In vivo Gene Therapy to the Liver and Nervous System: Promises and Challenges

In vivo genetic engineering has recently shown remarkable potential as a novel effective treatment for an ever-growing number of diseases, as also witnessed by the recent marketing authorization of several in vivo gene therapy products. In vivo genetic engineering comprises both viral vector-mediate...

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Published inFrontiers in medicine Vol. 8; p. 774618
Main Authors Cantore, Alessio, Fraldi, Alessandro, Meneghini, Vasco, Gritti, Angela
Format Journal Article
LanguageEnglish
Published Switzerland Frontiers Media S.A 18.01.2022
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ISSN2296-858X
2296-858X
DOI10.3389/fmed.2021.774618

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Summary:In vivo genetic engineering has recently shown remarkable potential as a novel effective treatment for an ever-growing number of diseases, as also witnessed by the recent marketing authorization of several in vivo gene therapy products. In vivo genetic engineering comprises both viral vector-mediated gene transfer and the more recently developed genome/epigenome editing strategies, as long as they are directly administered to patients. Here we first review the most advanced in vivo gene therapies that are commercially available or in clinical development. We then highlight the major challenges to be overcome to fully and broadly exploit in vivo gene therapies as novel medicines, discussing some of the approaches that are being taken to address them, with a focus on the nervous system and liver taken as paradigmatic examples.
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Reviewed by: Haihui Pan, George Washington University, United States; Hai Bac Tran, University of Adelaide, Australia
Edited by: Nuno M. Neves, University of Minho, Portugal
This article was submitted to Translational Medicine, a section of the journal Frontiers in Medicine
ISSN:2296-858X
2296-858X
DOI:10.3389/fmed.2021.774618