IP Library Granted Patent US 9,272,053
Granted Patent B2
US 9,272,053 · App. 13/642,740 · Granted Mar 1, 2016

AAV-based treatment of cholesterol-related disorders

Inventors: Guangping Gao (Westborough, MA); Phillip D. Zamore (Northborough, MA); Jun Xie (Shrewsbury, MA)
Assignee: University of Massachusetts
A61K48/00C12N15/86C12Q1/68C12N2310/113C12N2320/32C12N2330/51C12N2750/14143
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Quick Facts
Patent No.
US 9,272,053
App. No.
13/642,740
Granted
Mar 1, 2016
Kind
B2
Abstract

The invention in some aspects relates to methods and compositions for assessing the effectiveness of miRNA inhibitors. In other aspects of the invention, methods and compositions for treating cholesterol related disorders are provided. In one aspect of the invention, miRNA inhibitors against miR-122 and rAAV-based compositions comprising the same are provided.

Claims (13)

1. A method for treating a high cholesterol-related disorder in a subject, the method comprising:

administering an effective amount of a recombinant Adeno-Associated Virus (rAAV) to the subject, wherein the rAAV comprises at least one transgene that expresses a miRNA inhibitor that inhibits the expression of miR-122 in the subject, and wherein the miRNA inhibitor comprises or consists of a sequence as set forth in SEQ ID NO: 1, SEQ ID NO: 5, SEQ ID NO: 21, or SEQ ID NO: 23.

2. The method of claim 1 , wherein the miRNA inhibitor comprises an miR-122 binding site.

3. The method of claim 1 , wherein the miR-122 binding site is flanked by two stem sequences.

4. The method of claim 1 , wherein the miR-122 binding site comprises a non-binding, central portion that is not complementary with miR-122, flanked by two portions that are complementary with miR-122.

5. The method of claim 1 , wherein the miRNA inhibitor comprises a first miR-122 binding site and a second miR-122 binding site, wherein a first stem sequence flanks the first miR-122 binding site at its 5′-end, a second stem sequence flanks the first miR-122 binding site at its 3′-end and the second miR-122 binding site at its 5′-end, and a third stem sequence flanks the second miR-122 binding site at its 3′-end.

6. The method of claim 1 , wherein the miRNA inhibitor comprises two or more miR-122 binding sites.

7. The method of claim 1 , wherein the rAAV has a capsid of the AAV9 serotype, which has a sequence as set forth in SEQ ID NO: 3.

8. The method of claim 1 , wherein the rAAV has a capsid that is a variant of the capsid of the AAV9 serotype.

9. The method of claim 8 , wherein the rAAV has a capsid of the AAV9 serotype variant, Csp-3, which has a sequence as set forth in SEQ ID NO: 4.

10. The method of claim 1 , wherein the rAAV targets liver tissue.

11. The method of claim 1 , wherein the rAAV transduces hepatocytes.

12. The method of claim 1 , wherein administering is performed intravenously.

Assignments (2)
CONFIRMATORY LICENSE Recorded Apr 17, 2017
From: UNIVERSITY OF MASSACHUSETTS MEDICAL SCH
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 042265/0816 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 18, 2015
From: GAO, GUANGPING; ZAMORE, PHILLIP D.; XIE, JUN; HOWARD HUGHES MEDICAL INSTITUTE
To: UNIVERSITY OF MASSACHUSETTS
Reel/Frame 036596/0405 →
Continuity (2)
Provisional Application 61327383 · Apr 23, 2010
Related Publication 20130101558A1 · Apr 25, 2013