IP Library Granted Patent US 12,139,720
Granted Patent B2
US 12,139,720 · App. 16/618,226 · Granted Nov 12, 2024

Recombinant lentiviral vector for stem cell- based gene therapy of sickle cell disorder

Inventors: Annarita Miccio (Paris, FR); Vasco Meneghini (Bretigny-sur-Orge, FR)
Assignees: INSTITUT NATIONAL DE LA SANTE ET DE LA RECHERCHE MEDICALE (INSERM); UNIVERSITE PARIS DESCARTES; ASSISTANCE PUBLIQUE-HOPITAUX DE PARIS; IMAGINE—INSTITUT DES MALADIES GENETIQUES NECKER ENFANTS MALADES
C12N15/86A61K38/42C12N5/0607C12N9/22C12N2310/20C12N2740/15043C12N2830/40C12N2830/48
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Quick Facts
Patent No.
US 12,139,720
App. No.
16/618,226
Granted
Nov 12, 2024
Kind
B2
Abstract

This invention relates to recombinant lentiviral vectors, compositions thereof, the use of the vectors or the compositions thereof, kits of parts comprising said vectors or compositions thereof and a catalytically active Cas9 or Cpf1 protein, methods for modifying the genome of a hematopoietic stem/progenitor cell (HSPC), and the HSPC obtainable by such methods.

Claims (66)

1. A recombinant lentiviral vector comprising in its genome:

(i) a nucleotide sequence encoding a protein that has a therapeutic effect, said protein being selected from the group consisting of delta-globin and gamma globin; and

(ii) a nucleotide sequence encoding a guide RNA (gRNA) that comprises a spacer adapted to bind to a target nucleotide sequence, said target nucleotide sequence being:

a. within the coding sequence or within a transcribed non-coding sequence of a target gene, said target gene being selected from beta-globin gene and BCL11A gene, or

b. within the promoter region of a target gene, wherein said target gene is a gamma-globin gene when the nucleotide sequence (i) encoding the protein that has the therapeutic effect is delta-globin.

2. The recombinant lentiviral vector according to claim 1 , wherein the protein that has a therapeutic effect is selected from the group consisting of human delta-globin and human gamma-globin.

3. A recombinant lentiviral vector comprising in its genome:

(i) a nucleotide sequence encoding a protein that has a therapeutic effect, said protein being human beta AS3 globin; and

(ii) a nucleotide sequence encoding a guide RNA (gRNA) that comprises a spacer adapted to bind to a target nucleotide sequence, said target nucleotide sequence being:

a. within the coding sequence or within a transcribed non-coding sequence of a target gene, said target gene being BCL11A gene, or

b. within the promoter region of a target gene, said target gene being gamma-globin gene.

4. The recombinant lentiviral vector according to claim 1 , wherein the beta-globin gene, gamma-globin gene or BCL11A gene is human.

5. A composition comprising the recombinant lentiviral vector according to claim 1 or a plurality of said recombinant lentiviral vectors.

6. A kit comprising:

the recombinant lentiviral vector according to claim 1 ; and

a catalytically active Cas9 or Cpf1 protein or a nucleotide sequence encoding a catalytically active Cas9 or Cpf1 protein.

7. The recombinant lentiviral vector according to claim 1 for introducing into a hematopoietic stem/progenitor cell (HSPC)

(i) the nucleotide sequence encoding a protein that has a therapeutic effect, said protein being selected from the group consisting of delta-globin and gamma globin, and

(ii) the nucleotide sequence encoding a guide RNA (gRNA) that comprises a spacer adapted to bind to a target nucleotide sequence, said target nucleotide sequence is:

a. within the coding sequence or within a transcribed non-coding sequence of a target gene, said target gene is selected from beta-globin gene and BCL11A gene, or

b. within the promoter region of a target gene, wherein said target gene is a gamma-globin gene when the nucleotide sequence (i) encoding the protein that has the therapeutic effect is delta-globin.

8. A method for modifying the genome of a hematopoietic stem/progenitor cell (HSPC), in vitro or ex vivo, comprising the steps of:

a) contacting a HSPC with a recombinant lentiviral vector of claim 1 to obtain a transduced HSPC, wherein the lentiviral vector is integrated into the genome of said HSPC; and

b) introducing into the transduced HSPC a catalytically active Cas9 or Cpf1 protein or a nucleotide sequence encoding a catalytically active Cas9 or Cpf1 protein, said catalytically active Cas9 or Cpf1 protein disrupts the expression and/or the function of the target gene when introduced or expressed into the transduced HSPC.

9. A method for preparing a genetically modified hematopoietic stem/progenitor cell (HSPC), in vitro or ex vivo, comprising the steps of:

a) contacting a HSPC with a recombinant lentiviral vector of claim 1 to obtain a transduced HSPC, wherein the lentiviral vector is integrated into the genome of said HSPC; and

b) introducing into the transduced HSPC a catalytically active Cas9 or Cpf1 protein or a nucleotide sequence encoding a catalytically active Cas9 or Cpf1 protein, said catalytically active Cas9 or Cpf1 protein disrupts the expression and/or the function of the target gene when introduced or expressed into the transduced HSPC.

10. A kit comprising:

a composition according to claim 5 ; and

a catalytically active Cas9 or Cpf1 protein or a nucleotide sequence encoding a catalytically active Cas9 or Cpf1 protein.

11. The composition according to claim 5 for introducing into a hematopoietic stem/progenitor cell (HSPC)

(i) the nucleotide sequence encoding a protein that has a therapeutic effect, said protein being selected from the group consisting of delta-globin and gamma globin, and

(ii) the nucleotide sequence encoding a guide RNA (gRNA) that comprises a spacer adapted to bind to a target nucleotide sequence, said target nucleotide sequence is:

a. within the coding sequence or within a transcribed non-coding sequence of a target gene, said target gene being selected from beta-globin gene and BCL11A gene, or

b. within the promoter region of a target gene, wherein said target gene is a gamma-globin gene when the nucleotide sequence (i) encoding the protein that has the therapeutic effect is delta-globin.

12. The kit according to claim 6 for use in introducing into a hematopoietic stem/progenitor cell (HSPC)

(i) the nucleotide sequence encoding a protein that has a therapeutic effect, said protein being selected from the group consisting of delta-globin and gamma globin, and

(ii) the nucleotide sequence encoding a guide RNA (gRNA) that comprises a spacer adapted to bind to a target nucleotide sequence, said target nucleotide sequence is:

a. within the coding sequence or within a transcribed non-coding sequence of a target gene, said target gene being selected from beta-globin gene and BCL11A gene, or

b. within the promoter region of a target gene, wherein said target gene is a gamma-globin gene when the nucleotide sequence (i) encoding the protein that has the therapeutic effect is delta-globin.

13. A method for modifying the genome of a hematopoietic stem/progenitor cell (HSPC), in vitro or ex vivo, comprising the steps of:

a) contacting a HSPC with a composition according to claim 5 to obtain a transduced HSPC, wherein the lentiviral vector is integrated into the genome of said HSPC; and

b) introducing into the transduced HSPC a catalytically active Cas9 or Cpf1 protein or a nucleotide sequence encoding a catalytically active Cas9 or Cpf1 protein, wherein said catalytically active Cas9 or Cpf1 protein disrupts the expression and/or the function of the target gene when introduced or expressed into the transduced HSPC.

14. A method for preparing a genetically modified hematopoietic stem/progenitor cell (HSPC), in vitro or ex vivo, comprising the steps of:

a) contacting a HSPC with a composition according to claim 5 to obtain a transduced HSPC, wherein the lentiviral vector is integrated into the genome of said HSPC; and

b) introducing into the transduced HSPC a catalytically active Cas9 or Cpf1 protein or a nucleotide sequence encoding a catalytically active Cas9 or Cpf1 protein, wherein said catalytically active Cas9 or Cpf1 protein disrupts the expression and/or the function of the target gene when introduced or expressed into the transduced HSPC.

15. A composition comprising a recombinant lentiviral vector according to claim 3 or a plurality of said recombinant lentiviral vectors.

16. A kit comprising: the recombinant lentiviral vector according to claim 3 ; and

a catalytically active Cas9 or Cpf1 protein or a nucleotide sequence encoding a catalytically active Cas9 or Cpf1 protein.

17. A recombinant lentiviral vector comprising in its genome:

(i) a nucleotide sequence encoding a protein that has a therapeutic effect, said protein being selected from the group consisting of beta-globin, gamma-globin, and delta-globin; and

(ii) a nucleotide sequence encoding a guide RNA (gRNA) that comprises a spacer adapted to bind to a target nucleotide sequence, said target nucleotide sequence being:

a. within the coding sequence or within a transcribed non-coding sequence of a target gene, said target gene being BCL11A gene, or

b. within the promoter region of a target gene, wherein said target gene is a gamma-globin gene when the nucleotide sequence (i) encoding the protein that has the therapeutic effect is selected from the group consisting of delta-globin and beta-globin.

18. A composition comprising a recombinant lentiviral vector according to claim 17 or a plurality of said recombinant lentiviral vectors.

19. A kit comprising the recombinant lentiviral vector according to claim 17 ; and

a catalytically active Cas9 or Cpf1 protein or a nucleotide sequence encoding a catalytically active Cas9 or Cpf1 protein.

20. A recombinant lentiviral integrative vector comprising in its genome:

(i) a nucleotide sequence encoding a protein that has a therapeutic effect, said protein being selected from the group consisting of beta-globin, gamma-globin, and delta-globin; and

(ii) a nucleotide sequence encoding a guide RNA (gRNA) that comprises a spacer adapted to bind to a target nucleotide sequence, said target nucleotide sequence is:

(a) within the coding sequence or within a transcribed non-coding sequence of a target gene, said target gene being selected from beta-globin gene and BCL11A gene, or

(b) within the promoter region of a target gene, wherein said target gene is a gamma-globin gene when the nucleotide sequence (i) encoding the protein that has the therapeutic effect is selected from the group consisting of delta-globin and beta-globin.

21. A composition comprising a recombinant lentiviral vector according to claim 20 or a plurality of said recombinant lentiviral vectors.

22. A kit comprising:

the recombinant lentiviral integrative vector according to claim 20 ; and

a catalytically active Cas9 or Cpf1 protein or a nucleotide sequence encoding a catalytically active Cas9 or Cpf1 protein.

Assignments (3)
CHANGE OF NAME Recorded May 12, 2022
From: UNIVERSITE DE PARIS
To: UNIVERSITÉ PARIS CITÉ
Reel/Frame 059988/0388 →
MERGER Recorded May 12, 2022
From: UNIVERSITE PARIS DESCARTES
To: UNIVERSITE DE PARIS
Reel/Frame 060044/0856 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 10, 2020
From: MICCIO, ANNARITA; MENEGHINI, VASCO
To: INSTITUT NATIONAL DE LA SANTE ET DE LA RECHERCHE MEDICALE (INSERM); UNIVERSITE PARIS DESCARTES; ASSISTANCE PUBLIQUE - HOPITAUX DE PARIS; IMAGINE - INSTITUT DES MALADIES GENETIQUES NECKER ENFANTS MALADES
Reel/Frame 052067/0230 →