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Antitumor Virotherapy by Attenuated Measles Virus (MV)

Antitumor virotherapy consists of the use of replication-competent viruses to infect and kill tumor cells preferentially, without damaging healthy cells. Vaccine-attenuated strains of measles virus (MV) are good candidates for this approach. Attenuated MV uses the CD46 molecule as a major entry rece...

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Autores principales: Guillerme, Jean-Baptiste, Gregoire, Marc, Tangy, Frédéric, Fonteneau, Jean-François
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3960896/
https://www.ncbi.nlm.nih.gov/pubmed/24832799
http://dx.doi.org/10.3390/biology2020587
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author Guillerme, Jean-Baptiste
Gregoire, Marc
Tangy, Frédéric
Fonteneau, Jean-François
author_facet Guillerme, Jean-Baptiste
Gregoire, Marc
Tangy, Frédéric
Fonteneau, Jean-François
author_sort Guillerme, Jean-Baptiste
collection PubMed
description Antitumor virotherapy consists of the use of replication-competent viruses to infect and kill tumor cells preferentially, without damaging healthy cells. Vaccine-attenuated strains of measles virus (MV) are good candidates for this approach. Attenuated MV uses the CD46 molecule as a major entry receptor into cells. This molecule negatively regulates the complement system and is frequently overexpressed by cancer cells to escape lysis by the complement system. MV exhibits oncolytic properties in many cancer types in vitro, and in mouse models. Phase I clinical trials using MV are currently underway. Here, we review the state of this therapeutic approach, with a focus on the effects of MV on the antitumor immune response.
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spelling pubmed-39608962014-05-07 Antitumor Virotherapy by Attenuated Measles Virus (MV) Guillerme, Jean-Baptiste Gregoire, Marc Tangy, Frédéric Fonteneau, Jean-François Biology (Basel) Review Antitumor virotherapy consists of the use of replication-competent viruses to infect and kill tumor cells preferentially, without damaging healthy cells. Vaccine-attenuated strains of measles virus (MV) are good candidates for this approach. Attenuated MV uses the CD46 molecule as a major entry receptor into cells. This molecule negatively regulates the complement system and is frequently overexpressed by cancer cells to escape lysis by the complement system. MV exhibits oncolytic properties in many cancer types in vitro, and in mouse models. Phase I clinical trials using MV are currently underway. Here, we review the state of this therapeutic approach, with a focus on the effects of MV on the antitumor immune response. MDPI 2013-03-28 /pmc/articles/PMC3960896/ /pubmed/24832799 http://dx.doi.org/10.3390/biology2020587 Text en © 2013 by the authors; licensee MDPI, Basel, Switzerland. http://creativecommons.org/licenses/by/3.0/ This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/).
spellingShingle Review
Guillerme, Jean-Baptiste
Gregoire, Marc
Tangy, Frédéric
Fonteneau, Jean-François
Antitumor Virotherapy by Attenuated Measles Virus (MV)
title Antitumor Virotherapy by Attenuated Measles Virus (MV)
title_full Antitumor Virotherapy by Attenuated Measles Virus (MV)
title_fullStr Antitumor Virotherapy by Attenuated Measles Virus (MV)
title_full_unstemmed Antitumor Virotherapy by Attenuated Measles Virus (MV)
title_short Antitumor Virotherapy by Attenuated Measles Virus (MV)
title_sort antitumor virotherapy by attenuated measles virus (mv)
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3960896/
https://www.ncbi.nlm.nih.gov/pubmed/24832799
http://dx.doi.org/10.3390/biology2020587
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