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Herpesvirus Vectors for Therapy of Brain Tumors

Genetically modified, conditionally-replicating Herpes Simplex Virus Type 1 (HSV-1) vectors for the treatment of malignant glioma have provided encouraging results in the handful of Phase I and Phase II clinical trials conducted to date. In recent years, a number of new strategies have been develope...

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Detalles Bibliográficos
Autores principales: Cassady, Kevin A, Parker, Jacqueline Nuss
Formato: Texto
Lenguaje:English
Publicado: Bentham Open 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2930154/
https://www.ncbi.nlm.nih.gov/pubmed/20811578
http://dx.doi.org/10.2174/1874357901004010103
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author Cassady, Kevin A
Parker, Jacqueline Nuss
author_facet Cassady, Kevin A
Parker, Jacqueline Nuss
author_sort Cassady, Kevin A
collection PubMed
description Genetically modified, conditionally-replicating Herpes Simplex Virus Type 1 (HSV-1) vectors for the treatment of malignant glioma have provided encouraging results in the handful of Phase I and Phase II clinical trials conducted to date. In recent years, a number of new strategies have been developed to improve anti-tumor activity of these attenuated vectors, through either introduction of foreign gene inserts to enhance tumor killing through a variety of mechanisms, or through combination with existing treatment regimens, including radiation and/or chemotherapeutics. Another promising new approach has been the engineering of novel oncolytic HSV vectors that retain wildtype replication, but are targeted to tumor cells through a variety of mechanisms. This review summarizes the latest advances in herpesvirus-mediated oncolytic therapies from both preclinical results and clinical trials with oncolytic HSV vectors in patients, and their implication for design of future trials.
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spelling pubmed-29301542010-09-01 Herpesvirus Vectors for Therapy of Brain Tumors Cassady, Kevin A Parker, Jacqueline Nuss Open Virol J Article Genetically modified, conditionally-replicating Herpes Simplex Virus Type 1 (HSV-1) vectors for the treatment of malignant glioma have provided encouraging results in the handful of Phase I and Phase II clinical trials conducted to date. In recent years, a number of new strategies have been developed to improve anti-tumor activity of these attenuated vectors, through either introduction of foreign gene inserts to enhance tumor killing through a variety of mechanisms, or through combination with existing treatment regimens, including radiation and/or chemotherapeutics. Another promising new approach has been the engineering of novel oncolytic HSV vectors that retain wildtype replication, but are targeted to tumor cells through a variety of mechanisms. This review summarizes the latest advances in herpesvirus-mediated oncolytic therapies from both preclinical results and clinical trials with oncolytic HSV vectors in patients, and their implication for design of future trials. Bentham Open 2010-06-18 /pmc/articles/PMC2930154/ /pubmed/20811578 http://dx.doi.org/10.2174/1874357901004010103 Text en © Cassady and Parker; Licensee Bentham Open. http: //creativecommons.org/licenses/by-nc/3.0/ This is an open access article licensed under the terms of the Creative Commons Attribution Non-Commercial License (http: //creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted, non-commercial use, distribution and reproduction in any medium, provided the work is properly cited.
spellingShingle Article
Cassady, Kevin A
Parker, Jacqueline Nuss
Herpesvirus Vectors for Therapy of Brain Tumors
title Herpesvirus Vectors for Therapy of Brain Tumors
title_full Herpesvirus Vectors for Therapy of Brain Tumors
title_fullStr Herpesvirus Vectors for Therapy of Brain Tumors
title_full_unstemmed Herpesvirus Vectors for Therapy of Brain Tumors
title_short Herpesvirus Vectors for Therapy of Brain Tumors
title_sort herpesvirus vectors for therapy of brain tumors
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2930154/
https://www.ncbi.nlm.nih.gov/pubmed/20811578
http://dx.doi.org/10.2174/1874357901004010103
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