IP Library Granted Patent US 9,260,755
Granted Patent B2
US 9,260,755 · App. 13/861,227 · Granted Feb 16, 2016

Compositions and methods for characterizing and treating muscular dystrophy

Inventors: Charles P. Emerson, Jr. (Lyndon, MA); Jennifer Chen (Watertown, MA); Oliver D. King (Cambridge, MA)
Assignee: University of Massachusetts
C12Q1/6883A01K67/0271C12N5/0658C12N15/111C12N15/113C12N2310/11C12N2310/315C12N2310/322C12N2310/3233C12N2310/341C12N2310/346C12N2320/12C12Q2600/106C12Q2600/158
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Quick Facts
Patent No.
US 9,260,755
App. No.
13/861,227
Granted
Feb 16, 2016
Kind
B2
Abstract

Compositions and methods for identifying new treatments for Facioscapulohumeral muscular dystrophy (FSHD), and uses thereof.

Claims (16)

1. A chimeric mouse comprising human cells derived from an FSHD affected subject or a first degree relative thereof, wherein the human cells replace 25-50% or more of the cells present in a skeletal muscle of the mouse.

2. The mouse of claim 1 , wherein the human cells replace cells present in the tibialis anterior.

3. A set of chimeric mice comprising one mouse comprising human cells derived from an FSHD affected subject, wherein the human cells replace 25-50% or more of the cells present in a skeletal muscle of the mouse, and at least one mouse comprising human cells derived from a first degree relative of the FSHD affected subject, wherein the human cells replace 25-50% or more of the cells present in a skeletal muscle of the mouse.

4. A method of identifying an agent that ameliorates FSHD in a subject in need thereof, the method comprising administering the agent to the chimeric mouse of claim 1 , and comparing the level of expression of a nucleic acid molecule of Table 2 or 4 in a human cell of the mouse relative to the level in an untreated control cell, wherein an agent that normalizes expression in said cell is identified as ameliorating FSHD.

5. The mouse of claim 1 , wherein the human cells are enriched for myogenic cells.

6. The mouse of claim 1 , wherein the human cells are isolated by selecting for cells positive for human CD 56.

7. The mouse of claim 1 , wherein the human cells are skeletal muscle cells, muscle stem cells, or differentiated muscle fiber.

8. The mouse of claim 1 , wherein the human cells are obtained from skeletal muscle biopsies.

9. The mouse of claim 8 , wherein the biopsy is of a bicep or deltoid muscle.

10. The method of claim 4 , wherein the nucleic acid molecule is selected from the group consisting of PRAMEF1, TRIM43, SLC34A2, TRIM49, TC2N, CD34, NAAA, HSPA6, and CD177.

11. A chimeric mouse created by a method comprising injecting a skeletal muscle of a mouse with at least or about 1×10 6 human FSHD myoblasts derived from an FSHD affected subject or a first degree relative thereof.

12. The chimeric mouse of claim 11 , wherein the myoblasts are derived from skeletal muscle.

13. The chimeric mouse of claim 11 , wherein the myoblasts are derived from a bicep or deltoid muscle.

14. A chimeric mouse comprising an engraftment in a skeletal muscle of at least or about 100,000 human nuclei derived from an FSHD affected subject or a first degree relative thereof.

15. The chimeric mouse of claim 14 , wherein the nuclei are derived from skeletal muscle.

16. The chimeric mouse of claim 14 , wherein the nuclei are derived from a bicep or deltoid muscle.

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 042265/0814 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 22, 2013
From: EMERSON, CHARLES P., JR.; CHEN, JENNIFER; KING, OLIVER D.
To: UNIVERSITY OF MASSACHUSETTS
Reel/Frame 031449/0057 →
Continuity (2)
Provisional Application 61622942 · Apr 11, 2012
Related Publication 20130347136A1 · Dec 26, 2013