IP Library Granted Patent US 9,228,185
Granted Patent B2
US 9,228,185 · App. 13/743,399 · Granted Jan 5, 2016

Modulation of BCL11A for treatment of hemoglobinopathies

Inventors: Stuart H. Orkin (Brookline, MA); Vijay G. Sankaran (Jamaica Plain, MA)
Assignees: CHILDREN'S MEDICAL CENTER CORPORATION; PRESIDENT AND FELLOWS OF HARVARD COLLEGE
C12N15/113A01K67/0275A61K31/713A61K35/28A61K49/00C07K14/4705C07K14/805C12N15/8509C12N15/86A01K2217/052A01K2217/15A01K2227/105A01K2267/0381C12N2310/14C12N2310/531C12N2740/15043C12N2800/206
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 9,228,185
App. No.
13/743,399
Granted
Jan 5, 2016
Kind
B2
Abstract

The invention relates to methods and uses of modulating fetal hemoglobin expression (HbF) in a hematopoietic progenitor cells via inhibitors of BCL11A expression or activity, such as RNAi and antibodies.

Claims (23)

1. A method of treatment of a hemoglobinopathy in a subject comprising administering an effective amount of a composition comprising an inhibitor of BCL11A, wherein the inhibitor of BCL11A is a nucleic acid that inhibits the expression of BCL11A and hybridizes to BCL11A, and whereby fetal hemoglobin expression is increased in the subject relative to prior to the administration.

2. The method of claim 1 , wherein the nucleic acid is a BCL11A specific RNA interference agent, or a vector encoding a BCL11A specific RNA interference agent.

3. The method of claim 1 , wherein the RNA interference agent comprises one or more of the nucleotide sequences of SEQ ID NO:1-6.

4. The method of claim 1 , wherein the subject has been diagnosed with a hemoglobinopathy.

5. The method of claim 1 further comprising selecting a subject who has been diagnosed with a hemoglobinopathy.

6. The method of claim 1 , wherein the hemoglobinopathy is a β-hemoglobinopathy.

7. The method of claim 1 , wherein the hemoglobinopathy is sickle cell disease.

8. The method of claim 1 , wherein the hemoglobinopathy is β-thalassemia.

9. The method of claim 1 , wherein the composition further comprising a pharmaceutically acceptable carrier or diluent.

10. The method of claim 1 , wherein the composition is administered by injection, infusion, instillation, or ingestion.

11. The method of claim 10 , wherein the composition is administered by injection, infusion, instillation, or ingestion.

12. A method of treatment of a hemoglobinopathy in a subject comprising administering an effective amount of a composition comprising hematopoietic progenitor cells to the subject, wherein the hematopoietic progenitor cells have been contacted ex vivo or in vitro with an effective amount of an inhibitor of BCL11A, wherein the inhibitor of BCL11A is a nucleic acid that inhibits the expression of BCL11A and hybridizes to BCL11A, and whereby fetal hemoglobin expression is increased in the subject relative to prior to the administration.

13. The method of claim 12 , wherein the nucleic acid is a BCL11A specific RNA interference agent, or a vector encoding a BCL11A specific RNA interference agent.

14. The method of claim 12 , wherein the RNA interference agent comprises one or more of the nucleotide sequences of SEQ ID NOS:1-6.

15. The method of claim 12 , wherein the subject has been diagnosed with a hemoglobinopathy.

16. The method of claim 12 further comprising selecting a subject who has been diagnosed with a hemoglobinopathy.

17. The method of claim 12 , wherein the hemoglobinopathy is a β-hemoglobinopathy.

18. The method of claim 12 , wherein the hemoglobinopathy is sickle cell disease.

19. The method of claim 12 , wherein the hemoglobinopathy is β-thalassemia.

20. The method of claim 12 , wherein the hematopoietic progenitor cells are derived from the subject.

21. The method of claim 12 , wherein the hematopoietic progenitor cells are expanded in vitro prior to administering to the subject.

22. The method of claim 12 , wherein the composition further comprising a pharmaceutically acceptable carrier or diluent.

23. The method of claim 12 , wherein the composition is administered by injection or infusion.

Assignments (4)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 28, 2018
From: ORKIN, STUART H.
To: HOWARD HUGHES MEDICAL INSTITUTE
Reel/Frame 046726/0253 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 28, 2018
From: SANKARAN, VIJAY G.
To: CHILDREN'S MEDICAL CENTER CORPORATION
Reel/Frame 046726/0309 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 29, 2015
From: HOWARD HUGHES MEDICAL INSTITUTE
To: CHILDREN'S MEDICAL CENTER CORPORATION
Reel/Frame 035927/0479 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 29, 2015
From: CHILDREN'S MEDICAL CENTER CORPORATION
To: PRESIDENT AND FELLOWS OF HARVARD COLLEGE
Reel/Frame 035927/0485 →
Continuity (4)
Continuation 13063524
Provisional Application 61097017 · Sep 15, 2008
Provisional Application 61222571 · Jul 2, 2009
Related Publication 20130129629A1 · May 23, 2013