Abstract

BackgroundFew studies focused on longitudinal modifications over time of high-risk HPV (HR-HPV) at anal and oral sites in HIV+ men who have sex with men (MSM).MethodsWe described patterns and longitudinal changes of HR-HPV detection and the prevalence of HR-HPV covered by the nonavalent HPV vaccine (vax-HPV) at oral and anal sites in 165 HIV+ MSM followed in an Italian hospital. The samples were collected at baseline and after 24 months (follow-up). The presence of HPV was investigated with Inno-LiPA HPV Genotyping Extra II.ResultsMedian age was 44 years (IQR 36–53), median CD4+ cell count at nadir was 312 cells/mm3 (IQR 187–450). A total of 120 subjects (72.7%) were receiving successful antiretroviral therapy (ART). At baseline and follow-up, the frequency of HR-HPV was significantly higher in the anal site (65.4% vs 9.4 and 62.4% vs 6.8%, respectively). Only 2.9% of subjects were persistently HR-HPV negative at both sites. All oral HR-HPV were single at baseline vs 54.6% at baseline at the anal site (p = 0.005), and all oral HR-HPV were single at follow-up vs 54.4% at anal site at follow-up (p = 0.002). The lowest rate of concordance between the oral and anal results was found for HR-HPV detection; almost all HR-HPV positive results at both anal and oral sites had different HR-HPV.The most frequent HR-HPV in anal swabs at baseline and follow-up were HPV-16 and HPV-52.At follow-up at anal site, 37.5% of patients had different HR-HPV genotypes respect to baseline, 28.8% of subjects with 1 HR-HPV at baseline had an increased number of HR-HPV, and patients on ART showed a lower frequency of confirmed anal HR-HPV detection than untreated patients (p = 0.03) over time. Additionally,54.6 and 50.5% of patients had only HR-vax-HPV at anal site at baseline and follow-up, respectively; 15.2% had only HR-vax-HPV at baseline and follow-up.ConclusionsWe believe that it is important testing multiple sites over time in HIV-positive MSM. ART seems to protect men from anal HR-HPV confirmed detection. Vaccination programmes could reduce the number of HR-HPV genotypes at anal site and the risk of the first HR-HPV acquisition at the oral site.

Highlights

  • Few studies focused on longitudinal modifications over time of high-risk human papillomavirus (HPV) (HR-HPV) at anal and oral sites in HIV+ men who have sex with men (MSM)

  • The aim of this work was to analyze the numerosity and the confirmed detection of oral and anal HPV infection over a 24-month period in a cohort of HIV-positive MSM; we focused on pattern and longitudinal changes in high-risk HPV (HR-HPV) detection and the prevalence of HPV genotypes covered by the nonavalent HPV vaccine

  • This study focused on the characteristics of persistence and pattern evolution of HR-HPV infection in oral and anal areas over time in a cohort of HIV-positive MSM

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Summary

Introduction

Few studies focused on longitudinal modifications over time of high-risk HPV (HR-HPV) at anal and oral sites in HIV+ men who have sex with men (MSM). Within the HIV positive population, over 80% of men who have sex with men (MSM) were HPV-positive in the anal canal, being higher than 80% and with a high frequency (ranging from 70 to 90%) of high risk HPV (HR-HPV) in most studies [1, 2]. Marra et al [5] reported that only anal HPV DNA persistence was independently associated with anal high-grade squamous intraepithelial lesions both in general and by concordant causative HPV-type in a cohort of HIV-positive MSM with a mean nadir CD4 T-cell count of 245 ± 134 cells/mm. Limited evidence-based data on the independent role of longterm HPV DNA positivity on the incidence of head and neck squamous cell carcinoma in HIV+ MSM are available [6]

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