Gene therapy for treating peroxisomal disorders

Patent metadata

Field	Value
Publication number	US-11793887-B2
Application number	US-201816615941-A
Country	US
Kind code	B2
Filing date	May 31, 2018
Priority date	May 31, 2017
Publication date	Oct 24, 2023
Grant date	Oct 24, 2023

Abstract

Methods and compositions are provided for treatment of peroxisomal biogenesis disorders (PBDs). More particularly, recombinant adeno-associated viruses (rAAV) provided in the form of compositions are used to deliver a nucleic acid encoding human PEX1 to host cells. The rAAVs comprise a AAV capsid, and packaged therein a vector genome comprising an AAV 5′ inverted terminal repeat (ITR) sequence; a promoter; a coding sequence encoding a human PEX1; and an AAV 3′ ITR.

First claim

What is claimed is:

1. A method of treating a deficiency in peroxisome biogenesis factor 1 (PEX1) in a subject in need thereof, comprising directly administering to an eye of the subject a recombinant adeno-associated virus (rAAV) comprising an AAV capsid having packaged therein a vector genome comprising a nucleic acid sequence that encodes human PEX1, thereby improving visual function in the subject.

2. The method according to claim 1 , wherein the rAAV is delivered in a dosage of from about 1×10 9 to about 1×10 13 vector genomes per eye (vg/eye) in an aqueous suspension.

3. The method according to claim 1 , wherein the rAAV is administered subretinally.

4. The method according to claim 1 , wherein the rAAV is administered in a dosage of from 1×10 9 to 1×10 13 vg/eye in a volume comprising about 150 microliters, thereby treating the PEX1 deficiency in said subject.

5. The method according to claim 1 , wherein rAAV is administered in a volume of between 150 to 800 microliters.

6. The method according to claim 1 , wherein the subject is human.

7. The method according to claim 1 , wherein the subject has a Zellweger Spectrum Disorder selected from Zellweger syndrome, neonatal adrenoleukodystrophy, or infantile Refsum disease.

8. The method of claim 1 , wherein the human PEX1 comprises the amino acid sequence of SEQ ID NO 7, or a sequence at least 90% identical to the amino acid sequence set forth in SEQ ID NO: 7.

9. The method of claim 1 , wherein nucleic acid sequence comprises SEQ ID NO: 1 or a sequence at least 80% identical to SEQ ID NO: 1.

10. The method of claim 9 , wherein the nucleic acid sequence comprises SEQ ID NO: 1.

11. The method of claim 1 , wherein AAV capsid is selected from the group consisting of an AAV7m8 capsid or variant thereof, an AAV8 capsid or a variant thereof, an AAV6 capsid or variant thereof, an AAV9 capsid or variant thereof, an AAV7 capsid or variant thereof, an AAV5 capsid or variant thereof, an AAV2 capsid or variant thereof, an AAV1 capsid or variant thereof, an AAV3 capsid or variant thereof, and an AAV4 capsid or variant thereof.

12. The method of claim 1 , wherein the rAAV comprises an AAV8 capsid.

13. The method of claim 1 , wherein the vector genome comprises
(a) an AAV 5′ inverted terminal repeat (ITR) sequence;
(b) a promoter;
(c) a coding sequence encoding a human PEX1; and
(d) an AAV 3′ ITR.

14. The method of claim 13 , wherein the promoter is a cytomegalovirus (CMV) promoter.

15. The method of claim 13 , wherein the promoter is a hybrid promoter comprising a CMV enhancer sequence and a chicken beta actin (CBA) promoter sequence.

16. The method of claim 13 , wherein the vector genome further comprises a polyA.

17. The method of claim 1 , wherein the vector genome comprises SEQ ID NO: 6, SEQ ID NO: 8, nucleotides 1253 to 7390 of SEQ ID NO: 9, nucleotides 1253 to 5960 of SEQ ID NO: 10, nucleotides 1253 to 6196 of SEQ ID NO: 11, nucleotides 1253 to 5951 of SEQ ID NO: 12 or nucleotides 1253 to 6235 of SEQ ID NO:13.

18. The method according to claim 1 , wherein said rAAV is administered in a dosage of from 1×10 9 to 1×10 13 vg/eye in a volume comprising at least 150 microliters, thereby treating the PEX1 disorder in said subject.

19. The method of claim 1 , wherein the rAAV comprises an AAV2 capsid.

20. The method according to claim 1 , wherein the rAAV is administered intravitreally.

21. The method according to claim 1 , wherein visual function is assessed using electroretinograms (ERGs) to examine rod and cone photoreceptor function, pupillometry visual acuity, contrast sensitivity color vision testing, visual field testing (Humphrey visual fields/Goldmann visual fields), perimetry mobility test (obstacle course), or reading speed test.

Assignees

• Univ Pennsylvania
• Univ Southern California
• The Research Institute Of The Mcgill Univ Health Centre
• The Research Institute Of Mcgill Univ Health Centre

Inventors

• Braverman Nancy
• Argyriou Catherine
• Hacia Joseph
• Bennett Jean
• Sun Junwei
• Song Ji Yun
• Mcdougald Devin

Classifications

• A61K48/005 Primary

  characterised by an aspect of the 'active' part of the composition delivered, i.e. the nucleic acid delivered · CPC title

• A61K35/761

  Adenovirus · CPC title

• C12N9/14

  Hydrolases (3) · CPC title

• C12N15/86

  Viral vectors · CPC title

• C07H21/04

  with deoxyribosyl as saccharide radical · CPC title