IP Library Granted Patent US 8,217,020
Granted Patent B2
US 8,217,020 · App. 12/950,672 · Granted Jul 10, 2012

Methods and compositions for reducing viral genome amounts in a target cell

Assignee: The Board of Trustees of the Leland Stanford Junior University
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Quick Facts
Patent No.
US 8,217,020
App. No.
12/950,672
Granted
Jul 10, 2012
Kind
B2
Abstract

Methods and compositions for reducing viral genome amounts in a target cell are provided. In the subject methods, the activity of a miRNA is inhibited in a manner sufficient to reduce the amount of viral genome in the target cell, e.g., by introducing a miRNA inhibitory agent in the target cell. Also provided are pharmaceutical compositions, kits and systems for use in practicing the subject methods. The subject invention finds use in a variety of applications, including the treatment of subjects suffering from a viral mediated disease condition, e.g., an HCV mediated disease condition.

Claims (22)

1. A method of treating a subject infected with Hepatitis C (HCV) virus comprising: administering to said subject an miRNA inhibitory agent targeted to miR-122, wherein said miRNA inhibitory agent comprises an antisense oligonucleotide complementary to said miR-122.

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

3. The method of claim 1 , wherein said subject is a mammal.

4. The method of claim 1 , wherein said antisense oligonucleotide is completely complementary to said miR-122.

5. The method of claim 1 , wherein said antisense oligonucleotide comprises the nucleotide sequence of SEQ ID NO:18.

6. The method of claim 1 , wherein said antisense oligonucleotide comprises the nucleotide sequence of SEQ ID NO:15.

7. The method of claim 1 , wherein said subject is infected with HCV-1a.

8. The method of claim 1 , wherein said subject is infected with HCV-1b.

9. The method of claim 1 , wherein said subject is infected with HCV-2.

10. The method of claim 1 , wherein said subject is infected with HCV-3.

11. The method of claim 1 , wherein said subject is infected with HCV-4.

12. The method of claim 1 , wherein said subject is infected with HCV-5.

13. The method of claim 1 , wherein said subject is infected with HCV-6.

14. The method of claim 1 , further comprising administering at least one additional agent selected from the group consisting of an antiviral agent and an interferon.

15. The method of claim 14 , wherein said at least one additional agent comprises an antiviral agent.

16. The method of claim 14 , wherein said at least one additional agent comprises an interferon.

17. The method of claim 16 , wherein said interferon comprises interferon alfa-2b.

18. The method of claim 16 , wherein said interferon comprises interferon alfa-2a.

19. The method of claim 16 , wherein said interferon comprises interferon alfacon-1.

20. The method of claim 16 , wherein the interferon comprises a pegylated interferon.

21. The method of claim 14 , wherein said antiviral agent comprises ribavirin.

22. The method of claim 1 , wherein said antisense oligonucleotide comprises a 2′-O-methyl modification.

Assignments (2)
CONFIRMATORY LICENSE Recorded Aug 29, 2011
From: THE BOARD OF TRUSTEES OF THE LELAND STANFORD JUNIOR UNIVERSITY
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 026819/0553 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 7, 2011
From: SARNOW, PETER; JOPLING, CATHERINE L.; LANCASTER, ALISSA M.
To: THE BOARD OF TRUSTEES OF THE LELAND STANFORD JUNIOR UNIVERSITY
Reel/Frame 025911/0390 →
Continuity (4)
Continuation 11953705 · Dec 10, 2007
Continuation 11122328 · May 3, 2005
Provisional Application 60568358 · May 4, 2004
Related Publication 20110124707A1 · May 26, 2011