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Adeno-associated virus (AAV) vectors in cancer gene therapy.

Jorge L Santiago-Ortiz·David V Schaffer
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Abstract

Gene delivery vectors based on adeno-associated virus (AAV) have been utilized in a large number of gene therapy clinical trials, which have demonstrated their strong safety profile and increasingly their therapeutic efficacy for treating monogenic diseases. For cancer applications, AAV vectors have been harnessed for delivery of an extensive repertoire of transgenes to preclinical models and, more recently, clinical trials involving certain cancers. This review describes the applications of AAV vectors to cancer models and presents developments in vector engineering and payload design aimed at tailoring AAV vectors for transduction and treatment of cancer cells. We also discuss the current status of AAV clinical development in oncology and future directions for AAV in this field.

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Capsid ProteinsClinical Trials as TopicDependovirusGene Transfer TechniquesGenetic TherapyGenetic VectorsHumansNeoplasmsProtein EngineeringTransgenesAAVAdeno-associated virusCancerGene deliveryGene delivery vectorsGene therapyJournal ArticleReviewResearch Support, N.I.H., ExtramuralResearch Support, U.S. Gov't, Non-P.H.S.Research Support, Non-U.S. Gov't

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Jorge L Santiago-Ortiz, David V Schaffer. 2016-01-12. Adeno-associated virus (AAV) vectors in cancer gene therapy.. https://doi.org/10.1016/j.jconrel.2016.01.001

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