Dolutegravir Resistance in African Programmatic Settings Among Patients With Failure of Dolutegravir-based ART.

HIV-1 antiretroviral drug resistance dolutegravir sub-Saharan Africa virologic failure

Journal

Open forum infectious diseases
ISSN: 2328-8957
Titre abrégé: Open Forum Infect Dis
Pays: United States
ID NLM: 101637045

Informations de publication

Date de publication:
Jul 2024
Historique:
received: 24 05 2024
accepted: 04 06 2024
medline: 1 7 2024
pubmed: 1 7 2024
entrez: 1 7 2024
Statut: epublish

Résumé

Dolutegravir resistance is emerging in routine clinical contexts in southern Africa, primarily in patients with prior treatment experience failing dolutegravir-based antiretroviral therapy (ART). This potential issue was raised by The Nucleosides and Darunavir/Dolutegravir in Africa trial that compared dolutegravir and boosted protease inhibitor-based therapy as second-line ART, in which new dolutegravir resistance was observed at failure. However, recent data suggest that also at risk are patients who were transitioned to dolutegravir from non-nucleoside reverse transcriptase inhibitor-based ART while viremic. Identifying patients experiencing failure of dolutegravir with resistance will be difficult given current gaps in viral load monitoring and limited capacity for genotypic resistance testing. As a result, in the short term, most patients affected will go unrecognized, with particularly important implications for patients affected who have advanced HIV or who are pregnant/breastfeeding. Prospective research is needed to understand the scope of the problem, identify additional risk factors, and determine best management. In the short term, for most patients with dolutegravir resistance and prior non-nucleoside reverse transcriptase inhibitor exposure, the best option will be a timely switch to a regimen anchored by a boosted protease inhibitor, with a high genetic barrier to resistance.

Identifiants

pubmed: 38947737
doi: 10.1093/ofid/ofae321
pii: ofae321
pmc: PMC11214099
doi:

Types de publication

Journal Article

Langues

eng

Pagination

ofae321

Informations de copyright

© The Author(s) 2024. Published by Oxford University Press on behalf of Infectious Diseases Society of America.

Déclaration de conflit d'intérêts

Potential conflicts of interest. All authors: No reported conflicts of interest and no reported disclosures.

Auteurs

Richard A Murphy (RA)

Division of Infectious Diseases, Geisel School of Medicine at Dartmouth, Hanover, New Hampshire, USA.
Division of Infectious Diseases, White River Junction Veterans Affairs Medical Center, White River Junction, Vermont, USA.

Pradeep H Bedesi (PH)

HAST Unit, RK Khan Hospital, Durban, South Africa.

Nirmala Perumal (N)

HAST Unit, RK Khan Hospital, Durban, South Africa.

Bernadett I Gosnell (BI)

Department of Infectious Diseases, University of KwaZulu-Natal, Durban, South Africa.

Timothy J Hatlen (TJ)

Division of HIV, Lundquist Institute for Biomedical Innovation at Harbor-University of California Los Angeles Medical Center, Torrance, California, USA.

Jaysingh Brijkumar (J)

HAST Unit, RK Khan Hospital, Durban, South Africa.

Classifications MeSH