IP Library › Granted Patent US 12,234,476
Granted Patent B2
US 12,234,476 · App. 16/076,946 · Granted Feb 25, 2025

VCN enhancer compositions and methods of using the same

Inventors: Melissa Bonner (Natick, MA); Olivier Negre (Cambridge, MA)
Assignee: BLUEBIRD BIO, INC.
C12N15/867C12N5/0647C12N7/00C12N2501/02C12N2501/999C12N2510/00C12N2740/15011C12N2740/15041C12N2740/16011C12N2740/16041C12N2740/16043
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Quick Facts
Patent No.
US 12,234,476
App. No.
16/076,946
Granted
Feb 25, 2025
Kind
B2
Abstract

The invention provides improved gene therapy methods and compositions.

Claims (29)

1. A method of increasing the vector copy number (VCN) in a population of CD34+ hematopoietic stem or progenitor cells comprising culturing the cells for at least two hours in the presence of: (1) a lentiviral vector at a multiplicity of infection (MOI) of about 10 to about 30; (2) a prostaglandin E 2 (PGE 2 ), or 16,16-dimethyl PGE 2 ; and (3) poloxamer 338, wherein the increase of VCN achieved by culturing the cells for at least two hours in the presence of the lentiviral vector, poloxamer 338 and one of PGE 2 or 16,16-dimethyl PGE 2 is further enhanced beyond the increased VCN achieved by culturing the cells for at least two hours in the presence of the lentiviral vector and one of PGE 2 or 16,16-dimethyl PGE 2 and the absence of poloxamer 338.

2. The method of claim 1 , wherein the hematopoietic stem or progenitor cells are selected for CD34 + expression prior to transduction.

3. The method of claim 1 , wherein the CD34+ hematopoietic stem or progenitor cells comprise the B-globin alleles selected from the group consisting of: β E /β 0 , β C /β 0 , β 0 /β 0 , β E /β E , β C /β + , β E /β + , β 0 /β + , β + /β + , β C /β C , β E /β S , β 0 /β S , β C /β S , β + /β S and β S /β S .

4. The method of claim 1 , wherein the CD34+ hematopoietic stem or progenitor cells comprise the B-globin alleles selected from the group consisting of: β E /β 0 , β 0 /β 0 , β E /β E , β E /β + , β 0 /β + , and β + /β + .

5. The method of claim 1 , wherein the lentiviral vector is cultured with the cells at an MOI of about 10 to about 25, or about 10 to about 20.

6. The method of claim 1 , wherein the lentiviral vector is cultured with the cells at an MOI of about 10, about 11, about 12, about 13, about 14, about 15, about 16, about 17, about 18, about 19, about 20, about 21, about 22, about 23, about 24, about 25, about 26, about 27, about 28, about 29 or about 30.

7. The method of claim 1 , wherein the lentiviral vector is derived from an HIV-1 lentivirus.

8. The method of claim 1 , wherein the lentiviral vector comprises:

a) a 5′ long terminal (LTR);

b) a Psi (Ψ) packaging signal;

c) an RNA export element;

d) a lentiviral central polypurine tract (cPPT);

e) a promoter operably linked to a polynucleotide of interest; and

f) a SIN 3′ LTR.

9. The method of claim 1 , wherein the lentiviral vector comprises:

a) a 5′ long terminal (LTR) comprising a cytomegalovirus (CMV) promoter;

b) a Psi (Ψ) packaging signal;

c) a Rev response element (RRE);

d) a lentiviral central polypurine tract (cPPT);

e) a human β-globin LCR and human β-globin promoter operably linked to a polynucleotide encoding a globin; and

f) a self-inactivating (SIN) 3′ LTR that comprises a synthetic polyadenylation sequence.

10. The method of claim 9 , wherein the globin is selected from the group consisting of: a human β-globin, a human δ-globin, a human γ-globin, a human β A-T87Q -globin, a human β A-G16D/E22A/T87Q -globin, and a human β A-T87Q/K95E/K120E -globin.

11. The method of claim 1 , wherein the lentiviral vector is an AnkT9W vector, a T9Ank2W vector, a TNS9 vector, a lentiglobin HPV569 vector, a lentiglobin BB305 vector, a BG-1 vector, a BGM-1 vector, a d432BAγ vector, a mLARβΔγV5 vector, a GLOBE vector, a G-GLOBE vector, a βAS3-FB vector, a V5 vector, a V5m3 vector, a V5m3-400 vector, a G9 vector, or a BCL11A shmir vector.

12. The method of claim 1 , wherein the cells are cultured in the presence of PGE 2 .

13. The method of claim 1 , wherein the cells are cultured in the presence of 16,16-dimethyl PGE 2 .

14. The method of claim 1 , wherein the PGE 2 or 16,16-dimethyl PGE 2 is present in the culture in a concentration of about 10 μM to about 100 μM.

15. The method of claim 14 , wherein the PGE 2 or 16,16-dimethyl PGE 2 is present in the culture in a concentration of about 10 μM to about 50 μM.

16. The method of claim 1 , wherein the poloxamer 338 is present in the culture in a concentration of about 50 μg/mL to about 1000 μg/mL.

17. The method of claim 16 , wherein the poloxamer 338 is present in the culture in a concentration of about 62.5 μg/mL to less than 1000 μg/mL.

Assignments (3)
CHANGE OF NAME Recorded Sep 25, 2025
From: BLUEBIRD BIO, INC.
To: GENETIX BIOTHERAPEUTICS INC.
Reel/Frame 072955/0154 →
SECURITY INTEREST Recorded Mar 15, 2024
From: BLUEBIRD BIO, INC.
To: HERCULES CAPITAL, INC., AS AGENT
Reel/Frame 066801/0818 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 19, 2018
From: BONNER, MELISSA; NEGRE, OLIVIER
To: BLUEBIRD BIO, INC.
Reel/Frame 047237/0817 →
Continuity (5)
Provisional Application 62294615 · Feb 12, 2016
Provisional Application 62313571 · Mar 25, 2016
Provisional Application 62417085 · Nov 3, 2016
Provisional Application 62429514 · Dec 2, 2016
Related Publication 20190284533A1 · Sep 19, 2019
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