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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Main Authors: Kevin A. Cassady, Kellie B. Haworth, Josh Jackson, James M. Markert, Timothy P. Cripe
Format: Article
Language:English
Published: MDPI AG 2016-02-01
Series:Viruses
Subjects:
Online Access:http://www.mdpi.com/1999-4915/8/2/43
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spelling doaj-aab4511464bc46d2a31f932ab594d3c92020-11-24T22:52:06ZengMDPI AGViruses1999-49152016-02-01824310.3390/v8020043v8020043To Infection and Beyond: The Multi-Pronged Anti-Cancer Mechanisms of Oncolytic VirusesKevin A. Cassady0Kellie B. Haworth1Josh Jackson2James M. Markert3Timothy P. Cripe4Center for Childhood Cancer and Blood Diseases, Nationwide Children’s Hospital, The Ohio State University, 700 Children’s Drive, Columbus, OH 43205, USACenter for Childhood Cancer and Blood Diseases, Nationwide Children’s Hospital, The Ohio State University, 700 Children’s Drive, Columbus, OH 43205, USASchool of Medicine, University of Alabama-Birmingham, Birmingham, AL 35233, USADepartment of Neurosurgery, University of Alabama-Birmingham, Birmingham, AL 35233, USACenter for Childhood Cancer and Blood Diseases, Nationwide Children’s Hospital, The Ohio State University, 700 Children’s Drive, Columbus, OH 43205, USAOver 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.http://www.mdpi.com/1999-4915/8/2/43oncolytic virotherapyimmunotherapycancer
collection DOAJ
language English
format Article
sources DOAJ
author Kevin A. Cassady
Kellie B. Haworth
Josh Jackson
James M. Markert
Timothy P. Cripe
spellingShingle Kevin A. Cassady
Kellie B. Haworth
Josh Jackson
James M. Markert
Timothy P. Cripe
To Infection and Beyond: The Multi-Pronged Anti-Cancer Mechanisms of Oncolytic Viruses
Viruses
oncolytic virotherapy
immunotherapy
cancer
author_facet Kevin A. Cassady
Kellie B. Haworth
Josh Jackson
James M. Markert
Timothy P. Cripe
author_sort Kevin A. Cassady
title 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_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_sort to infection and beyond: the multi-pronged anti-cancer mechanisms of oncolytic viruses
publisher MDPI AG
series Viruses
issn 1999-4915
publishDate 2016-02-01
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.
topic oncolytic virotherapy
immunotherapy
cancer
url http://www.mdpi.com/1999-4915/8/2/43
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