The effects of bivalent human papillomavirus (HPV) vaccination on high-risk anogenital HPV infection among sexually active female adolescents with and without perinatally acquired HIV.
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Ounchanum Pradthana, Ounchanum Pradthana, Achalapong Jullapong, Achalapong Jullapong, Teeraananchai Sirinya, Teeraananchai Sirinya, Gatechompol Sivaporn, Gatechompol Sivaporn, Phongsamart Wanatpreeya, Phongsamart Wanatpreeya, Chokephaibulkit Kulkanya, Chokephaibulkit Kulkanya, Tran Dan Ngoc Hanh, Tran Dan Ngoc Hanh, Dang Hanh Le Dung, Dang Hanh Le Dung, Teeratakulpisarn Nipat, Teeratakulpisarn Nipat, Chalermchockcharoenkit Amphan, Chalermchockcharoenkit Amphan, Singtoroj Thida, Singtoroj Thida, Sohn Annette H, Sohn Annette H, Phanuphak Nittaya, Phanuphak Nittaya
Аннотация
METHODS: During a 3-year study, prevalent, incident, and persistent HR-HPV infection were assessed at annual visits. A subset of participants received a bivalent HPV vaccine. Samples were taken for HPV testing from the vagina, cervix, and anus. HR-HPV persistence was defined as the detection of the same genotype(s) at any anogenital compartment over≥two consecutive visits.
RESULTS: Of the 93 PHIV and 99 HIV-negative female youth enrolled in this study, 25 (27%) PHIV and 22 (22%) HIV-negative youth received a HPV vaccine. Persistent infection with any HR-HPV type was significantly lower among PHIV youth who received the vaccine compared to those who did not (33%vs 61%, P =0.02); a difference was not observed among HIV-negative youth (35%vs 50%, P =0.82). PHIV infection (adjusted prevalence ratio [aPR] 2.31, 95% CI 1.45-3.67) and not receiving a HPV vaccine (aPR, 1.19, 95%CI 1.06-1.33) were associated with persistent anogenital HR-HPV infection.
CONCLUSIONS: Bivalent HPV vaccination after initiation of sexual activity was associated with reduced persistence of anogenital HR-HPV infection in Southeast Asian PHIV female youth, which may be related to vaccine cross-protection. Primary and catch-up HPV vaccinations should be prioritised for children and youth with HIV.