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Newcastle Disease Virus: Potential Therapeutic Application for Human and Canine Lymphoma

Research on oncolytic viruses has mostly been directed towards the treatment of solid tumors, which has yielded limited information regarding their activity in hematological cancer. It has also been directed towards the treatment of humans, yet veterinary medicine may also benefit. Several strains o...

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Autores principales: Sánchez, Diana, Pelayo, Rosana, Medina, Luis Alberto, Vadillo, Eduardo, Sánchez, Rogelio, Núñez, Luis, Cesarman-Maus, Gabriela, Sarmiento-Silva, Rosa Elena
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4728563/
https://www.ncbi.nlm.nih.gov/pubmed/26703717
http://dx.doi.org/10.3390/v8010003
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author Sánchez, Diana
Pelayo, Rosana
Medina, Luis Alberto
Vadillo, Eduardo
Sánchez, Rogelio
Núñez, Luis
Cesarman-Maus, Gabriela
Sarmiento-Silva, Rosa Elena
author_facet Sánchez, Diana
Pelayo, Rosana
Medina, Luis Alberto
Vadillo, Eduardo
Sánchez, Rogelio
Núñez, Luis
Cesarman-Maus, Gabriela
Sarmiento-Silva, Rosa Elena
author_sort Sánchez, Diana
collection PubMed
description Research on oncolytic viruses has mostly been directed towards the treatment of solid tumors, which has yielded limited information regarding their activity in hematological cancer. It has also been directed towards the treatment of humans, yet veterinary medicine may also benefit. Several strains of the Newcastle disease virus (NDV) have been used as oncolytics in vitro and in a number of in vivo experiments. We studied the cytolytic effect of NDV-MLS, a low virulence attenuated lentogenic strain, on a human large B-cell lymphoma cell line (SU-DHL-4), as well as on primary canine-derived B-cell lymphoma cells, and compared them to healthy peripheral blood mononuclear cells (PBMC) from both humans and dogs. NDV-MLS reduced cell survival in both human (42% ± 5%) and dog (34% ± 12%) lymphoma cells as compared to untreated controls. No significant effect on PBMC was seen. Cell death involved apoptosis as documented by flow-cytometry. NDV-MLS infections of malignant lymphoma tumors in vivo in dogs were confirmed by electron microscopy. Early (24 h) biodistribution of intravenous injection of 1 × 10(12) TCID(50) (tissue culture infective dose) in a dog with T-cell lymphoma showed viral localization only in the kidney, the salivary gland, the lung and the stomach by immunohistochemistry and/or endpoint PCR. We conclude that NDV-MLS may be a promising agent for the treatment of lymphomas. Future research is needed to elucidate the optimal therapeutic regimen and establish appropriate biosafety measures.
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spelling pubmed-47285632016-02-08 Newcastle Disease Virus: Potential Therapeutic Application for Human and Canine Lymphoma Sánchez, Diana Pelayo, Rosana Medina, Luis Alberto Vadillo, Eduardo Sánchez, Rogelio Núñez, Luis Cesarman-Maus, Gabriela Sarmiento-Silva, Rosa Elena Viruses Article Research on oncolytic viruses has mostly been directed towards the treatment of solid tumors, which has yielded limited information regarding their activity in hematological cancer. It has also been directed towards the treatment of humans, yet veterinary medicine may also benefit. Several strains of the Newcastle disease virus (NDV) have been used as oncolytics in vitro and in a number of in vivo experiments. We studied the cytolytic effect of NDV-MLS, a low virulence attenuated lentogenic strain, on a human large B-cell lymphoma cell line (SU-DHL-4), as well as on primary canine-derived B-cell lymphoma cells, and compared them to healthy peripheral blood mononuclear cells (PBMC) from both humans and dogs. NDV-MLS reduced cell survival in both human (42% ± 5%) and dog (34% ± 12%) lymphoma cells as compared to untreated controls. No significant effect on PBMC was seen. Cell death involved apoptosis as documented by flow-cytometry. NDV-MLS infections of malignant lymphoma tumors in vivo in dogs were confirmed by electron microscopy. Early (24 h) biodistribution of intravenous injection of 1 × 10(12) TCID(50) (tissue culture infective dose) in a dog with T-cell lymphoma showed viral localization only in the kidney, the salivary gland, the lung and the stomach by immunohistochemistry and/or endpoint PCR. We conclude that NDV-MLS may be a promising agent for the treatment of lymphomas. Future research is needed to elucidate the optimal therapeutic regimen and establish appropriate biosafety measures. MDPI 2015-12-23 /pmc/articles/PMC4728563/ /pubmed/26703717 http://dx.doi.org/10.3390/v8010003 Text en © 2015 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 Article
Sánchez, Diana
Pelayo, Rosana
Medina, Luis Alberto
Vadillo, Eduardo
Sánchez, Rogelio
Núñez, Luis
Cesarman-Maus, Gabriela
Sarmiento-Silva, Rosa Elena
Newcastle Disease Virus: Potential Therapeutic Application for Human and Canine Lymphoma
title Newcastle Disease Virus: Potential Therapeutic Application for Human and Canine Lymphoma
title_full Newcastle Disease Virus: Potential Therapeutic Application for Human and Canine Lymphoma
title_fullStr Newcastle Disease Virus: Potential Therapeutic Application for Human and Canine Lymphoma
title_full_unstemmed Newcastle Disease Virus: Potential Therapeutic Application for Human and Canine Lymphoma
title_short Newcastle Disease Virus: Potential Therapeutic Application for Human and Canine Lymphoma
title_sort newcastle disease virus: potential therapeutic application for human and canine lymphoma
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4728563/
https://www.ncbi.nlm.nih.gov/pubmed/26703717
http://dx.doi.org/10.3390/v8010003
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