IP Library Granted Patent US 9,677,089
Granted Patent B2
US 9,677,089 · App. 15/084,615 · Granted Jun 13, 2017

Adeno-associated virus (AAV) serotype 8 sequences, vectors containing same, and uses therefor

Inventors: Guangping Gao (Westborough, MA); James M. Wilson (Glen Mills, PA); Mauricio R. Alvira (Philadelphia, PA)
Assignee: The Trustees of the University of Pennsylvania
C12N15/86A61K35/761A61K38/177A61K38/45A61K38/4846C07K14/005C07K14/705C07K14/755C12N7/00C12N9/1018C12N9/644A61K48/00C12N2750/14122C12N2750/14143C12N2750/14152C12N2830/008C12N2830/48C12N2830/85C12Y201/03003C12Y304/21022
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Quick Facts
Patent No.
US 9,677,089
App. No.
15/084,615
Granted
Jun 13, 2017
Kind
B2
Abstract

Sequences of a serotype 8 adeno-associated virus and vectors and host cells containing these sequences are provided. Also described are methods of using such host cells and vectors in production of rAAV particles.

Claims (20)

1. An adeno-associated virus (AAV)8 viral vector comprising an AAV8 capsid having packaged therein a heterologous gene operably linked to regulatory sequences which direct its expression, wherein the heterologous gene encodes factor IX, wherein the AAV8 capsid comprises a vp3 capsid protein having the sequence of aa 204 to 738 of SEQ ID NO: 2, or a sequence which is at least 95% identical to said sequence of aa 204 to 738 of SEQ ID NO: 2.

2. The vector according to claim 1 , further comprising one or more AAV inverted terminal repeat (ITR) sequence from an AAV heterologous to AAV8.

3. The vector according to claim 2 , wherein the one or more AAV ITR is from AAV2.

4. The vector according to claim 1 , wherein said vp3 capsid protein has a sequence which is at least 95% identical to the sequence of aa 204 to 738 of SEQ ID NO: 2.

5. The vector according to claim 4 , wherein said vp3 capsid protein has a sequence at least 99% identical to the sequence of aa 204 to 738 of SEQ ID NO: 2.

6. The vector according to claim 5 , wherein said vp3 capsid protein has the sequence of aa 204 to 738 of SEQ ID NO: 2.

7. The vector according to claim 1 , wherein said AAV8 capsid further comprises a vp1 capsid protein having a sequence which is at least 95% identical to the sequence of aa 1 to 738 of SEQ ID NO: 2.

8. The vector according to claim 7 , wherein said vp1 capsid protein has an amino acid sequence at least 99% identical to the sequence of aa 1 to 738 of SEQ ID NO: 2.

9. The vector according to claim 8 , wherein said vp1 capsid protein has the sequence of aa 1 to 738 of SEQ ID NO: 2.

10. The vector according to claim 1 , wherein said AAV8 capsid further comprises a vp2 capsid protein having a sequence which is at least 95% identical to the sequence of aa 138 to 738 of SEQ ID NO: 2.

11. The vector according to claim 10 , wherein said vp2 capsid protein has an amino acid sequence at least 99% identical to the sequence of aa 138 to 738 of SEQ ID NO: 2.

12. The vector according to claim 11 , wherein said vp2 capsid protein has the sequence of aa 138 to 738 of SEQ ID NO: 2.

13. A host cell containing the vector according to claim 1 in culture.

14. A method of delivering a heterologous gene encoding factor IX to a cell, said method comprising contacting said cell with the vector according to claim 1 .

15. The method according to claim 14 , comprising delivering said vector to a hepatocyte.

16. A method for treating hemophilia B, said method comprising the step of contacting a cell with a vector according to claim 1 , wherein said vector directs expression of factor IX.

17. A composition comprising at least the vector according to claim 1 and a pharmaceutically acceptable carrier.

18. A composition comprising at least the vector according to claim 1 and a preservative or chemical stabilizer.

19. A composition comprising at least an adeno-associated virus (AAV) vector and a physiologically compatible carrier, the AAV vector comprising an AAV capsid comprising at least an AAV8 vp3 capsid protein having a sequence comprising amino acids 204 to 738 of SEQ ID NO: 2 or an amino acid sequence at least 95% identical thereto, said capsid having packaged therein a heterologous gene operably linked to regulatory sequences which direct its expression, wherein the heterologous gene encodes factor IX.

20. A composition comprising at least an adeno-associated virus (AAV) vector and a physiologically compatible carrier, the AAV vector comprising an AAV capsid comprising at least an AAV8 vp1 capsid protein having a sequence comprising amino acids 1 to 738 of SEQ ID NO: 2 or an amino acid sequence at least 95% identical thereto, said capsid having packaged therein a heterologous gene operably linked to regulatory sequences which direct its expression, wherein the heterologous gene encodes factor IX.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 9, 2017
From: GAO, GUANGPING; WILSON, JAMES M; ALVIRA, MAURICIO R
To: THE TRUSTEES OF THE UNIVERSITY OF PENNSYLVANIA
Reel/Frame 041530/0486 →
Continuity (9)
Division 14598462 · Jan 16, 2005
Division 11981022 · Oct 31, 2007
Continuation 11899500 · Sep 6, 2007
Continuation 10423704 · Apr 25, 2003
Continuation In Part PCTUS0233630 · Nov 12, 2002
Provisional Application 60386122 · Jun 5, 2002
Provisional Application 60377133 · May 1, 2002
Provisional Application 60341151 · Dec 17, 2001
Related Publication 20160201088A1 · Jul 14, 2016