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Pharmacological Modulation of Anti-Tumor Immunity Induced by Oncolytic Viruses

Oncolytic viruses (OVs) not only kill cancer cells by direct lysis but also generate a significant anti-tumor immune response that allows for prolonged cancer control and in some cases cures. How to best stimulate this effect is a subject of intense investigation in the OV field. While pharmacologic...

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Autores principales: Forbes, Nicole E., Krishnan, Ramya, Diallo, Jean-Simon
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4108035/
https://www.ncbi.nlm.nih.gov/pubmed/25101247
http://dx.doi.org/10.3389/fonc.2014.00191
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author Forbes, Nicole E.
Krishnan, Ramya
Diallo, Jean-Simon
author_facet Forbes, Nicole E.
Krishnan, Ramya
Diallo, Jean-Simon
author_sort Forbes, Nicole E.
collection PubMed
description Oncolytic viruses (OVs) not only kill cancer cells by direct lysis but also generate a significant anti-tumor immune response that allows for prolonged cancer control and in some cases cures. How to best stimulate this effect is a subject of intense investigation in the OV field. While pharmacological manipulation of the cellular innate anti-viral immune response has been shown by several groups to improve viral oncolysis and spread, it is increasingly clear that pharmacological agents can also impact the anti-tumor immune response generated by OVs and related tumor vaccination strategies. This review covers recent progress in using pharmacological agents to improve the activity of OVs and their ability to generate robust anti-tumor immune responses.
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spelling pubmed-41080352014-08-06 Pharmacological Modulation of Anti-Tumor Immunity Induced by Oncolytic Viruses Forbes, Nicole E. Krishnan, Ramya Diallo, Jean-Simon Front Oncol Oncology Oncolytic viruses (OVs) not only kill cancer cells by direct lysis but also generate a significant anti-tumor immune response that allows for prolonged cancer control and in some cases cures. How to best stimulate this effect is a subject of intense investigation in the OV field. While pharmacological manipulation of the cellular innate anti-viral immune response has been shown by several groups to improve viral oncolysis and spread, it is increasingly clear that pharmacological agents can also impact the anti-tumor immune response generated by OVs and related tumor vaccination strategies. This review covers recent progress in using pharmacological agents to improve the activity of OVs and their ability to generate robust anti-tumor immune responses. Frontiers Media S.A. 2014-07-23 /pmc/articles/PMC4108035/ /pubmed/25101247 http://dx.doi.org/10.3389/fonc.2014.00191 Text en Copyright © 2014 Forbes, Krishnan and Diallo. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Oncology
Forbes, Nicole E.
Krishnan, Ramya
Diallo, Jean-Simon
Pharmacological Modulation of Anti-Tumor Immunity Induced by Oncolytic Viruses
title Pharmacological Modulation of Anti-Tumor Immunity Induced by Oncolytic Viruses
title_full Pharmacological Modulation of Anti-Tumor Immunity Induced by Oncolytic Viruses
title_fullStr Pharmacological Modulation of Anti-Tumor Immunity Induced by Oncolytic Viruses
title_full_unstemmed Pharmacological Modulation of Anti-Tumor Immunity Induced by Oncolytic Viruses
title_short Pharmacological Modulation of Anti-Tumor Immunity Induced by Oncolytic Viruses
title_sort pharmacological modulation of anti-tumor immunity induced by oncolytic viruses
topic Oncology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4108035/
https://www.ncbi.nlm.nih.gov/pubmed/25101247
http://dx.doi.org/10.3389/fonc.2014.00191
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