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The Current State of Oncolytic Herpes Simplex Virus for Glioblastoma Treatment

Glioblastoma (GBM) is a lethal primary malignant brain tumor with no current effective treatments. The recent emergence of immuno-virotherapy and FDA approval of T-VEC have generated a great expectation towards oncolytic herpes simplex viruses (oHSVs) as a promising treatment option for GBM. Since t...

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Autores principales: Nguyen, Hong-My, Saha, Dipongkor
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7917312/
https://www.ncbi.nlm.nih.gov/pubmed/33659221
http://dx.doi.org/10.2147/OV.S268426
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author Nguyen, Hong-My
Saha, Dipongkor
author_facet Nguyen, Hong-My
Saha, Dipongkor
author_sort Nguyen, Hong-My
collection PubMed
description Glioblastoma (GBM) is a lethal primary malignant brain tumor with no current effective treatments. The recent emergence of immuno-virotherapy and FDA approval of T-VEC have generated a great expectation towards oncolytic herpes simplex viruses (oHSVs) as a promising treatment option for GBM. Since the generation and testing of the first genetically engineered oHSV in glioma in the early 1990s, oHSV-based therapies have shown a long way of great progress in terms of anti-GBM efficacy and safety, both preclinically and clinically. Here, we revisit the literature to understand the recent advancement of oHSV in the treatment of GBM. In addition, we discuss current obstacles to oHSV-based therapies and possible strategies to overcome these pitfalls.
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spelling pubmed-79173122021-03-02 The Current State of Oncolytic Herpes Simplex Virus for Glioblastoma Treatment Nguyen, Hong-My Saha, Dipongkor Oncolytic Virother Review Glioblastoma (GBM) is a lethal primary malignant brain tumor with no current effective treatments. The recent emergence of immuno-virotherapy and FDA approval of T-VEC have generated a great expectation towards oncolytic herpes simplex viruses (oHSVs) as a promising treatment option for GBM. Since the generation and testing of the first genetically engineered oHSV in glioma in the early 1990s, oHSV-based therapies have shown a long way of great progress in terms of anti-GBM efficacy and safety, both preclinically and clinically. Here, we revisit the literature to understand the recent advancement of oHSV in the treatment of GBM. In addition, we discuss current obstacles to oHSV-based therapies and possible strategies to overcome these pitfalls. Dove 2021-02-24 /pmc/articles/PMC7917312/ /pubmed/33659221 http://dx.doi.org/10.2147/OV.S268426 Text en © 2021 Nguyen and Saha. http://creativecommons.org/licenses/by-nc/3.0/ This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php).
spellingShingle Review
Nguyen, Hong-My
Saha, Dipongkor
The Current State of Oncolytic Herpes Simplex Virus for Glioblastoma Treatment
title The Current State of Oncolytic Herpes Simplex Virus for Glioblastoma Treatment
title_full The Current State of Oncolytic Herpes Simplex Virus for Glioblastoma Treatment
title_fullStr The Current State of Oncolytic Herpes Simplex Virus for Glioblastoma Treatment
title_full_unstemmed The Current State of Oncolytic Herpes Simplex Virus for Glioblastoma Treatment
title_short The Current State of Oncolytic Herpes Simplex Virus for Glioblastoma Treatment
title_sort current state of oncolytic herpes simplex virus for glioblastoma treatment
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7917312/
https://www.ncbi.nlm.nih.gov/pubmed/33659221
http://dx.doi.org/10.2147/OV.S268426
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