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  4. Dynamics of anal HPV infection after 9vHPV vaccination in men who have sex with men (MSM) with HIV: A prospective, controlled cohort study.
 
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Dynamics of anal HPV infection after 9vHPV vaccination in men who have sex with men (MSM) with HIV: A prospective, controlled cohort study.

Journal
Human vaccines & immunotherapeutics
Journal Volume
22
Journal Issue
1
Start Page
Article number 2618876
ISSN
2164-554X
Date Issued
2026-12
Author(s)
KUAN-YIN LIN  
Lai, Shuo-Lun
YU-SHAN HUANG  
HSIN-YUN SUN  
YU-CHUNG CHUANG  
Liu, Wen-Chun
I-SHIOW JAN  
CHIEN-CHING HUNG  
CHI-TAI FANG  
DOI
10.1080/21645515.2026.2618876
URI
https://scholars.lib.ntu.edu.tw/handle/123456789/736009
Abstract
Men who have sex with men (MSM) with HIV are disproportionately affected by persistent human papillomavirus (HPV) infections and related anogenital cancers. No controlled trial has evaluated the efficacy of the nonavalent HPV vaccine (9vHPV) in this population. This prospective, controlled cohort study offered eligible MSM with HIV a 3-dose 9vHPV series and followed both the vaccinated group (vaccinees) and the unvaccinated group (controls). Anal specimens were collected for HPV genotyping, cytology, and microbiota profiling. The primary outcomes were the clearance and incidence of 9vHPV-covered HPV types. Baseline vaccine-type HPV prevalence was 41.0% in vaccinees (n = 39; median age, 33 y; median CD4, 682/μl) and 39.3% in controls (n = 56; median age, 35 y; median CD4, 679/μl) ( = .865). At month 3, 75.0% of vaccinees with prevalent HPV infection had cleared at least one genotype, and 85.7% of those with abnormal baseline cytology experienced regression. However, clearance rates (per 1000 person-months) were 46.3 (vaccine type) and 56.0 (non-vaccine type) in vaccinees versus 64.1 and 91.8 in controls ( = .456 and 0.371). HPV incidence was 19.5 (vaccine type) and 15.1 (non-vaccine type) in vaccinees versus 12.4 and 12.4 in controls ( = .378 and 0.710). 9vHPV vaccination was not associated with enhanced clearance (aHR, 0.27; 95% CI, 0.11-0.68) or decreased incidence of vaccine-type HPV (aHR, 0.44; 95% CI, 0.11-1.82). No significant differences were observed in anal dysplasia regression or anal microbiota composition over 12 months. Given the lack of short-term secondary benefit and persistence of HPV incidence, MSM with HIV require continued routine anal cancer screening.
Subjects
Clearance
anal cancer screening
anal cytology
microbiota
precancerous lesion
regression
sexually transmitted infection
Type
journal article

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