Towards Clinical Implementation of Adeno-Associated Virus (AAV) Vectors for Cancer Gene Therapy: Current Status and Future Perspectives

Adeno-associated virus (AAV) vectors have gained tremendous attention as in vivo delivery systems in gene therapy for inherited monogenetic diseases. First market approvals, excellent safety data, availability of large-scale production protocols, and the possibility to tailor the vector towards opti...

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Veröffentlicht in:Cancers 2020-07, Vol.12 (7), p.1889
Hauptverfasser: Hacker, Ulrich T, Bentler, Martin, Kaniowska, Dorota, Morgan, Michael, Büning, Hildegard
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container_issue 7
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container_title Cancers
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creator Hacker, Ulrich T
Bentler, Martin
Kaniowska, Dorota
Morgan, Michael
Büning, Hildegard
description Adeno-associated virus (AAV) vectors have gained tremendous attention as in vivo delivery systems in gene therapy for inherited monogenetic diseases. First market approvals, excellent safety data, availability of large-scale production protocols, and the possibility to tailor the vector towards optimized and cell-type specific gene transfer offers to move from (ultra) rare to common diseases. Cancer, a major health burden for which novel therapeutic options are urgently needed, represents such a target. We here provide an up-to-date overview of the strategies which are currently developed for the use of AAV vectors in cancer gene therapy and discuss the perspectives for the future translation of these pre-clinical approaches into the clinic.
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subjects Cancer
Clinical trials
Disease
Expression vectors
Gene therapy
Genetic engineering
Genomes
Hemophilia
Heparan sulfate
Immunotherapy
Liver
Medical research
Metastasis
Proteins
Review
Tumors
Vectors (Biology)
Viruses
title Towards Clinical Implementation of Adeno-Associated Virus (AAV) Vectors for Cancer Gene Therapy: Current Status and Future Perspectives
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