , or 9 , wherein the antibody is a monoclonal antibody.

11. The method of claim 10 , further comprising producing the monoclonal antibody using a hydridoma cell line FERM BP-10718.

12. The method of claim 10 , further comprising producing the monoclonal antibody by the method comprising:

immunizing a mammal with a peptide having the amino acid sequence of SEQ ID NO: 3, 4, or 21, or a peptide thereof comprising cysteine residues introduced into the N-terminus thereof;

fusing an antibody-producing cell of the mammal with a myeloma cell; and

culturing the obtained hybridoma.

13. The method of claim 3 , further comprising treating cancer by inhibiting cancer metastasis.

14. The method of claim 3 , further comprising treating cancer by inhibiting the growth of primary tumor.

15. The method of claim 3 , further comprising treating cancer by inhibiting the bone invasion of cancer or bone destruction caused by bone invasion of cancer.

16. The method of claim 3 , wherein the cancer is malignant melanoma or breast cancer.

17. The method of claim 4 , wherein the cancer is malignant melanoma or breast cancer.

18. The method of claim 5 , wherein the cancer is malignant melanoma or breast cancer.

19. The method of claim 6 , wherein the cancer is malignant melanoma or breast cancer.

20. The method of claim 1 , wherein the disease is heart failure.

21. The method of claim 1 , wherein the disease is myocardial infarction.

22. The method of claim 1 , wherein the disease is lung metastasis of breast cancer.

23. A method for neutralizing anti-cell adhesive activity of periostin comprising binding an antibody that specifically recognizes the amino acid sequence encoded by Exon-17 or a part thereof, and is capable of neutralizing anti-cell adhesive activity of periostin.

24. The method of claim 23 , wherein the amino acid sequence encoded by Exon-17 or a part thereof is produced in a cancer cell.

Assignments (5)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 1, 2013
From: DAIICHI SANKYO COMPANY, LIMITED
To: OSAKA UNIVERSITY
Reel/Frame 030120/0931 →
CHANGE OF NAME Recorded Jul 7, 2010
From: ASUBIO PHARMA CO., LTD.
To: DAIICHI SANKYO COMPANY, LIMITED
Reel/Frame 024643/0791 →
CORRECTIVE ASSIGNMENT TO CORRECT THE OSAKA UNIVERSITY'S ADDRESS PREVIOUSLY RECORDED ON REEL 021979 FRAME 0503. ASSIGNOR(S) HEREBY CONFIRMS THE THAT 1-1, YAMADAOKA, SUITA-SHI, OSAKA 565-0871 JAPAN IS THE CORRECT ADDRESS. Recorded Feb 20, 2009
From: TANIYAMA, YOSHIAKI; MORISHITA, RYUICHI; KATSURAGI, NARUTO
To: ASUBIO PHARMA CO., LTD.; OSAKA UNIVERSITY
Reel/Frame 022286/0429 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 15, 2008
From: TANIYAMA, YOSHIAKI; MORISHITA, RYUICHI; KATSURAGI, NARUTO
To: ASUBIO PHARMA CO., LTD.; OSAKA UNIVERSITY
Reel/Frame 021979/0503 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 11, 2008
From: TANIYAMA, YOSHIAKI; MORISHITA, RYUICHI; KATSURAGI, NARUTO
To: ASUBIO PHARMA CO., LTD.; OSAKA UNIVERSITY
Reel/Frame 021512/0435 →