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Replicating viral vectors for cancer therapy: strategies to synergize with host immune responses

Tumour‐specific replicating (oncolytic) viruses are novel anticancer agents, currently under intense investigation in preclinical studies and phase I–III clinical trials. Until recently, most studies have focused on the direct antitumour properties of these viruses. There is now an increasing body o...

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Detalles Bibliográficos
Autores principales: Altomonte, Jennifer, Ebert, Oliver
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Blackwell Publishing Ltd 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3815785/
https://www.ncbi.nlm.nih.gov/pubmed/21923638
http://dx.doi.org/10.1111/j.1751-7915.2011.00296.x
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author Altomonte, Jennifer
Ebert, Oliver
author_facet Altomonte, Jennifer
Ebert, Oliver
author_sort Altomonte, Jennifer
collection PubMed
description Tumour‐specific replicating (oncolytic) viruses are novel anticancer agents, currently under intense investigation in preclinical studies and phase I–III clinical trials. Until recently, most studies have focused on the direct antitumour properties of these viruses. There is now an increasing body of evidence indicating that host immune responses may be critical to the efficacy of oncolytic virotherapy. Although the immune response to oncolytic viruses can rapidly restrict viral replication, thereby limiting the efficacy of therapy, oncolytic virotherapy also has the potential to induce potent antitumoural immune effectors that destroy those cancer cells, which are not directly lysed by virus. In this review, we discuss the role of the immune system in terms of antiviral and antitumoural responses, as well as strategies to evade or promote these responses in favour of improved therapeutic potentials.
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spelling pubmed-38157852014-02-12 Replicating viral vectors for cancer therapy: strategies to synergize with host immune responses Altomonte, Jennifer Ebert, Oliver Microb Biotechnol Research Articles Tumour‐specific replicating (oncolytic) viruses are novel anticancer agents, currently under intense investigation in preclinical studies and phase I–III clinical trials. Until recently, most studies have focused on the direct antitumour properties of these viruses. There is now an increasing body of evidence indicating that host immune responses may be critical to the efficacy of oncolytic virotherapy. Although the immune response to oncolytic viruses can rapidly restrict viral replication, thereby limiting the efficacy of therapy, oncolytic virotherapy also has the potential to induce potent antitumoural immune effectors that destroy those cancer cells, which are not directly lysed by virus. In this review, we discuss the role of the immune system in terms of antiviral and antitumoural responses, as well as strategies to evade or promote these responses in favour of improved therapeutic potentials. Blackwell Publishing Ltd 2012-03 2012-02-20 /pmc/articles/PMC3815785/ /pubmed/21923638 http://dx.doi.org/10.1111/j.1751-7915.2011.00296.x Text en Copyright © 2011 The Authors. Microbial Biotechnology © 2011 Society for Applied Microbiology and Blackwell Publishing Ltd
spellingShingle Research Articles
Altomonte, Jennifer
Ebert, Oliver
Replicating viral vectors for cancer therapy: strategies to synergize with host immune responses
title Replicating viral vectors for cancer therapy: strategies to synergize with host immune responses
title_full Replicating viral vectors for cancer therapy: strategies to synergize with host immune responses
title_fullStr Replicating viral vectors for cancer therapy: strategies to synergize with host immune responses
title_full_unstemmed Replicating viral vectors for cancer therapy: strategies to synergize with host immune responses
title_short Replicating viral vectors for cancer therapy: strategies to synergize with host immune responses
title_sort replicating viral vectors for cancer therapy: strategies to synergize with host immune responses
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3815785/
https://www.ncbi.nlm.nih.gov/pubmed/21923638
http://dx.doi.org/10.1111/j.1751-7915.2011.00296.x
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