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 in | Frontiers in medicine Vol. 8; p. 774618 |
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Main Authors | , , , |
Format | Journal Article |
Language | English |
Published |
Switzerland
Frontiers Media S.A
18.01.2022
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Subjects | |
Online Access | Get full text |
ISSN | 2296-858X 2296-858X |
DOI | 10.3389/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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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 ObjectType-Review-3 content type line 23 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 |