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To Infection and Beyond: The Multi-Pronged Anti-Cancer Mechanisms of Oncolytic Viruses

Over the past 1–2 decades we have witnessed a resurgence of efforts to therapeutically exploit the attributes of lytic viruses to infect and kill tumor cells while sparing normal cells. We now appreciate that the utility of viruses for treating cancer extends far beyond lytic cell death. Viruses are...

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Autores principales: Cassady, Kevin A., Haworth, Kellie B., Jackson, Josh, Markert, James M., Cripe, Timothy P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4776198/
https://www.ncbi.nlm.nih.gov/pubmed/26861381
http://dx.doi.org/10.3390/v8020043
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author Cassady, Kevin A.
Haworth, Kellie B.
Jackson, Josh
Markert, James M.
Cripe, Timothy P.
author_facet Cassady, Kevin A.
Haworth, Kellie B.
Jackson, Josh
Markert, James M.
Cripe, Timothy P.
author_sort Cassady, Kevin A.
collection PubMed
description Over the past 1–2 decades we have witnessed a resurgence of efforts to therapeutically exploit the attributes of lytic viruses to infect and kill tumor cells while sparing normal cells. We now appreciate that the utility of viruses for treating cancer extends far beyond lytic cell death. Viruses are also capable of eliciting humoral and cellular innate and adaptive immune responses that may be directed not only at virus-infected cells but also at uninfected cancer cells. Here we review our current understanding of this bystander effect, and divide the mechanisms into lytic, cytokine, innate cellular, and adaptive phases. Knowing the key pathways and molecular players during virus infection in the context of the cancer microenvironment will be critical to devise strategies to maximize the therapeutic effects of oncolytic viroimmunotherapy.
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spelling pubmed-47761982016-03-09 To Infection and Beyond: The Multi-Pronged Anti-Cancer Mechanisms of Oncolytic Viruses Cassady, Kevin A. Haworth, Kellie B. Jackson, Josh Markert, James M. Cripe, Timothy P. Viruses Review Over the past 1–2 decades we have witnessed a resurgence of efforts to therapeutically exploit the attributes of lytic viruses to infect and kill tumor cells while sparing normal cells. We now appreciate that the utility of viruses for treating cancer extends far beyond lytic cell death. Viruses are also capable of eliciting humoral and cellular innate and adaptive immune responses that may be directed not only at virus-infected cells but also at uninfected cancer cells. Here we review our current understanding of this bystander effect, and divide the mechanisms into lytic, cytokine, innate cellular, and adaptive phases. Knowing the key pathways and molecular players during virus infection in the context of the cancer microenvironment will be critical to devise strategies to maximize the therapeutic effects of oncolytic viroimmunotherapy. MDPI 2016-02-04 /pmc/articles/PMC4776198/ /pubmed/26861381 http://dx.doi.org/10.3390/v8020043 Text en © 2016 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
Cassady, Kevin A.
Haworth, Kellie B.
Jackson, Josh
Markert, James M.
Cripe, Timothy P.
To Infection and Beyond: The Multi-Pronged Anti-Cancer Mechanisms of Oncolytic Viruses
title To Infection and Beyond: The Multi-Pronged Anti-Cancer Mechanisms of Oncolytic Viruses
title_full To Infection and Beyond: The Multi-Pronged Anti-Cancer Mechanisms of Oncolytic Viruses
title_fullStr To Infection and Beyond: The Multi-Pronged Anti-Cancer Mechanisms of Oncolytic Viruses
title_full_unstemmed To Infection and Beyond: The Multi-Pronged Anti-Cancer Mechanisms of Oncolytic Viruses
title_short To Infection and Beyond: The Multi-Pronged Anti-Cancer Mechanisms of Oncolytic Viruses
title_sort to infection and beyond: the multi-pronged anti-cancer mechanisms of oncolytic viruses
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4776198/
https://www.ncbi.nlm.nih.gov/pubmed/26861381
http://dx.doi.org/10.3390/v8020043
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