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Human polyomavirus BKPyV and JCPyV serostatus has no impact on women´s human papillomavirus infection outcome
INTRODUCTION: Polyomaviruses have both structural and functional similarities with papillomaviruses. Accordingly, their role in human papillomavirus (HPV) associated malignancies has been studied with conflicting results. Our goal was to disclose any association between BK (BKPyV) and/or JC (JCPyV)...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2023
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10272380/ https://www.ncbi.nlm.nih.gov/pubmed/37333846 http://dx.doi.org/10.3389/fcimb.2023.1190019 |
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author | Laine, Hanna K. Waterboer, Tim Syrjänen, Kari Grenman, Seija Louvanto, Karolina Syrjänen, Stina |
author_facet | Laine, Hanna K. Waterboer, Tim Syrjänen, Kari Grenman, Seija Louvanto, Karolina Syrjänen, Stina |
author_sort | Laine, Hanna K. |
collection | PubMed |
description | INTRODUCTION: Polyomaviruses have both structural and functional similarities with papillomaviruses. Accordingly, their role in human papillomavirus (HPV) associated malignancies has been studied with conflicting results. Our goal was to disclose any association between BK (BKPyV) and/or JC (JCPyV) polyomavirus serology and HPV data derived from Finnish women (327) in a 6-year prospective follow-up. METHODS: Glutathione S-transferase fusion-protein-capture (ELISA) in combination with fluorescent bead technology was used to analyze antibodies to BKPyV and JCPyV. In the longitudinal setting, BKPyV or JCPyV serostatus was related to i) oral- and ii) genital low (LR)- and high risk (HR) HPV DNA detection, iii) HPV16 persistence at both these sites, iv) results of the Pap (Papanicolaou) smear taken at baseline, and v) development of incident CIN (cervical intraepithelial neoplasia) during the follow-up. RESULTS: Being BKPyV or JCPyV seropositive was not significantly associated with HPV seropositivity to either LR- or HR-genotypes, genital- or oral HPV DNA positivity, persistence of genital- or oral HPV16 infection, grade of Pap smear, or development of incident CIN. DISCUSSION: Thus, the present study could not provide any confirmation to the concept that co-infections by HPyV and HPV have interactions that impact on the clinical manifestations or outcomes of HPV infections either in the genital tract or in the oral mucosa. |
format | Online Article Text |
id | pubmed-10272380 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-102723802023-06-17 Human polyomavirus BKPyV and JCPyV serostatus has no impact on women´s human papillomavirus infection outcome Laine, Hanna K. Waterboer, Tim Syrjänen, Kari Grenman, Seija Louvanto, Karolina Syrjänen, Stina Front Cell Infect Microbiol Cellular and Infection Microbiology INTRODUCTION: Polyomaviruses have both structural and functional similarities with papillomaviruses. Accordingly, their role in human papillomavirus (HPV) associated malignancies has been studied with conflicting results. Our goal was to disclose any association between BK (BKPyV) and/or JC (JCPyV) polyomavirus serology and HPV data derived from Finnish women (327) in a 6-year prospective follow-up. METHODS: Glutathione S-transferase fusion-protein-capture (ELISA) in combination with fluorescent bead technology was used to analyze antibodies to BKPyV and JCPyV. In the longitudinal setting, BKPyV or JCPyV serostatus was related to i) oral- and ii) genital low (LR)- and high risk (HR) HPV DNA detection, iii) HPV16 persistence at both these sites, iv) results of the Pap (Papanicolaou) smear taken at baseline, and v) development of incident CIN (cervical intraepithelial neoplasia) during the follow-up. RESULTS: Being BKPyV or JCPyV seropositive was not significantly associated with HPV seropositivity to either LR- or HR-genotypes, genital- or oral HPV DNA positivity, persistence of genital- or oral HPV16 infection, grade of Pap smear, or development of incident CIN. DISCUSSION: Thus, the present study could not provide any confirmation to the concept that co-infections by HPyV and HPV have interactions that impact on the clinical manifestations or outcomes of HPV infections either in the genital tract or in the oral mucosa. Frontiers Media S.A. 2023-06-02 /pmc/articles/PMC10272380/ /pubmed/37333846 http://dx.doi.org/10.3389/fcimb.2023.1190019 Text en Copyright © 2023 Laine, Waterboer, Syrjänen, Grenman, Louvanto and Syrjänen https://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 | Cellular and Infection Microbiology Laine, Hanna K. Waterboer, Tim Syrjänen, Kari Grenman, Seija Louvanto, Karolina Syrjänen, Stina Human polyomavirus BKPyV and JCPyV serostatus has no impact on women´s human papillomavirus infection outcome |
title | Human polyomavirus BKPyV and JCPyV serostatus has no impact on women´s human papillomavirus infection outcome |
title_full | Human polyomavirus BKPyV and JCPyV serostatus has no impact on women´s human papillomavirus infection outcome |
title_fullStr | Human polyomavirus BKPyV and JCPyV serostatus has no impact on women´s human papillomavirus infection outcome |
title_full_unstemmed | Human polyomavirus BKPyV and JCPyV serostatus has no impact on women´s human papillomavirus infection outcome |
title_short | Human polyomavirus BKPyV and JCPyV serostatus has no impact on women´s human papillomavirus infection outcome |
title_sort | human polyomavirus bkpyv and jcpyv serostatus has no impact on women´s human papillomavirus infection outcome |
topic | Cellular and Infection Microbiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10272380/ https://www.ncbi.nlm.nih.gov/pubmed/37333846 http://dx.doi.org/10.3389/fcimb.2023.1190019 |
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