Possible Reactivation of Latent Anal Human Papillomavirus Associated with Markers of Immune Dysfunction in Gay and Bisexual Men

Author:

Poynten I. Mary1ORCID,Jin Fengyi1,Molano Monica23,Roberts Jennifer M.4ORCID,Hillman Richard J.25ORCID,Templeton David J.267ORCID,Law Carmella25,Stanley Margaret A.8,Waterboer Tim9,Farnsworth Annabelle4ORCID,Fairley Christopher K.10,Garland Suzanne M.2311,Grulich Andrew E.1

Affiliation:

1. 1The Kirby Institute, Wallace Wurth Building, University of New South Wales, Kensington, Sydney, New South Wales, Australia.

2. 2Centre for Women's Infectious Diseases, The Royal Women's Hospital, Parkville, Melbourne, Victoria, Australia.

3. 3Molecular Microbiology, Murdoch Children's Research Institute, Parkville, Melbourne, Victoria, Australia.

4. 4Douglass Hanly Moir Pathology, Macquarie Park, Sydney, New South, Wales, Australia.

5. 5St Vincent's Hospital, Darlinghurst, Sydney, New South Wales, Australia.

6. 6Department of Sexual Health Medicine, Sydney Local Health District, Camperdown, Sydney, New South Wales, Australia.

7. 7Sydney Medical School, University of Sydney, Sydney, New South Wales, Australia.

8. 8German Cancer Research Center (DKFZ), Heidelberg, Germany.

9. 9Department of Pathology, University of Cambridge, Cambridge, United Kingdom.

10. 10Central Clinical School, Monash University, Melbourne, Victoria, Australia.

11. 11Department of Obstetrics and Gynaecology, University of Melbourne, Parkville, Melbourne, Victoria, Australia.

Abstract

Abstract Background: It is unknown whether reactivation of human papillomavirus (HPV) after latency occurs in the anus. We measured incidence and predictors of incident anal HPV in sexually inactive gay and bisexual men (GBM) as a surrogate of HPV reactivation. Methods: The Study of the Prevention of Anal Cancer collected data on sexual behavior, anal cytology, HPV DNA, histology and HPV serology. HPV incidence during periods when zero sexual partners were reported in the last six months at both the current and previous annual visit (“no sexual activity”) was analyzed by Cox regression using the Wei-Lin-Weissfeld method to determine univariable predictors. Results: Of 617 men enrolled, 525 had results for ≥2 visits, of whom 58 (11%) had ≥ one period of “no sexual activity”. During sexually inactive periods, there were 29 incident high risk HPV infections in 20 men, which occurred more commonly in older men (Ptrend = 0.010), HIV-positive men (HR = 3.12; 95% CI, 0.91–16.65), longer duration of HIV (Ptrend = 0.028), history of AIDS defining illness (P = 0.010), lower current (P = 0.010) and nadir CD4 count (P = 0.014). For 18 of 29 infections with available results, 12 men remained type-specific HRHPV L1 seronegative. None were consistently seropositive. A new diagnosis of HSIL occurred in only two men, caused by an HPV type other than the incident type. Conclusions: Our findings suggest that in sexually inactive GBM, anal HRHPV incidence is relatively common, and is associated with increasing age and immune dysfunction, a pattern consistent with HPV reactivation. Impact: Reactivation of anal HPV may occur.

Funder

National Health and Medical Research Council Program Grant

Cancer Council New South Wales Strategic Research Partnership Program Grant

Publisher

American Association for Cancer Research (AACR)

Subject

Oncology,Epidemiology

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