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H-1 Parvovirus as a Cancer-Killing Agent: Past, Present, and Future

The rat protoparvovirus H-1PV is nonpathogenic in humans, replicates preferentially in cancer cells, and has natural oncolytic and oncosuppressive activities. The virus is able to kill cancer cells by activating several cell death pathways. H-1PV-mediated cancer cell death is often immunogenic and t...

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Detalles Bibliográficos
Autores principales: Bretscher, Clemens, Marchini, Antonio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6630270/
https://www.ncbi.nlm.nih.gov/pubmed/31216641
http://dx.doi.org/10.3390/v11060562
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author Bretscher, Clemens
Marchini, Antonio
author_facet Bretscher, Clemens
Marchini, Antonio
author_sort Bretscher, Clemens
collection PubMed
description The rat protoparvovirus H-1PV is nonpathogenic in humans, replicates preferentially in cancer cells, and has natural oncolytic and oncosuppressive activities. The virus is able to kill cancer cells by activating several cell death pathways. H-1PV-mediated cancer cell death is often immunogenic and triggers anticancer immune responses. The safety and tolerability of H-1PV treatment has been demonstrated in early clinical studies in glioma and pancreatic carcinoma patients. Virus treatment was associated with surrogate signs of efficacy including immune conversion of tumor microenvironment, effective virus distribution into the tumor bed even after systemic administration, and improved patient overall survival compared with historical control. However, monotherapeutic use of the virus was unable to eradicate tumors. Thus, further studies are needed to improve H-1PV’s anticancer profile. In this review, we describe H-1PV’s anticancer properties and discuss recent efforts to improve the efficacy of H-1PV and, thereby, the clinical outcome of H-1PV-based therapies.
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spelling pubmed-66302702019-08-19 H-1 Parvovirus as a Cancer-Killing Agent: Past, Present, and Future Bretscher, Clemens Marchini, Antonio Viruses Review The rat protoparvovirus H-1PV is nonpathogenic in humans, replicates preferentially in cancer cells, and has natural oncolytic and oncosuppressive activities. The virus is able to kill cancer cells by activating several cell death pathways. H-1PV-mediated cancer cell death is often immunogenic and triggers anticancer immune responses. The safety and tolerability of H-1PV treatment has been demonstrated in early clinical studies in glioma and pancreatic carcinoma patients. Virus treatment was associated with surrogate signs of efficacy including immune conversion of tumor microenvironment, effective virus distribution into the tumor bed even after systemic administration, and improved patient overall survival compared with historical control. However, monotherapeutic use of the virus was unable to eradicate tumors. Thus, further studies are needed to improve H-1PV’s anticancer profile. In this review, we describe H-1PV’s anticancer properties and discuss recent efforts to improve the efficacy of H-1PV and, thereby, the clinical outcome of H-1PV-based therapies. MDPI 2019-06-18 /pmc/articles/PMC6630270/ /pubmed/31216641 http://dx.doi.org/10.3390/v11060562 Text en © 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Bretscher, Clemens
Marchini, Antonio
H-1 Parvovirus as a Cancer-Killing Agent: Past, Present, and Future
title H-1 Parvovirus as a Cancer-Killing Agent: Past, Present, and Future
title_full H-1 Parvovirus as a Cancer-Killing Agent: Past, Present, and Future
title_fullStr H-1 Parvovirus as a Cancer-Killing Agent: Past, Present, and Future
title_full_unstemmed H-1 Parvovirus as a Cancer-Killing Agent: Past, Present, and Future
title_short H-1 Parvovirus as a Cancer-Killing Agent: Past, Present, and Future
title_sort h-1 parvovirus as a cancer-killing agent: past, present, and future
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6630270/
https://www.ncbi.nlm.nih.gov/pubmed/31216641
http://dx.doi.org/10.3390/v11060562
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