Frequency of Hepatitis B Virus Resistance Mutations in Women Using Tenofovir Gel as Pre-Exposure Prophylaxis.


Journal

Viruses
ISSN: 1999-4915
Titre abrégé: Viruses
Pays: Switzerland
ID NLM: 101509722

Informations de publication

Date de publication:
19 06 2019
Historique:
received: 14 05 2019
revised: 12 06 2019
accepted: 14 06 2019
entrez: 29 6 2019
pubmed: 30 6 2019
medline: 25 7 2020
Statut: epublish

Résumé

Intermittent use of a single antiretroviral agent in the presence of a replicating virus could potentially increase the development of antiviral resistance. The pericoital, before-and-after sex, dosing regimen used in the Centre for the AIDS Programme of Research in South Africa (CAPRISA) 004 tenofovir gel trial meant that women who were infected with hepatitis B virus (HBV) were exposed intermittently to tenofovir during their participation. The impact of this dosing regimen on HBV resistance was assessed by amplification of the HBV polymerase region from 37 stored plasma samples of women who were HBV surface antigen positive. All samples belonged to HBV genotype A. None of the known tenofovir resistance mutations (M240V/I, L180M, A194T, V214A, N238T) were identified in any individuals. While it is reassuring that no resistance mutations were found among women using topical tenofovir, the rapidly expanding access to oral tenofovir-containing HIV pre-exposure prophylaxis (PrEP), with higher systemic exposure to the drug, makes monitoring for potential HBV drug resistance important.

Identifiants

pubmed: 31248149
pii: v11060569
doi: 10.3390/v11060569
pmc: PMC6630952
pii:
doi:

Substances chimiques

Antiviral Agents 0
DNA, Viral 0
Tenofovir 99YXE507IL

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, Non-P.H.S.

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : NIDDK NIH HHS
ID : P30 DK078392
Pays : United States
Organisme : FIC NIH HHS
ID : D43TW00231
Pays : United States
Organisme : NIH HHS
ID : 5R24TW008863
Pays : United States

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Auteurs

Cheryl Baxter (C)

Centre for the AIDS Programme of Research in South Africa (CAPRISA), University of KwaZulu-Natal, Private Bag X7, Congella, 4013, Durban, South Africa. Cheryl.baxter@caprisa.org.

Sinaye Ngcapu (S)

Centre for the AIDS Programme of Research in South Africa (CAPRISA), University of KwaZulu-Natal, Private Bag X7, Congella, 4013, Durban, South Africa. sinaye.ngcapu@caprisa.org.

Jason T Blackard (JT)

Division of Digestive Diseases, Department of Internal Medicine, College of Medicine, University of Cincinnati, Cincinnati, OH 45267, USA. blackajt@ucmail.uc.edu.

Eleanor A Powell (EA)

Division of Digestive Diseases, Department of Internal Medicine, College of Medicine, University of Cincinnati, Cincinnati, OH 45267, USA. powelleo@ucmail.uc.edu.

Patricia K Penton (PK)

Division of Digestive Diseases, Department of Internal Medicine, College of Medicine, University of Cincinnati, Cincinnati, OH 45267, USA. pkpenton@gmail.com.

Salim S Abdool Karim (SS)

Centre for the AIDS Programme of Research in South Africa (CAPRISA), University of KwaZulu-Natal, Private Bag X7, Congella, 4013, Durban, South Africa. salim.abdoolkarim@caprisa.org.
Department of Epidemiology, Mailman School of Public Health, Columbia University, New York, NY 10032, USA. salim.abdoolkarim@caprisa.org.

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Classifications MeSH