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Association Between Simian Virus 40 and Human Tumors

Simian virus 40 (SV40) is a small DNA tumor virus of monkey origin. This polyomavirus was administered to human populations mainly through contaminated polio vaccines, which were produced in naturally infected SV40 monkey cells. Previous molecular biology and recent immunological assays have indicat...

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Autores principales: Rotondo, John Charles, Mazzoni, Elisa, Bononi, Ilaria, Tognon, Mauro, Martini, Fernanda
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6669359/
https://www.ncbi.nlm.nih.gov/pubmed/31403031
http://dx.doi.org/10.3389/fonc.2019.00670
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author Rotondo, John Charles
Mazzoni, Elisa
Bononi, Ilaria
Tognon, Mauro
Martini, Fernanda
author_facet Rotondo, John Charles
Mazzoni, Elisa
Bononi, Ilaria
Tognon, Mauro
Martini, Fernanda
author_sort Rotondo, John Charles
collection PubMed
description Simian virus 40 (SV40) is a small DNA tumor virus of monkey origin. This polyomavirus was administered to human populations mainly through contaminated polio vaccines, which were produced in naturally infected SV40 monkey cells. Previous molecular biology and recent immunological assays have indicated that SV40 is spreading in human populations, independently from earlier SV40-contaminated vaccines. SV40 DNA sequences have been detected at a higher prevalence in specific human cancer specimens, such as the brain and bone tumors, malignant pleural mesotheliomas, and lymphoproliferative disorders, compared to the corresponding normal tissues/specimens. However, other investigations, which reported negative data, did not confirm an association between SV40 and human tumors. To circumvent the controversies, which have arisen because of these molecular biology studies, immunological researches with newly developed indirect ELISA tests were carried out in serum samples from patients affected by the same kind of tumors as mentioned above. These innovative indirect ELISAs employ synthetic peptides as mimotopes/specific SV40 antigens. SV40 mimotopes do not cross-react with the homologous human polyomaviruses, BKPyV, and JCPyV. Immunological data obtained from indirect ELISAs, using SV40 mimotopes, employed to analyze serum samples from oncological patients, have indicated that these sera had a higher prevalence of antibodies against SV40 compared to healthy subjects. The main data on (i) the biology and genetics of SV40; (ii) the epidemiology of SV40 in the general population, (iii) the mechanisms of SV40 transformation; (iv) the putative role of SV40 in the onset/progression of specific human tumors, and (v) its association with other human diseases are reported in this review.
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spelling pubmed-66693592019-08-09 Association Between Simian Virus 40 and Human Tumors Rotondo, John Charles Mazzoni, Elisa Bononi, Ilaria Tognon, Mauro Martini, Fernanda Front Oncol Oncology Simian virus 40 (SV40) is a small DNA tumor virus of monkey origin. This polyomavirus was administered to human populations mainly through contaminated polio vaccines, which were produced in naturally infected SV40 monkey cells. Previous molecular biology and recent immunological assays have indicated that SV40 is spreading in human populations, independently from earlier SV40-contaminated vaccines. SV40 DNA sequences have been detected at a higher prevalence in specific human cancer specimens, such as the brain and bone tumors, malignant pleural mesotheliomas, and lymphoproliferative disorders, compared to the corresponding normal tissues/specimens. However, other investigations, which reported negative data, did not confirm an association between SV40 and human tumors. To circumvent the controversies, which have arisen because of these molecular biology studies, immunological researches with newly developed indirect ELISA tests were carried out in serum samples from patients affected by the same kind of tumors as mentioned above. These innovative indirect ELISAs employ synthetic peptides as mimotopes/specific SV40 antigens. SV40 mimotopes do not cross-react with the homologous human polyomaviruses, BKPyV, and JCPyV. Immunological data obtained from indirect ELISAs, using SV40 mimotopes, employed to analyze serum samples from oncological patients, have indicated that these sera had a higher prevalence of antibodies against SV40 compared to healthy subjects. The main data on (i) the biology and genetics of SV40; (ii) the epidemiology of SV40 in the general population, (iii) the mechanisms of SV40 transformation; (iv) the putative role of SV40 in the onset/progression of specific human tumors, and (v) its association with other human diseases are reported in this review. Frontiers Media S.A. 2019-07-25 /pmc/articles/PMC6669359/ /pubmed/31403031 http://dx.doi.org/10.3389/fonc.2019.00670 Text en Copyright © 2019 Rotondo, Mazzoni, Bononi, Tognon and Martini. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Oncology
Rotondo, John Charles
Mazzoni, Elisa
Bononi, Ilaria
Tognon, Mauro
Martini, Fernanda
Association Between Simian Virus 40 and Human Tumors
title Association Between Simian Virus 40 and Human Tumors
title_full Association Between Simian Virus 40 and Human Tumors
title_fullStr Association Between Simian Virus 40 and Human Tumors
title_full_unstemmed Association Between Simian Virus 40 and Human Tumors
title_short Association Between Simian Virus 40 and Human Tumors
title_sort association between simian virus 40 and human tumors
topic Oncology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6669359/
https://www.ncbi.nlm.nih.gov/pubmed/31403031
http://dx.doi.org/10.3389/fonc.2019.00670
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