IP Library Granted Patent US 7,265,083
Granted Patent B2
US 7,265,083 · App. 10/104,755 · Granted Sep 4, 2007

Treatment of idiopathic pulmonary fibrosis using IP-10

Assignee: The Regents of The University of Michigan
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Quick Facts
Patent No.
US 7,265,083
App. No.
10/104,755
Granted
Sep 4, 2007
Kind
B2
Abstract

Disclosed are various discoveries concerning the angiogenic and angiostatic properties of the CXC chemokines, including the finding that the ELR motif controls the ability of these molecules to induce angiogenesis. Aspects of the invention include, for example, the identification of IP-10, MIG and certain IL-8 analogues as angiostatic agents, and their use in inhibiting angiogenesis in various systems.

Claims (11)

1. A method of treating idiopathic pulmonary fibrosis, comprising administering to an animal with idiopathic pulmonary fibrosis a pharmaceutically acceptable composition that comprises a therapeutically effective amount of IP-10 (γ-interferon-inducible protein-10).

2. The method of claim 1 , wherein said pharmaceutically acceptable composition comprises IP-10 prepared by expressing an IP-10 nucleic acid in a recombinant host cell and collecting the expressed IP-10 protein.

3. The method of claim 1 , wherein said pharmaceutically acceptable composition comprises IP-10 prepared by automated peptide synthesis.

4. The method of claim 1 , wherein said pharmaceutically acceptable composition is administered to said animal parenterally.

5. The method of claim 1 , wherein said pharmaceutically acceptable composition is administered to said animal by direct instillation into the disease site.

6. The method of claim 1 , wherein said animal is a human subject.

7. The method of claim 6 , wherein said pharmaceutically acceptable composition comprises a native human IP-10 polypeptide.

8. The method of claim 6 , wherein said pharmaceutically acceptable composition comprises an IP-10 polypeptide that comprises the amino acid sequence of SEQ ID NO:1.

9. The method of claim 8 , wherein said pharmaceutically acceptable composition comprises an IP-10 polypeptide that consists of the amino acid sequence of SEQ ID NO:1.

10. The method of claim 6 , wherein said pharmaceutically acceptable composition comprises an IP-10 polypeptide that comprises a variant of the amino acid sequence of SEQ ID NO:1, wherein the variant inhibits angiogenesis.

11. A method for treating idiopathic pulmonary fibrosis, comprising administering to an animal with idiopathic pulmonary fibrosis a pharmaceutically acceptable composition that comprises an amount of IP-10 effective to inhibit angiogenesis associated with idiopathic pulmonary fibrosis.

Assignments (2)
CONFIRMATORY LICENSE Recorded Feb 9, 2019
From: UNIVERSITY OF MICHIGAN
To: NATIONAL INSTITUTES OF HEALTH-DIRECTOR DEITR
Reel/Frame 048286/0493 →
CONFIRMATORY LICENSE Recorded Oct 13, 2016
From: UNIVERSITY OF MICHIGAN
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 040337/0961 →
Continuity (3)
Continuation 0921338300 · Dec 9, 1998
Division 0846881900 · Jun 6, 1995
Related Publication 20030031645A1 · Feb 13, 2003