Linked dual-class HIV resistance mutations are associated with treatment failure.
Anti-HIV Agents
/ administration & dosage
Antineoplastic Combined Chemotherapy Protocols
/ administration & dosage
Drug Resistance, Viral
/ drug effects
Emtricitabine
/ administration & dosage
Female
Genome, Viral
HIV Infections
/ drug therapy
HIV-1
/ drug effects
Humans
Mutation
Nevirapine
/ administration & dosage
Tenofovir
/ administration & dosage
Treatment Failure
Whole Genome Sequencing
AIDS/HIV
Drug therapy
Journal
JCI insight
ISSN: 2379-3708
Titre abrégé: JCI Insight
Pays: United States
ID NLM: 101676073
Informations de publication
Date de publication:
03 10 2019
03 10 2019
Historique:
received:
07
05
2019
accepted:
27
08
2019
pubmed:
6
9
2019
medline:
21
10
2020
entrez:
6
9
2019
Statut:
epublish
Résumé
We hypothesized that HIV-1 with dual-class but not single-class drug resistance mutations linked on the same viral genome, present in the virus population before initiation of antiretroviral therapy (ART), would be associated with failure of ART to suppress viremia. To test this hypothesis, we utilized an ultrasensitive single-genome sequencing assay that detects rare HIV-1 variants with linked drug resistance mutations (DRMs). A case (ART failure) control (nonfailure) study was designed to assess whether linkage of DRMs in pre-ART plasma samples was associated with treatment outcome in the nevirapine/tenofovir/emtricitabine arm of the AIDS Clinical Trials Group A5208/Optimal Combined Therapy After Nevirapine Exposure (OCTANE) Trial 1 among women who had received prior single-dose nevirapine. Ultrasensitive single-genome sequencing revealed a significant association between pre-ART HIV variants with DRMs to 2 drug classes linked on the same genome (dual class) and failure of combination ART with 3 drugs to suppress viremia. In contrast, linked, single-class DRMs were not associated with ART failure. We conclude that linked dual-class DRMs present before the initiation of ART are associated with ART failure, whereas linked single-class DRMs are not.
Identifiants
pubmed: 31487271
pii: 130118
doi: 10.1172/jci.insight.130118
pmc: PMC6795402
doi:
pii:
Substances chimiques
Anti-HIV Agents
0
Nevirapine
99DK7FVK1H
Tenofovir
99YXE507IL
Emtricitabine
G70B4ETF4S
Banques de données
ClinicalTrials.gov
['NCT00089505']
Types de publication
Clinical Trial, Phase I
Journal Article
Randomized Controlled Trial
Research Support, N.I.H., Extramural
Research Support, N.I.H., Intramural
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Subventions
Organisme : NIAID NIH HHS
ID : UM1 AI069494
Pays : United States
Organisme : NIAID NIH HHS
ID : UM1 AI069501
Pays : United States
Organisme : NIAID NIH HHS
ID : UM1 AI069456
Pays : United States
Organisme : NIAID NIH HHS
ID : U01 AI069453
Pays : United States
Organisme : NIAID NIH HHS
ID : U01 AI069463
Pays : United States
Organisme : NIAID NIH HHS
ID : U01 AI032775
Pays : United States
Organisme : NIAID NIH HHS
ID : UM1 AI069453
Pays : United States
Organisme : NIAID NIH HHS
ID : U01 AI069518
Pays : United States
Organisme : NIAID NIH HHS
ID : U01 AI069426
Pays : United States
Organisme : NIAID NIH HHS
ID : UM1 AI106701
Pays : United States
Organisme : NIAID NIH HHS
ID : U01 AI069456
Pays : United States
Organisme : NIAID NIH HHS
ID : U01 AI069436
Pays : United States
Organisme : NIAID NIH HHS
ID : UM1 AI068636
Pays : United States
Organisme : NIAID NIH HHS
ID : UM1 AI069426
Pays : United States
Organisme : NCI NIH HHS
ID : R35 CA200421
Pays : United States
Organisme : NIAID NIH HHS
ID : UM1 AI068634
Pays : United States
Organisme : NIAID NIH HHS
ID : U01 AI069501
Pays : United States
Organisme : NIAID NIH HHS
ID : U01 AI069455
Pays : United States
Organisme : NIAID NIH HHS
ID : UM1 AI108568
Pays : United States
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