IP Library Granted Patent US 12,110,499
Granted Patent B2
US 12,110,499 · App. 16/608,182 · Granted Oct 8, 2024

Homology directed repair compositions for the treatment of hemoglobinopathies

Inventors: Andrew Scharenberg (Seattle, WA); Kyle Jacoby (Seattle, WA); Hans-Peter Kiem (Seattle, WA); David J. Rawlings (Seattle, WA); Christopher Lux (Bremerton, WA); Sowmya Pattabhi (Bellevue, WA); Olivier M. Humbert (Seattle, WA)
Assignee: Seattle Children's Hospital
C12N15/907A61K35/28A61P9/00C07K14/805C12N15/11C12N15/86C12N2310/20C12N2750/14143C12N2800/80
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Quick Facts
Patent No.
US 12,110,499
App. No.
16/608,182
Granted
Oct 8, 2024
Kind
B2
Abstract

The present disclosure provides improved compositions for the homology directed repair of the human globin locus for the prevention, treatment, or amelioration of at least one symptom of a hemoglobinopathy.

Claims (26)

1. A method for increasing gamma globin expression in a hematopoietic stem or progenitor cell comprising introducing into the cell one or more engineered nucleases that cleave a target site set forth in SEQ ID NO: 9 and

a DNA donor repair template having the sequence as set forth in SEQ ID NOs: 17, 18, 19, 20, or 21,

whereby the DNA donor repair template is inserted into the cell genome by homology directed repair at a double strand break introduced by the one or more engineered nucleases.

2. The method of claim 1 , wherein the DNA donor repair template has the sequence as set forth in SEQ ID NO: 17.

3. The method of claim 1 , wherein the DNA donor repair template has the sequence as set forth in SEQ ID NO: 18.

4. The method of claim 1 , wherein the DNA donor repair template has the sequence as set forth in SEQ ID NO: 19.

5. The method of claim 1 , wherein the DNA donor repair template has the sequence as set forth in SEQ ID NO: 20.

6. The method of claim 1 , wherein the DNA donor repair template has the sequence as set forth in SEQ ID NO: 21.

7. A method for increasing gamma globin expression in a hematopoietic stem or progenitor cell comprising introducing into the cell

one or more engineered nucleases that cleave a target site set forth in SEQ ID NO: 9 and

a DNA donor repair template having at least 99% sequence identity to the sequence as set forth in SEQ ID NOs: 17, 18, 19, 20, or 21,

whereby the DNA donor repair template is inserted into the cell genome by homology directed repair at a double strand break introduced by the one or more engineered nucleases.

8. The method of claim 7 , wherein the DNA donor repair template has the sequence having at least 99% sequence identity to the sequence as set forth in SEQ ID NO: 17.

9. The method of claim 7 , wherein the DNA donor repair template has the sequence having at least 99% sequence identity to the sequence as set forth in SEQ ID NO: 18.

10. The method of claim 7 , wherein the DNA donor repair template has the sequence having at least 99% sequence identity to the sequence as set forth in SEQ ID NO: 19.

11. The method of claim 7 , wherein the DNA donor repair template has the sequence having at least 99% sequence identity to the sequence as set forth in SEQ ID NO: 20.

12. The method of claim 7 , wherein the DNA donor repair template has the sequence having at least 99% sequence identity to the sequence as set forth in SEQ ID NO: 21.

13. A method for increasing gamma globin expression in a hematopoietic stem or progenitor cell comprising introducing into the cell

one or more engineered nucleases that cleave a target site set forth in SEQ ID NO: 9 and

a DNA donor repair template having at least 98% sequence identity to the sequence as set forth in SEQ ID NOs: 17, 18, 19, 20, or 21,

whereby the DNA donor repair template is inserted into the cell genome by homology directed repair at a double strand break introduced by the one or more engineered nucleases.

14. The method of claim 13 , wherein the DNA donor repair template has the sequence having at least 98% sequence identity to the sequence as set forth in SEQ ID NO: 17.

15. The method of claim 13 , wherein the DNA donor repair template has the sequence having at least 98% sequence identity to the sequence as set forth in SEQ ID NO: 18.

16. The method of claim 13 , wherein the DNA donor repair template has the sequence having at least 98% sequence identity to the sequence as set forth in SEQ ID NO: 19.

17. The method of claim 13 , wherein the DNA donor repair template has the sequence having at least 98% sequence identity to the sequence as set forth in SEQ ID NO: 20.

18. The method of claim 13 , wherein the DNA donor repair template has the sequence having at least 98% sequence identity to the sequence as set forth in SEQ ID NO: 21.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 16, 2022
From: SCHARENBERG, ANDREW; JACOBY, KYLE; RAWLINGS, DAVID J.; LUX, CHRISTOPHER; PATTABHI, SOWMYA
To: SEATTLE CHILDREN'S HOSPITAL D/B/A SEATTLE CHILDREN'S RESEARCH INSTITUTE
Reel/Frame 061127/0044 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 16, 2022
From: KIEM, HANS-PETER; HUMBERT, OLIVIER M.
To: FRED HUTCHINSON CANCER RESEARCH CENTER
Reel/Frame 061127/0053 →
Continuity (2)
Provisional Application 62488927 · Apr 24, 2017
Related Publication 20210222201A1 · Jul 22, 2021