IP Library Granted Patent US 10,137,176
Granted Patent B2
US 10,137,176 · App. 14/769,596 · Granted Nov 27, 2018

Compositions and methods for treating MPSI

Inventors: James M. Wilson (Philadelphia, PA); Brittney L. Gurda (Collegeville, PA)
Assignee: The Trustee of the University of Pennsylvania
A61K38/47A61K9/0019A61K35/76A61K48/0058C12N7/00C12N9/2402C12N2750/14143C12Y302/01076
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Quick Facts
Patent No.
US 10,137,176
App. No.
14/769,596
Granted
Nov 27, 2018
Kind
B2
Abstract

A vector having an expression cassette having a hIDUA gene having a sequence of SEQ ID NO: 1 or a sequence at least about 95% identical thereto which encodes a functional human alpha-L-iduronidase is provided. The vector may be production vector or a rAAV8. Also provided are compositions containing these vectors and methods of treating MPSI and the symptoms associated with Hurler, Hurle-Scheie and Scheie syndromes.

Claims (25)

1. A recombinant adeno-associated virus (rAAV) particle having an AAV capsid and having packaged therein a 5′ inverted terminal repeat (ITR), a human alpha-L-iduronidase (hIDUA) gene under the control of regulatory sequences which control expression thereof, and an AAV 3′ ITR, wherein said hIDUA gene has a sequence of SEQ ID NO: 1 or a sequence at least about 95% identical to SEQ ID NO: 1 which encodes a functional human alpha-L-iduronidase.

2. The rAAV particle according to claim 1 , wherein said hIDUA gene is expressed under the control of a liver-specific promoter.

3. The rAAV particle according to claim 2 , wherein the promoter is a thyroxin binding globulin (TBG) promoter.

4. The rAAV particle according to claim 1 , wherein the regulatory sequences comprise one or more enhancers.

5. The rAAV particle according to claim 4 , wherein the enhancers are the same or different.

6. The rAAV particle according to claim 4 , wherein the enhancers are selected from the group consisting of an intron, a cytomegalovirus (CMV) enhancer, and an Alpha mic/bik enhancer.

7. The rAAV particle according to claim 6 , wherein more than one copy of a selected enhancer are present in the vector.

8. The rAAV particle according to claim 7 , wherein the more than one copy of the enhancer are located in tandem.

9. The rAAV particle according to claim 1 , wherein the rAAV particle comprises an AAV capsid selected from AAV8 and AAV9.

10. The rAAV particle according to claim 9 , wherein the rAAV particle is pseudotyped.

11. The rAAV particle according to claim 1 , wherein the ITRs are from an AAV2.

12. The rAAV particle according to claim 1 , having an AAV8 capsid and having packaged therein an AAV2 5′ ITR, a hIDUA gene of SEQ ID NO: 1, under the control of regulatory sequences which control expression thereof, and an AAV2 3′ ITR, wherein the control regulatory sequences comprises a liver-specific TBG promoter, tandem repeats of alpha mic/bic enhancers, an intron sequence, and a poly A.

13. A composition useful for treating mucopolysaccharidosis type I (MPS I) comprising the rAAV particle according to claim 1 and a pharmaceutically acceptable carrier.

14. A method for treating MPS I comprising delivering an effective amount of a composition comprising a pharmaceutically acceptable carrier and the rAAV particle according to claim 1 to a subject.

15. The method according to claim 14 , wherein said rAAV particle is delivered intravenously.

16. The method according to claim 15 , wherein about 3×10 9 to about 3×10 12 genome copies of the rAAV is delivered to the subject.

17. The rAAV particle according to claim 1 , wherein the functional human alpha-L-iduronidase is selected from:

(a) about amino acid (aa) 1 to about aa 653 of SEQ ID NO: 2;

(b) a synthetic human enzyme comprising a heterologous leader sequence fused to about aa 27 to about aa 653 of SEQ ID NO: 2; and

(c) a variant of amino acid sequence of SEQ ID NO:2 having one or more of the modifications comprising: an H to Q reduction at amino acid position 82 (SEQ ID NO:8); a change from R to Q at position 105 (SEQ ID NO: 9); a change from G to R at position 116 (SEQ ID NO: 10); a change from V to A at position 279 (SEQ ID NO: 11); a change from L to R at position 346 (SEQ ID NO: 12); a change from A to T at position 361 (SEQ ID NO: 13); a change from H to N at position 449 (SEQ ID NO: 14); a change from V to I at position 454 (SEQ ID NO: 15); a change from A to T at position 591 (SEQ ID NO: 16); and a change from A to T at position 622 (SEQ ID NO: 17).

18. The rAAV particle according to claim 1 , wherein the regulatory sequences further comprise a poly A.

19. The rAAV particle according to claim 1 , wherein the hIDUA has the sequence at least 95% identical to SEQ ID NO: 1 which encodes a functional human alpha-L-iduronidase.

20. The rAAV particle according to claim 1 , wherein the hIDUA has the sequence at least 97% identical to SEQ ID NO: 1 which encodes a functional human alpha-L-iduronidase.

21. The rAAV particle according to claim 1 , wherein the hIDUA has the sequence at least 99% identical to SEQ ID NO: 1 which encodes a functional human alpha-L-iduronidase.

22. The rAAV particle according to claim 1 , wherein the hIDUA gene has the sequence of SEQ ID NO: 1.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 3, 2018
From: WILSON, JAMES M.; GURDA, BRITTNEY L.
To: THE TRUSTEES OF THE UNIVERSITY OF PENNSYLVANIA
Reel/Frame 046547/0176 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 6, 2015
From: WILSON, JAMES M.; GURDA, BRITTNEY L.
To: THE TRUSTEES OF THE UNIVERSITY OF PENNSYLVANIA
Reel/Frame 036732/0801 →
Continuity (2)
Provisional Application 61788724 · Mar 15, 2013
Related Publication 20160000887A1 · Jan 7, 2016