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PMID: 10455400 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

High-titer recombinant adeno-associated virus production utilizing a recombinant herpes simplex virus type I vector expressing AAV-2 Rep and Cap.

Gene therapy ·Vol. 6 ·No. 6 ·1999-06-00 ·Pages 986-93

Conway JE, Rhys CM, Zolotukhin I, Zolotukhin S, Muzyczka N, Hayward GS, Byrne BJ

Abstract

Recombinant adeno-associated virus type 2 (rAAV) vectors have recently been used to achieve long-term, high level transduction in vivo. Further development of rAAV vectors for clinical use requires significant technological improvements in large-scale vector production. In order to facilitate the production of rAAV vectors, a recombinant herpes simplex virus type I vector (rHSV-1) which does not produce ICP27, has been engineered to express the AAV-2 rep and cap genes. The optimal dose of this vector, d27.1-rc, for AAV production has been determined and results in a yield of 380 expression units (EU) of AAV-GFP produced from 293 cells following transfection with AAV-GFP plasmid DNA. In addition, d27.1-rc was also efficient at producing rAAV from cell lines that have an integrated AAV-GFP provirus. Up to 480 EU/cell of AAV-GFP could be produced from the cell line GFP-92, a proviral, 293 derived cell line. Effective amplification of rAAV vectors introduced into 293 cells by infection was also demonstrated. Passage of rAAV with d27. 1-rc results in up to 200-fold amplification of AAV-GFP with each passage after coinfection of the vectors. Efficient, large-scale production (>109 cells) of AAV-GFP from a proviral cell line was also achieved and these stocks were free of replication-competent AAV. The described rHSV-1 vector provides a novel, simple and flexible way to introduce the AAV-2 rep and cap genes and helper virus functions required to produce high-titer rAAV preparations from any rAAV proviral construct. The efficiency and potential for scalable delivery of d27.1-rc to producer cell cultures should facilitate the production of sufficient quantities of rAAV vectors for clinical application.

MeSH Terms
Blotting, Western Cell Line Dependovirus Fluorescent Antibody Technique Genetic Therapy/methods Genetic Vectors Humans Simplexvirus Transfection Virology/methods Virus Replication
Authors & Affiliations
7 authors, click to expand affiliations / ORCID
Conway J E
Department of Pharmacology and Molecular Sciences, Johns Hopkins University School of Medicine, Baltimore, MD, USA.
Rhys C M
Zolotukhin I
Zolotukhin S
Muzyczka N
Hayward G S
Byrne B J
Article Info
Journal
Gene therapy
Abbr.
Gene Ther
ISSN
0969-7128
Published
1999-06-00
Pages
986-93
Language
English
Region
England
NLM ID
9421525
Subset
IM
Grants
NHLBI NIH HHS · HL59412 · United States
NCI NIH HHS · T32-CA-09243 · United States
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