The Journal of Infectious Diseases · 2002 · 48 citations · 16 references
Life SciencesInfectious DiseasesMolecular GeneticsMolecular VirologyPharmacogeneticsVirologyAntiretroviral TherapyAntiviral Drug ResistanceMutation AnalysisVariant AnalysisViral EvolutionViral MutationClonal Evolution AnalysisClonal Mutation AnalysisGenotyping For ResistanceProtease Inhibitor ResistanceReal-time Polymerase Chain Reaction (Pcr)Real-time Polymerase Chain Reaction AssaysResistance Mutation DetectionResistance-associated Viral Variants
Conventional genotyping of human immunodeficiency virus type 1 often reveals a shift from a drug-resistant genotype to a wild-type genotype after treatment interruption. A real-time polymerase chain reaction-based technique was used to detect minority resistant populations in 13 patients who showed genotype reversion after interruption of treatment for 3 months. Sixty-two percent of patients in whom the V82A and L90M protease mutations were no longer detectable by conventional genotyping still harbored minority resistant variants, in proportions ranging from 0.1% to 21%. None of the patients with these minority resistant variants who received a protease-inhibitor regimen on resumption of therapy had a response to treatment. However, population sequencing and clonal analysis of plasma samples obtained 1-2 months after resumption of treatment revealed the presence of wild-type virus during the initial decline in plasma virus load, which indicates that minority resistant variants were not rapidly selected.
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Steven G. Deeks, Terri Wrin, Teri Liegler et al. · New England Journal of Medicine · 2001 · 661 citations · Full text
Martin S. Hirsch, Huldrych F. Günthard, Jonathan Schapiro et al. · Clinical Infectious Diseases · 2008 · 573 citations · Full text
Rapid decline in detectability of HIV-1 drug resistance mutations after stopping therapy
Helen Devereux, Mike Youle, Margaret Johnson et al. · AIDS · 1999 · 287 citations