A1 Refereed original research article in a scientific journal

Human polyomavirus BKPyV and JCPyV serostatus has no impact on women´s human papillomavirus infection outcome




AuthorsLaine Hanna K., Waterboer Tim, Syrjänen Kari, Grenman Seija, Louvanto Karolina, Syrjänen Stina

PublisherFRONTIERS MEDIA SA

Publication year2023

JournalFrontiers in Cellular and Infection Microbiology

Journal name in sourceFRONTIERS IN CELLULAR AND INFECTION MICROBIOLOGY

Journal acronymFRONT CELL INFECT MI

Article number 1190019

Volume13

Number of pages8

ISSN2235-2988

eISSN2235-2988

DOIhttps://doi.org/10.3389/fcimb.2023.1190019

Web address https://doi.org/10.3389/fcimb.2023.1190019

Self-archived copy’s web addresshttps://research.utu.fi/converis/portal/detail/Publication/180000452


Abstract

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.


Downloadable publication

This is an electronic reprint of the original article.
This reprint may differ from the original in pagination and typographic detail. Please cite the original version.





Last updated on 2024-26-11 at 14:13