Tenofovir disoproxil fumarate (TDF) genotypic resistance defined by K65R/N and/ or K70E/Q/G occurs in 20% to 60% of individuals with virological failure (VF) on aWHO-recommended TDF-containing first-line regimen. However, the full spectrumof reverse transcriptase (RT) mutations selected in individuals with VF on such a regimen is not known. To identify TDF regimen-associated mutations (TRAMs), we compared the proportion of each RT mutation in 2873 individuals with VF on a WHO-recommended first-line TDF-containing regimen to its proportion in a cohort of 50,803 antiretroviral-naive individuals. To identify TRAMs specifically associatedwith TDF-selection pressure, we compared the proportion of each TRAMto its proportion in a cohort of 5805 individuals with VF on a first-line thymidine analog-containing regimen. We identified 83 TRAMs including 33 NRTI-associated, 40 NNRTI-associated, and 10 uncommon mutations of uncertain provenance. Of the 33 NRTI-associated TRAMs, 12-A62V, K65R/N, S68G/N/D, K70E/Q/T, L74I, V75L, and Y115F -weremore common among individuals receiving a first-line TDF-containing compared to a first-line thymidine analog-containing regimen. These 12 TDF-selected TRAMswill be important formonitoring TDF-associated transmitted drug-resistance and for determining the extent of reduced TDF susceptibility in individuals with VF on a TDF-containing regimen. (C) 2017 The Authors. Published by Elsevier B. V.

Rhee, S.-., Varghese, V., Holmes, S.p., Van Zyl, G.u., Steegen, K., Boyd, M.a., et al. (2017). Mutational Correlates of Virological Failure in Individuals Receiving a WHO-Recommended Tenofovir-Containing First-Line Regimen: An International Collaboration. EBIOMEDICINE, 18, 225-235 [10.1016/j.ebiom.2017.03.024].

Mutational Correlates of Virological Failure in Individuals Receiving a WHO-Recommended Tenofovir-Containing First-Line Regimen: An International Collaboration

Santoro M.;
2017-01-01

Abstract

Tenofovir disoproxil fumarate (TDF) genotypic resistance defined by K65R/N and/ or K70E/Q/G occurs in 20% to 60% of individuals with virological failure (VF) on aWHO-recommended TDF-containing first-line regimen. However, the full spectrumof reverse transcriptase (RT) mutations selected in individuals with VF on such a regimen is not known. To identify TDF regimen-associated mutations (TRAMs), we compared the proportion of each RT mutation in 2873 individuals with VF on a WHO-recommended first-line TDF-containing regimen to its proportion in a cohort of 50,803 antiretroviral-naive individuals. To identify TRAMs specifically associatedwith TDF-selection pressure, we compared the proportion of each TRAMto its proportion in a cohort of 5805 individuals with VF on a first-line thymidine analog-containing regimen. We identified 83 TRAMs including 33 NRTI-associated, 40 NNRTI-associated, and 10 uncommon mutations of uncertain provenance. Of the 33 NRTI-associated TRAMs, 12-A62V, K65R/N, S68G/N/D, K70E/Q/T, L74I, V75L, and Y115F -weremore common among individuals receiving a first-line TDF-containing compared to a first-line thymidine analog-containing regimen. These 12 TDF-selected TRAMswill be important formonitoring TDF-associated transmitted drug-resistance and for determining the extent of reduced TDF susceptibility in individuals with VF on a TDF-containing regimen. (C) 2017 The Authors. Published by Elsevier B. V.
2017
Pubblicato
Rilevanza internazionale
Articolo
Esperti anonimi
Settore MED/07 - MICROBIOLOGIA E MICROBIOLOGIA CLINICA
English
Antiretroviral therapy; Drug resistance; HIV-1; Reverse transcriptase; Tenofovir; WHO-recommended first-line; Drug Resistance, Viral; Genotype; HIV Infections; HIV Reverse Transcriptase; HIV-1; Humans; Mutation; Prevalence; Reverse Transcriptase Inhibitors; Tenofovir; Treatment Failure; Viral Load; World Health Organization
Rhee, S.-., Varghese, V., Holmes, S.p., Van Zyl, G.u., Steegen, K., Boyd, M.a., et al. (2017). Mutational Correlates of Virological Failure in Individuals Receiving a WHO-Recommended Tenofovir-Containing First-Line Regimen: An International Collaboration. EBIOMEDICINE, 18, 225-235 [10.1016/j.ebiom.2017.03.024].
Rhee, S-; Varghese, V; Holmes, Sp; Van Zyl, Gu; Steegen, K; Boyd, Ma; Cooper, Da; Nsanzimana, S; Saravanan, S; Charpentier, C; de Oliveira, T; Etiebet, M-A; Garcia, F; Goedhals, D; Gomes, P; Gunthard, Hf; Hamers, Rl; Hoffmann, Cj; Hunt, G; Jiamsakul, A; Kaleebu, P; Kanki, P; Kantor, R; Kerschberger, B; Marconi, Vc; D'amour Ndahimana, J; Ndembi, N; Ngo-Giang-Huong, N; Rokx, C; Santoro, M; Schapiro, Jm; Schmidt, D; Seu, L; Sigaloff, Kce; Sirivichayakul, S; Skhosana, L; Sunpath, H; Tang, M; Yang, C; Carmona, S; Gupta, Rk; Shafer, Rw
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2108/243384
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