Publication | Open Access
Sensitive Drug‐Resistance Assays Reveal Long‐Term Persistence of HIV‐1 Variants with the K103N Nevirapine (NVP) Resistance Mutation in Some Women and Infants after the Administration of Single‐Dose NVP: HIVNET 012
188
Citations
8
References
2005
Year
ImmunodeficienciesImmunologyAntiviral DrugDrug ResistanceHiv/aids CounsellingHuman RetrovirusResistance Mutation (Virology)Resistance MutationHivnet 012K103n NevirapineVirologyChronic Viral InfectionHivPharmacologySensitive Resistance AssaysAids PathogenesisHiv-1 EvolutionAntiviral TherapyHiv‐1 VariantsMedicine
BackgroundThe HIV Network for Prevention Trials (HIVNET) 012 trial showed that NVP resistance (NVPR) emerged in some women and children after the administration of single-dose nevirapine (SD-NVP). We tested whether K103N-containing human immunodeficiency virus (HIV)–1 variants persisted in women and infants 1 year or more after the administration of SD-NVP MethodsWe analyzed samples from 9 women and 5 infants in HIVNET 012 who had NVPR 6–8 weeks after the administration of SD-NVP. Samples were analyzed with the ViroSeq system and with 2 sensitive resistance assays, LigAmp and TyHRT ResultsViroSeq detected the K103N mutation in 8 of 9 women and in 2 of 5 infants. LigAmp detected the K103N mutation at low levels in 8 of 9 women and in 4 of 5 infants. K103N was not detected by ViroSeq 12–24 months after the administration of SD-NVP but was detected by LigAmp in 3 of 9 women and in 1 of 5 infants. K103N was also detected in those samples by use of the TyHRT assay ConclusionsK103N-containing variants persist in some women and infants for 1 year or more after the administration of SD-NVP. Sensitive resistance assays may provide new insight into the impact of antiretroviral drug exposure on HIV-1 evolution
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