Human papillomavirus 68 subtypes among people with human immunodeficiency virus and implications for anal screening
6 affiliations
- 1Infectious Diseases Unit, Hospital General Universitario de Elche, Elche, Spain
- 2CIBER de Enfermedades Infecciosas, Instituto de Salud Carlos III, Madrid, Spain
- 3FISABIO, Valencia, Spain
- 4Hospital Universitario Infanta Leonor, Madrid, Spain
- 5Universidad Miguel Hernández de Elche, Elche, Spain
- 6Microbiology Service, Hospital General Universitario de Elche, Elche, Spain
Abstract
Background: Human papillomavirus (HPV) infection is a key risk factor for anal cancer. While HPV16’s carcinogenic role is well established, the contribution of other high-prevalence genotypes in people with HIV (PWH), such as HPV68 is less defined. This study examines the prevalence of HPV68 subtypes, their oncogene expression, and association with histologically confirmed high-grade squamous intraepithelial lesions (HSIL).
Methods: Two hundred PWH with abnormal anal cytology underwent HPV genotyping and mRNA analysis for the E6/E7 oncogenes of HPV16 and HPV68. Statistical analyses evaluated associations between HPV genotypes, oncogene expression, and HSIL.
Results: The cohort had a median age of 50 (IQR, 43-57) years, with 83% male participants and 93.9% virologically suppressed. HSIL was confirmed by histology in 25% of participants. HPV68 (28.5%) and HPV16 (24.5%) were the most prevalent genotypes, with HPV68a detected in 65.3% of HPV68-positive cases. Among HSIL cases, HPV16 (42%) and HPV68 (34%) were most common. HPV68a was significantly associated with HSIL in participants without HPV16. mRNA expression levels of E6 and E7 from HPV68a were significantly higher in the HSIL group (142.0 vs 12.9, p = 0.007 and 82.5 vs 9.1, p = 0.014, respectively). Differences remained significant after adjusting for the number of HPV genotypes and HPV16.
Conclusions: These findings suggest that HPV68a drives anal HSIL and warrants inclusion in screening and vaccination for high-risk groups.
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BibTeX
@article{belloperez2026human,
title = {{Human papillomavirus 68 subtypes among people with human immunodeficiency virus and implications for anal screening}},
author = {M. Bello-Perez and A. Gutiérrez-Ortiz de la Tabla and P. Mascarell and JA García and A. Galiana and M. Fernández-González and J. García-Abellán and S. Padilla and F. Gutiérrez and M. Masiá},
journal = {Communications Medicine},
year = {2026},
month = jul,
doi = {10.1038/s43856-026-01717-0},
url = {https://doi.org/10.1038/s43856-026-01717-0},
note = {CC BY-NC-ND 4.0},
}
RIS
TY - JOUR
TI - Human papillomavirus 68 subtypes among people with human immunodeficiency virus and implications for anal screening
AU - M. Bello-Perez
AU - A. Gutiérrez-Ortiz de la Tabla
AU - P. Mascarell
AU - JA García
AU - A. Galiana
AU - M. Fernández-González
AU - J. García-Abellán
AU - S. Padilla
AU - F. Gutiérrez
AU - M. Masiá
PY - 2026
DA - 2026/07/03
JO - Communications Medicine
DO - 10.1038/s43856-026-01717-0
UR - https://doi.org/10.1038/s43856-026-01717-0
AB - Background: Human papillomavirus (HPV) infection is a key risk factor for anal cancer. While HPV16’s carcinogenic role is well established, the contribution of other high-prevalence genotypes in people with HIV (PWH), such as HPV68 is less defined. This study examines the prevalence of HPV68 subtypes, their oncogene expression, and association with histologically confirmed high-grade squamous intraepithelial lesions (HSIL). Methods: Two hundred PWH with abnormal anal cytology underwent HPV genotyping and mRNA analysis for the E6/E7 oncogenes of HPV16 and HPV68. Statistical analyses evaluated associations between HPV genotypes, oncogene expression, and HSIL. Results: The cohort had a median age of 50 (IQR, 43-57) years, with 83% male participants and 93.9% virologically suppressed. HSIL was confirmed by histology in 25% of participants. HPV68 (28.5%) and HPV16 (24.5%) were the most prevalent genotypes, with HPV68a detected in 65.3% of HPV68-positive cases. Among HSIL cases, HPV16 (42%) and HPV68 (34%) were most common. HPV68a was significantly associated with HSIL in participants without HPV16. mRNA expression levels of E6 and E7 from HPV68a were significantly higher in the HSIL group (142.0 vs 12.9, p = 0.007 and 82.5 vs 9.1, p = 0.014, respectively). Differences remained significant after adjusting for the number of HPV genotypes and HPV16. Conclusions: These findings suggest that HPV68a drives anal HSIL and warrants inclusion in screening and vaccination for high-risk groups.
SN - 2730-664X
ER -