Effects of Urethritis on Human Immunodeficiency Virus (HIV) in Semen: Implications for HIV Prevention and Cure.


Journal

Clinical infectious diseases : an official publication of the Infectious Diseases Society of America
ISSN: 1537-6591
Titre abrégé: Clin Infect Dis
Pays: United States
ID NLM: 9203213

Informations de publication

Date de publication:
05 10 2021
Historique:
received: 27 05 2020
pubmed: 10 10 2020
medline: 21 10 2021
entrez: 9 10 2020
Statut: ppublish

Résumé

Prior to the widespread availability of antiretroviral therapy (ART), men living with human immunodeficiency virus (HIV) with urethritis had increased concentrations of HIV in semen. This study aims to better evaluate HIV shedding in men with urethritis receiving ART, and its implications for the cure of HIV. Men living with HIV with urethritis taking ART ≥12 weeks were enrolled at a sexually transmitted infections clinic in Lilongwe, Malawi. Study follow-up included visits at 1, 2, 4, 8, 12, 24, 36, and 48 weeks after urethritis diagnosis and treatment. Matched blood and semen samples were collected at all visits, and all additional episodes of urethritis were followed with extra visits 1, 2, and 4 weeks after treatment. There were 111 men enrolled in the study between January 2017-March 2019, and 77 (69%) were suppressed in the blood (<400 copies/mL). Among the 77 men, 87 episodes of urethritis were evaluated during follow-up. Of the 87 episodes, 15 episodes (17%) had instances of seminal viral shedding ≥400 copies/mL despite viral suppression in the blood. During nonurethritis follow-up, ≤6% of men at each visit had a viral load ≥400 copies/mL in the semen while maintaining viral suppression in the blood. An HIV cure requires the elimination of HIV from every body compartment, but available ART does not currently accomplish this. Our study highlights the male genital tract as a local source of HIV that can be reversibly activated. A better understanding of this phenomenon is important to advance the HIV cure field.

Sections du résumé

BACKGROUND
Prior to the widespread availability of antiretroviral therapy (ART), men living with human immunodeficiency virus (HIV) with urethritis had increased concentrations of HIV in semen. This study aims to better evaluate HIV shedding in men with urethritis receiving ART, and its implications for the cure of HIV.
METHODS
Men living with HIV with urethritis taking ART ≥12 weeks were enrolled at a sexually transmitted infections clinic in Lilongwe, Malawi. Study follow-up included visits at 1, 2, 4, 8, 12, 24, 36, and 48 weeks after urethritis diagnosis and treatment. Matched blood and semen samples were collected at all visits, and all additional episodes of urethritis were followed with extra visits 1, 2, and 4 weeks after treatment.
RESULTS
There were 111 men enrolled in the study between January 2017-March 2019, and 77 (69%) were suppressed in the blood (<400 copies/mL). Among the 77 men, 87 episodes of urethritis were evaluated during follow-up. Of the 87 episodes, 15 episodes (17%) had instances of seminal viral shedding ≥400 copies/mL despite viral suppression in the blood. During nonurethritis follow-up, ≤6% of men at each visit had a viral load ≥400 copies/mL in the semen while maintaining viral suppression in the blood.
CONCLUSIONS
An HIV cure requires the elimination of HIV from every body compartment, but available ART does not currently accomplish this. Our study highlights the male genital tract as a local source of HIV that can be reversibly activated. A better understanding of this phenomenon is important to advance the HIV cure field.

Identifiants

pubmed: 33033831
pii: 5919802
doi: 10.1093/cid/ciaa1529
pmc: PMC8492110
doi:

Substances chimiques

RNA, Viral 0

Types de publication

Journal Article Research Support, N.I.H., Extramural

Langues

eng

Sous-ensembles de citation

IM

Pagination

e2000-e2004

Subventions

Organisme : Malawi Ministry of Health
Organisme : Lilongwe District Health Office
Organisme : FIC NIH HHS
ID : D43 TW010060
Pays : United States
Organisme : NIH HHS
Pays : United States
Organisme : University of North Carolina
Organisme : NIAID NIH HHS
ID : R01 AI114320
Pays : United States
Organisme : NIDDK NIH HHS
ID : R01 DK108424
Pays : United States
Organisme : NIAID NIH HHS
ID : T32 AI070114
Pays : United States

Informations de copyright

© The Author(s) 2020. Published by Oxford University Press for the Infectious Diseases Society of America. All rights reserved. For permissions, e-mail: journals.permissions@oup.com.

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Auteurs

Jane S Chen (JS)

Department of Epidemiology, University of North Carolina, Chapel Hill, North Carolina, USA.

Mitch Matoga (M)

University of North Carolina Project, Malawi, Lilongwe, Malawi.

Cecilia Massa (C)

University of North Carolina Project, Malawi, Lilongwe, Malawi.

Gerald Tegha (G)

University of North Carolina Project, Malawi, Lilongwe, Malawi.

Beatrice Ndalama (B)

University of North Carolina Project, Malawi, Lilongwe, Malawi.

Naomi Bonongwe (N)

University of North Carolina Project, Malawi, Lilongwe, Malawi.

Esther Mathiya (E)

University of North Carolina Project, Malawi, Lilongwe, Malawi.

Edward Jere (E)

University of North Carolina Project, Malawi, Lilongwe, Malawi.

Gabriel Banda (G)

University of North Carolina Project, Malawi, Lilongwe, Malawi.

Amy J Loftis (AJ)

Institute for Global Health and Infectious Diseases, University of North Carolina, Chapel Hill, North Carolina, USA.

Kathryn E Lancaster (KE)

Division of Epidemiology, The Ohio State University College of Public Health, Columbus, Ohio, USA.

William C Miller (WC)

Department of Epidemiology, University of North Carolina, Chapel Hill, North Carolina, USA.
Division of Epidemiology, The Ohio State University College of Public Health, Columbus, Ohio, USA.

Irving F Hoffman (IF)

Institute for Global Health and Infectious Diseases, University of North Carolina, Chapel Hill, North Carolina, USA.

Myron S Cohen (MS)

Institute for Global Health and Infectious Diseases, University of North Carolina, Chapel Hill, North Carolina, USA.

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