Anal dysplasia and HIV shedding in ART-treated men.


Journal

Sexually transmitted infections
ISSN: 1472-3263
Titre abrégé: Sex Transm Infect
Pays: England
ID NLM: 9805554

Informations de publication

Date de publication:
09 2020
Historique:
received: 06 09 2019
revised: 05 12 2019
accepted: 12 12 2019
pubmed: 8 1 2020
medline: 12 9 2020
entrez: 8 1 2020
Statut: ppublish

Résumé

Anal human papillomavirus (HPV) infection is highly prevalent among men who have sex with men (MSM). HPV-associated anal dysplasia has been linked with anal HIV RNA shedding despite antiretroviral therapy (ART). Since mucosal HIV levels are a key determinant of sexual transmission of the virus, this would have important public health implications. Therefore, we assessed the association between anal dysplasia and HIV shedding in ART-treated MSM from Toronto, Canada. In 54 HIV-infected men on effective ART, we assessed anal HIV RNA shedding by PCR, HPV infection by microsphere-based genotyping and anal dysplasia by high-resolution anoscopy. All participants were enrolled between May 2017 and October 2018. The median duration of ART at the time of study enrolment was 18 years, with most participants being on an integrase inhibitor-based ART regimen. Low-level anal HIV RNA shedding was present in 15/54 (27.8%) participants. Neither the detection of shedding nor the level of HIV RNA was associated with anal dysplasia, HPV infection or antiretroviral regimen. HPV-associated anal dysplasia was not associated with anal HIV RNA shedding in this relatively small cohort of men on effective ART. While anal HIV RNA was detected more often than anticipated, shedding was low level and unlikely to cause HIV transmission. However, the immunological drivers of anal HIV RNA shedding in ART-treated individuals may merit further study.

Identifiants

pubmed: 31907327
pii: sextrans-2019-054262
doi: 10.1136/sextrans-2019-054262
doi:

Substances chimiques

Anti-HIV Agents 0
HIV Integrase Inhibitors 0
RNA, Viral 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

399-401

Subventions

Organisme : CIHR
ID : TE2-138200
Pays : Canada

Informations de copyright

© Author(s) (or their employer(s)) 2020. No commercial re-use. See rights and permissions. Published by BMJ.

Déclaration de conflit d'intérêts

Competing interests: YC is supported by the Canadian Institutes of Health Research (CIHR) studentship, and RK is supported by the Ontario HIV Treatment Network (OHTN) Endowed Chair in HIV Research at the University of Toronto.

Auteurs

Yoojin Choi (Y)

Department of Immunology, University of Toronto, Toronto, Ontario, Canada yoojin.choi21@gmail.com.

Irving Salit (I)

Department of Medicine, University Health Network, Toronto, Ontario, Canada.

Sarah Grech (S)

Department of Immunology, University of Toronto, Toronto, Ontario, Canada.

Marie Sano (M)

Department of Medicine, University Health Network, Toronto, Ontario, Canada.

Edward Weiss (E)

Department of Medicine, University Health Network, Toronto, Ontario, Canada.

Colin Kovacs (C)

Maple Leaf Medical Clinic, Toronto, Ontario, Canada.

Rachelle Paquette (R)

Department of Medicine, University Health Network, Toronto, Ontario, Canada.

Marian Claudio (M)

Department of Medicine, University Health Network, Toronto, Ontario, Canada.

Suzanne Gibbons (S)

National Microbiology Laboratory, Public Health Agency of Canada, Winnipeg, Winnipeg, Manitoba, Canada.

Alberto Severini (A)

National Microbiology Laboratory, Public Health Agency of Canada, Winnipeg, Winnipeg, Manitoba, Canada.
Department of Medical Microbiology and Infectious Diseases, University of Manitoba, Winnipeg, Manitoba, Canada.

Rupert Kaul (R)

Department of Immunology, University of Toronto, Toronto, Ontario, Canada.
Department of Medicine, University Health Network, Toronto, Ontario, Canada.

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