Source:http://linkedlifedata.com/resource/pubmed/id/18923452
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
2
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pubmed:dateCreated |
2009-2-12
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pubmed:abstractText |
Recombinant herpes simplex virus type 1 (rHSV)-assisted recombinant adeno-associated virus (rAAV) vector production provides a highly efficient and scalable method for manufacture of clinical grade rAAV vectors. Here, we present an rHSV co-infection system for rAAV production, which uses two ICP27-deficient rHSV constructs, one bearing the rep2 and cap (1, 2 or 9) genes of rAAV, and the second bearing an AAV2 ITR-gene of interest (GOI) cassette. The optimum rAAV production parameters were defined by producing rAAV2/GFP in HEK293 cells, yielding greater than 9000 infectious particles per cell with a 14:1 DNase resistance particle to infectious particle (DRP/ip) ratio. The optimized co-infection parameters were then used to generate large-scale stocks of rAAV1/AAT, which encode the human alpha-1-antitrypsin (hAAT) protein, and purified by column chromatography. The purified vector was extensively characterized by rAAV- and rHSV-specific assays and compared to transfection-made vector for in vivo efficacy in mice through intramuscular injection. The co-infection method was also used to produce rAAV9/AAT for comparison to rAAV1/AAT in vivo. Intramuscular administration of 1 x 10(11) DRP per animal of rHSV-produced rAAV1/AAT and rAAV9/AAT resulted in hAAT protein expression of 5.4 x 10(4) and 9.4 x 10(5) ng ml(-1) serum respectively, the latter being clinically relevant.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Feb
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pubmed:issn |
1476-5462
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pubmed:author | |
pubmed:issnType |
Electronic
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pubmed:volume |
16
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
229-39
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pubmed:meshHeading |
pubmed-meshheading:18923452-Animals,
pubmed-meshheading:18923452-Blotting, Western,
pubmed-meshheading:18923452-Cell Line,
pubmed-meshheading:18923452-Dependovirus,
pubmed-meshheading:18923452-Gene Transfer Techniques,
pubmed-meshheading:18923452-Genetic Vectors,
pubmed-meshheading:18923452-Herpesvirus 1, Human,
pubmed-meshheading:18923452-Humans,
pubmed-meshheading:18923452-Male,
pubmed-meshheading:18923452-Mice,
pubmed-meshheading:18923452-Mice, Inbred C57BL,
pubmed-meshheading:18923452-Recombination, Genetic,
pubmed-meshheading:18923452-Transfection,
pubmed-meshheading:18923452-Virus Cultivation,
pubmed-meshheading:18923452-alpha 1-Antitrypsin
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pubmed:year |
2009
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pubmed:articleTitle |
An efficient rHSV-based complementation system for the production of multiple rAAV vector serotypes.
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pubmed:affiliation |
Applied Genetic Technologies Corporation, Alachua, FL 32615, USA.
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pubmed:publicationType |
Journal Article
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