Sub-Epidemics Explain Localized High Prevalence of Reduced Susceptibility to Rilpivirine in Treatment-Naive HIV-1-Infected Patients: Subtype and Geographic Compartmentalization of Baseline Resistance Mutations

Objective: The latest nonnucleoside reverse transcriptase inhibitor (NNRTI) rilpivirine (RPV) is indicated for human immunodeficiency virus type-1 (HIV-1) patients initiating antiretroviral treatment, but the extent of genotypic RPV resistance in treatment-naive patients outside clinical trials is poorly defined. Study Design: This retrospective observational study of clinical data from Belgium and Portugal evaluates genotypic information from HIV-1 drug-naive patients obtained for the purpose of drug resistance testing. Rilpivirine resistance-associated mutations (RPV-RAMs) were defined based... Mehr ...

Verfasser: Theys, Kristof
Van Laethem, Kristel
Gomes, Perpetua
Baele, Guy
Pineda-Peña, Andrea-Clemencia
Vandamme, Anne-Mieke
Camacho, Ricardo J.
Abecasis, Ana B.
Dokumenttyp: Artikel
Erscheinungsdatum: 2016
Verlag/Hrsg.: Mary Ann Liebert Inc.
Schlagwörter: Rilpivirine / Anti human immunodeficiency virus agent / Rna directed dna polymerase inhibitor / Antiviral resistance / Antiviral susceptibility / Article / Belgium / Epidemic / Founder effect / Genotype / Geographic distribution / Human / Human immunodeficiency virus 1 / Human immunodeficiency virus 1 infection / Human immunodeficiency virus infected patient / Major clinical study / Nonhuman / Observational study / Portugal / Prevalence / Priority journal / Resistance associated mutation / Retrospective study / Tablet / Virus mutation / Virus resistance / Drug effects / Genetics / Highly active antiretroviral therapy / Hiv infections / Mutation / Procedures / Single nucleotide polymorphism / Anti-hiv agents / Hiv-1 / Humans / Retrospective studies / Reverse transcriptase inhibitors / viral / single nucleotide / highly active / Antiretroviral therapy
Sprache: Englisch
Permalink: https://search.fid-benelux.de/Record/base-28929598
Datenquelle: BASE; Originalkatalog
Powered By: BASE
Link(s) : https://repository.urosario.edu.co/handle/10336/23941

Objective: The latest nonnucleoside reverse transcriptase inhibitor (NNRTI) rilpivirine (RPV) is indicated for human immunodeficiency virus type-1 (HIV-1) patients initiating antiretroviral treatment, but the extent of genotypic RPV resistance in treatment-naive patients outside clinical trials is poorly defined. Study Design: This retrospective observational study of clinical data from Belgium and Portugal evaluates genotypic information from HIV-1 drug-naive patients obtained for the purpose of drug resistance testing. Rilpivirine resistance-associated mutations (RPV-RAMs) were defined based on clinical trials, phenotypic studies, and expert-based resistance algorithms. Viral susceptibility to RPV alone and to the single-tablet regimen was estimated using expert-based resistance algorithms. Results: In 4,631 HIV-1 treatment-naive patients infected with diverse HIV-1 subtypes, major RPV-RAMs were detected in 4.6%, while complete viral susceptibility to RPV was estimated in 95% of patients. Subtype C- and F1-infected patients displayed the highest levels of reduced viral susceptibility at baseline, respectively 13.2% and 9.3%, mainly due to subtype- and geographic-dependent occurrence of RPV-RAMs E138A and A98G as natural polymorphisms. Strikingly, a founder effect in Portugal resulted in a 138A prevalence of 13.2% in local subtype C-infected treatment-naive patients. The presence of transmitted drug resistance did not impact our estimates. Conclusion: RPV is the first HIV-1 inhibitor for which, in the absence of transmitted drug resistance, intermediate or high-level genotypic resistance can be detected in treatment-naive patients. The extent of RPV susceptibility in treatment-naive patients differs depending on the HIV-1 subtype and dynamics of local compartmentalized epidemics. The highest prevalence of reduced susceptibility was found to be 15.7% in Portuguese subtype C-infected treatment-naive patients. In this context, even in the absence of transmitted HIV-1 drug resistance (TDR), drug resistance testing ...