Methods for adeno-associated viral vector production
View Patent ↗The invention relates to an adeno-associated virus (AAV) producer cell comprising nucleic acid sequences encoding: rep/cap gene; helper virus genes; and the DNA genome of the AAV vector particle, wherein the nucleic acid sequences are all integrated together at a single locus within the AAV producer cell genome. The invention also relates to nucleic acid vectors comprising a non-mammalian origin of replication and the ability to hold at least 25 kilobases (kb) of DNA, characterized in that the nucleic acid vectors comprise nucleic acid sequences encoding: rep/cap gene, and helper virus genes. The invention also relates to uses and methods using the nucleic acid vectors in order to produce stable AAV packaging and producer cell lines.
1. An isolated adeno-associated virus (AAV) producer cell comprising nucleic acid sequences encoding:
AAV rep/cap gene;
helper virus genes; and
a DNA genome of an AAV vector particle,
wherein said nucleic acid sequences are all integrated together at a single locus within the AAV producer cell genome; and wherein the cell further comprises a nucleic acid sequence encoding a short hairpin RNA (shRNA) targeting an AAV rep mRNA molecule encoded by the AAV rep gene and an inducible promoter operably linked to the nucleic acid sequence encoding the shRNA.
2. The AAV producer cell of claim 1 , wherein the AAV nucleic acid sequences are derived from AAV1, AAV2, AAV3, AAV4, AAV5, AAV6, AAV7, AAV8, AAV9, AAV10, AAV11, AAV12, AAV13 or combinations thereof.
3. The AAV producer cell of claim 2 , wherein the AAV nucleic acid sequences are derived from AAV2, AAV5 and/or AAV9.
4. The AAV producer cell of claim 1 , wherein the helper virus genes are derived from adenovirus.
5. The AAV producer cell of claim 4 , wherein the helper virus genes comprise all or part of E4, E2a and VA genes derived from adenovirus.
6. The AAV producer cell of claim 1 , which additionally comprises a transcription regulation element.
7. The AAV producer cell of claim 6 , wherein the transcription regulation element is a CMV promoter.
8. The AAV producer cell of claim 6 , wherein the transcription regulation element additionally comprises at least one Tet operon.
9. The AAV producer cell of claim 1 , which additionally comprises a tetracycline resistance operon repressor protein (TetR).
10. The AAV producer cell of claim 1 , which additionally comprises an insulator.
11. The AAV producer cell of claim 10 , wherein an insulator is present between each of the nucleic acid sequences.
12. The AAV producer cell of claim 1 , which additionally comprises a selectable marker.
13. The AAV producer cell of claim 12 , wherein the selectable marker is an amplifiable selection marker.
14. The AAV producer cell of claim 1 , which additionally comprises one or more transgenes.
15. The AAV producer cell of claim 1 , wherein the DNA genome of the AAV vector particle comprises one or more transgenes encoded between two AAV ITRs.
16. The AAV producer cell of claim 1 , wherein the cell is a mammalian cell.
17. The AAV producer cell of claim 1 , wherein the cell further comprises nucleic acid sequences encoding:
an adenovirus E1A gene;
an shRNA targeting an adenovirus E1A mRNA molecule encoded by the adenovirus E1A gene; and
an inducible promoter operably linked to the nucleic acid sequence encoding the shRNA targeting the adenovirus E1A mRNA molecule.
18. The AAV producer cell of claim 1 , wherein the cell further comprises a nucleic acid sequence of the shRNA targeting the AAV rep mRNA molecule or an E1A mRNA molecule, wherein the nucleic acid sequence is micro-RNA adapted for transcription by RNA polymerase II.
19. The AAV producer cell of claim 1 , wherein the inducible promoter is a Tet-responsive promoter, optionally wherein the Tet-responsive promoter is a Ptet-T6 promoter.
20. A nucleic acid vector comprising a non-mammalian origin of replication and the ability to hold at least 25 kilobases (kb) of DNA, characterized in that said nucleic acid vector comprises nucleic acid sequences encoding:
Adeno-associated virus (AAV) rep/cap gene, and
helper virus genes,
wherein the nucleic acid sequences encoding the AAV rep/cap gene and each of the helper virus genes are arranged as individual expression cassettes within the nucleic acid vector; and wherein the nucleic acid vector further comprises a nucleic acid sequence encoding a short hairpin RNA (shRNA) targeting an AAV rep mRNA molecule encoded by the AAV rep gene and an inducible promoter operably linked to the nucleic acid sequence encoding the shRNA.
21. The nucleic acid vector of claim 20 , which additionally comprises a nucleic acid sequence which encodes the DNA genome of the AAV vector particle.
22. The nucleic acid vector of claim 20 , wherein the vector is selected from: a bacterial artificial chromosome, a yeast artificial chromosome, a P1-derived artificial chromosome, a fosmid or a cosmid.
23. The nucleic acid vector of claim 22 , wherein the vector is a bacterial artificial chromosome.
24. The nucleic acid vector of claim 20 , wherein the nucleic acid vector further comprises nucleic acid sequences encoding:
an adenovirus E1A gene;
an shRNA targeting an adenovirus E1A mRNA molecule encoded by the adenovirus E1A gene; and
an inducible promoter operably linked to the nucleic acid sequence encoding the shRNA targeting the adenovirus E1A mRNA molecule.
25. The nucleic acid vector of claim 20 , wherein the nucleic acid vector further comprises a nucleic acid sequence of the shRNA targeting the AAV rep mRNA molecule or the E1A mRNA molecule, wherein the nucleic acid sequence is micro-RNA adapted for transcription by RNA polymerase II.
26. The nucleic acid vector of claim 20 , wherein the inducible promoter is a Tet-responsive promoter, optionally wherein the Tet-responsive promoter is a Ptet-T6 promoter.
27. A method of producing a stable AAV packaging cell line, comprising:
(a) introducing the nucleic acid vector of claim 20 into a culture of mammalian host cells; and
(b) selecting within the culture for a mammalian host cell which has the nucleic acid sequences encoded on the vector integrated into an endogenous chromosome of the mammalian host cell.
28. The method of claim 27 , wherein the mammalian cell is a HEK 293 cell.
29. An isolated AAV packaging cell obtained by the method of claim 27 .
30. A method of producing a replication defective AAV vector particle, comprising:
(a) introducing the nucleic acid vector of claim 20 into a culture of mammalian host cells;
(b) selecting within the culture for a mammalian host cell which has the nucleic acid sequences encoded on the vector integrated into an endogenous chromosome of the mammalian host cell; and
(c) further culturing the selected mammalian host cell under conditions in which the replication defective AAV vector particle is produced.
31. The method of claim 30 , additionally comprising isolating the replication defective AAV vector particle.
32. A replication defective AAV vector particle obtained by the method of claim 30 .