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Insulators to Improve the Safety of Retroviral Vectors for HIV Gene Therapy

Retroviral vector gene therapy is a promising approach to treating HIV-1. However, integrated vectors are mutagens with the potential to dysregulate nearby genes and cause severe adverse side effects. Leukemia has already been a documented severe adverse event in gene therapy clinical trials for the...

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Autores principales: Browning, Diana L., Trobridge, Grant D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5344246/
https://www.ncbi.nlm.nih.gov/pubmed/28424756
http://dx.doi.org/10.3390/biomedicines4010004
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author Browning, Diana L.
Trobridge, Grant D.
author_facet Browning, Diana L.
Trobridge, Grant D.
author_sort Browning, Diana L.
collection PubMed
description Retroviral vector gene therapy is a promising approach to treating HIV-1. However, integrated vectors are mutagens with the potential to dysregulate nearby genes and cause severe adverse side effects. Leukemia has already been a documented severe adverse event in gene therapy clinical trials for the treatment of primary immunodeficiencies. These side effects will need to be reduced or avoided if retroviral vectors are to be used clinically for HIV-1 treatment. The addition of chromatin insulators to retroviral vectors is a potential strategy for reducing adverse side effects. Insulators have already been effectively used in retroviral vectors to reduce genotoxicity in pre-clinical studies. Here, we will review how insulators function, genotoxicity in gene therapy clinical trials, the design of insulated retroviral vectors, promising results from insulated retroviral vector studies, and considerations for the development of insulated retroviral treatment vectors for HIV-1 gene therapy.
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spelling pubmed-53442462017-04-17 Insulators to Improve the Safety of Retroviral Vectors for HIV Gene Therapy Browning, Diana L. Trobridge, Grant D. Biomedicines Review Retroviral vector gene therapy is a promising approach to treating HIV-1. However, integrated vectors are mutagens with the potential to dysregulate nearby genes and cause severe adverse side effects. Leukemia has already been a documented severe adverse event in gene therapy clinical trials for the treatment of primary immunodeficiencies. These side effects will need to be reduced or avoided if retroviral vectors are to be used clinically for HIV-1 treatment. The addition of chromatin insulators to retroviral vectors is a potential strategy for reducing adverse side effects. Insulators have already been effectively used in retroviral vectors to reduce genotoxicity in pre-clinical studies. Here, we will review how insulators function, genotoxicity in gene therapy clinical trials, the design of insulated retroviral vectors, promising results from insulated retroviral vector studies, and considerations for the development of insulated retroviral treatment vectors for HIV-1 gene therapy. MDPI 2016-02-02 /pmc/articles/PMC5344246/ /pubmed/28424756 http://dx.doi.org/10.3390/biomedicines4010004 Text en © 2015 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons by Attribution (CC-BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Browning, Diana L.
Trobridge, Grant D.
Insulators to Improve the Safety of Retroviral Vectors for HIV Gene Therapy
title Insulators to Improve the Safety of Retroviral Vectors for HIV Gene Therapy
title_full Insulators to Improve the Safety of Retroviral Vectors for HIV Gene Therapy
title_fullStr Insulators to Improve the Safety of Retroviral Vectors for HIV Gene Therapy
title_full_unstemmed Insulators to Improve the Safety of Retroviral Vectors for HIV Gene Therapy
title_short Insulators to Improve the Safety of Retroviral Vectors for HIV Gene Therapy
title_sort insulators to improve the safety of retroviral vectors for hiv gene therapy
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5344246/
https://www.ncbi.nlm.nih.gov/pubmed/28424756
http://dx.doi.org/10.3390/biomedicines4010004
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