IP Library Granted Patent US 9,834,788
Granted Patent B2
US 9,834,788 · App. 14/000,836 · Granted Dec 5, 2017

AAV -vectors for use in gene therapy of choroideremia

Inventors: Robert Maclaren (Oxford, GB); Miguel Seabra (London, GB); Matthew John During (Columbus, OH)
Assignee: Oxford University Innovation Limited
C12N15/86A61K48/005C12N9/1085C12N2750/14143C12N2750/14171
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Quick Facts
Patent No.
US 9,834,788
App. No.
14/000,836
Granted
Dec 5, 2017
Kind
B2
Abstract

The present invention relates to gene therapy for treatment or prevention of choroideremia.

Claims (10)

1. A method of treating a human subject suffering from choroideremia, the method comprising: administering by subretinal injection a therapeutically effective amount of an AAV2 vector particle comprising a polynucleotide encoding a Rab escort protein 1 (REP1) having at least 97% sequence identity with SEQ ID NO: 3, wherein said polynucleotide is operably linked to a promoter, wherein one or more retinal pigmented epithelial cells and one or more rod photoreceptor cells of the human subject is transduced with the vector particle and wherein the REP1 is expressed in the one or more retinal pigmented epithelial cells and in the one or more rod photoreceptor cells, whereby the choroideremia is treated, arrested or palliated in the human subject.

2. The method according to claim 1 , wherein the vector particle comprises SEQ ID NO: 1 or a derivative thereof wherein the derivative is missing one or more sequences selected from the group consisting of: one inverted terminal repeat (ITR) sequence, the replication (rep) gene sequence, and the capsid (cap) gene sequence.

3. The method according to claim 1 , wherein the encoded REP1 comprises SEQ ID NO: 3.

4. The method according to claim 1 , wherein the polynucleotide sequence encoding REP1 has at least 90% sequence identity with SEQ ID NO:2.

5. The method according to claim 1 , wherein the promoter is a constitutively active promoter.

6. The method according to claim 1 , wherein the promoter is a retinal-cell specific promoter.

7. The method according to claim 1 wherein the vector particle comprises one or more regulatory sequences.

8. The method according to claim 7 wherein the vector particle comprises a polynucleotide having at least 70% sequence identity with SEQ ID NO: 5.

9. The method of claim 1 , wherein the promoter is an inducible promoter.

10. A method of treating a human subject suffering from choroideremia, the method comprising: administering to the subject by subretinal injection a therapeutically effective amount of an AAV2 vector particle comprising a polynucleotide encoding a Rab escort protein 1 (REP1) having at least 97% sequence identity with SEQ ID NO: 3, wherein said polynucleotide is operably linked to a chicken beta actin (CBA) promoter, wherein one or more retinal pigmented epithelial cells and one or more rod photoreceptor cells of the human subject is transduced with the vector particle and wherein the REP1 is expressed in the one or more retinal pigmented epithelial cells and in the one or more rod photoreceptor cells, whereby the choroideremia is treated, arrested or palliated in the human subject.

Assignments (2)
CHANGE OF NAME Recorded Aug 2, 2016
From: ISIS INNOVATION LIMITED
To: OXFORD UNIVERSITY INNOVATION LIMITED
Reel/Frame 039550/0045 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 18, 2013
From: MACLAREN, ROBERT; SEABRA, MIGUEL; DURING, MATTHEW JOHN
To: ISIS INNOVATION LIMITED
Reel/Frame 031806/0716 →
Priority Claims (1)
GB 1103062.4 · Feb 22, 2011 · national
Continuity (1)
Related Publication 20140107185A1 · Apr 17, 2014