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Aurintricarboxylic acid increases yield of HSV-1 vectors
Author(s) -
Peter Pecháň,
Jeffery Ardinger,
Jyothi Ketavarapu,
Hillard Rubin,
Samuel C. Wadsworth,
Abraham Scaria
Publication year - 2014
Publication title -
molecular therapy — methods and clinical development
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.285
H-Index - 32
ISSN - 2329-0501
DOI - 10.1038/mtm.2013.6
Subject(s) - aurintricarboxylic acid , herpes simplex virus , virology , vector (molecular biology) , titer , virus , dexamethasone , hsl and hsv , biology , recombinant dna , gene , apoptosis , biochemistry , endocrinology , programmed cell death
Production of large quantities of viral vectors is crucial for the success of gene therapy in the clinic. There is a need for higher titers of herpes simplex virus-1 (HSV-1) vectors both for therapeutic use as well as in the manufacturing of clinical grade adeno-associated virus (AAV) vectors. HSV-1 yield increased when primary human fibroblasts were treated with anti-inflammatory drugs like dexamethasone or valproic acid. In our search for compounds that would increase HSV-1 yield, we investigated another anti-inflammatory compound, aurintricarboxylic acid (ATA). Although ATA has been previously shown to have antiviral effects, we find that low (micromolar) concentrations of ATA increased HSV-1 vector production yields. Our results showing the use of ATA to increase HSV-1 titers have important implications for the production of certain HSV-1 vectors as well as recombinant AAV vectors

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