IP Library Granted Patent US 11,865,189
Granted Patent B2
US 11,865,189 · App. 15/536,725 · Granted Jan 9, 2024

Transgenic RPE cells overexpressing OTX2 for the treatment of retinal degeneration

Inventors: Thierry Leveillard (Maison-Alfort, FR); Christo Kole (Chatenay Malabry, FR); Jose-Alain Sahel (Paris, FR)
Assignees: SORBONNE UNIVERSITE; CENTRE NATIONAL DE LA RECHERCHE SCIENTIFIQUE; INSERM (INSTITUT NATIONAL DE LA SANTE ET DE LA RECHERCHE MEDICALE)
A61K48/0058A61K35/12A61K48/00C12N5/0621C12N5/16C12N7/00C12N15/8645C12N2510/00C12N2750/14141
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Quick Facts
Patent No.
US 11,865,189
App. No.
15/536,725
Granted
Jan 9, 2024
Kind
B2
Abstract

The present invention relates to methods and composition for use in the treatment of retinal degeneration, in particular retinal degeneration due to retinal pigment epithelium dysfunction.

Claims (18)

1. A method of treating retinitis pigmentosa in a mammal having retinitis pigmentosa, said method comprising the intraocular administration, by injection into the subretinal space of the eye of said mammal, of mammalian primary retinal pigment epithelial (RPE) cells or induced pluripotent stem cell-derived RPE cells overexpressing mammalian orthodenticle homeobox 2 protein (OTX2 protein), thereby increasing intracellular levels of OTX2 protein in the mammal, wherein the RPE cells overexpress OTX2 protein and comprise an AAV2 viral vector comprising a nucleic acid sequence encoding an OTX2 protein comprising SEQ ID NO: 15 or SEQ ID NO: 16.

2. The method according to claim 1 , wherein said OTX2 protein consists of SEQ ID NO: 15.

3. The method according to claim 1 , wherein said OTX2 protein consists of SEQ ID NO: 16.

4. The method according to claim 1 , wherein the nucleic acid sequence encoding said OTX2 protein is operably linked to one or more control sequences.

5. The method according to claim 1 , wherein the expression levels of OTX2 protein in said RPE cells overexpressing OTX2 are, after normalization, at least 1.5-fold higher than levels of OTX2 in RPE cells that do not comprise a viral vector for expressing OTX2 protein, said OTX2 protein comprising SEQ ID NO: 15 or SEQ ID NO: 16.

6. The method according to claim 1 , wherein the RPE cells are administered in the form of a pharmaceutical composition comprising a pharmaceutically acceptable carrier.

7. The method according to claim 6 , wherein said composition is formulated for subretinal injection.

8. The method according to claim 1 , wherein the RPE cells are obtained from a mammalian donor or from the mammal to be treated.

9. A method of treating age-related macular degeneration (ARMD) in a mammal having ARMD said method comprising the intraocular administration, by injection into the subretinal space of the eye of said mammal, of mammalian primary retinal pigment epithelial (RPE) cells or induced pluripotent stem cell-derived RPE cells overexpressing mammalian orthodenticle homeobox 2 protein (OTX2 protein), thereby increasing intracellular levels of OTX2 protein in the mammal, wherein the RPE cells overexpress OTX2 protein and comprise an AAV2 viral vector comprising a nucleic acid sequence encoding an OTX2 protein comprising SEQ ID NO: 15 or SEQ ID NO: 16.

10. The method according to claim 9 , wherein said OTX2 protein consists of SEQ ID NO: 15.

11. The method according to claim 9 , wherein said OTX2 protein consists of SEQ ID NO: 16.

12. The method according to claim 9 , wherein the nucleic acid sequence encoding said OTX2 protein is operably linked to one or more control sequences.

13. The method according to claim 9 , wherein the expression levels of OTX2 protein in said RPE cells overexpressing OTX2 are, after normalization, at least 1.5-fold higher than levels of OTX2 in RPE cells that do not comprise a viral vector for expressing OTX2 protein, said OTX2 protein comprising SEQ ID NO: 15 or SEQ ID NO: 16.

14. The method according to claim 9 , wherein the RPE cells are administered in the form of a pharmaceutical composition comprising a pharmaceutically acceptable carrier.

15. The method according to claim 14 , wherein said composition is formulated for subretinal injection.

16. The method according to claim 9 , wherein the RPE cells are obtained from a mammalian donor or from the mammal to be treated.

17. The method according to claim 1 , wherein said retinitis pigmentosa results from degeneration or dysfunction of retinal pigmented epithelium.

18. The method according to claim 9 , wherein said ARMD results from degeneration or dysfunction of retinal pigmented epithelium.

Assignments (2)
MERGER AND CHANGE OF NAME Recorded Aug 24, 2018
From: UNIVERSITE PIERRE ET MARIE CURIE (PARIS 6); SORBONNE UNIVERSITE
To: SORBONNE UNIVERSITE
Reel/Frame 046691/0233 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 27, 2017
From: LÉVEILLARD, THIERRY; KOLE, CHRISTO; SAHEL, JOSÉ-ALAIN
To: UNIVERSITE PIERRE ET MARIE CURIE (PARIS 6); CENTRE NATIONAL DE LA RECHERCHE SCIENTIFIQUE; INSERM (INSTITUT NATIONAL DE LA SANTE ET DE LA RECHERCHE MEDICALE)
Reel/Frame 043709/0717 →
Priority Claims (1)
EP 14307069 · Dec 18, 2014 · regional
Continuity (1)
Related Publication 20170348434A1 · Dec 7, 2017