OBJECTIVES: To investigate mutations selected in viruses from HIV-2-infected patients failing a highly active antiretroviral treatment (HAART) regimen including atazanavir/ritonavir. METHODS: Twenty-eight HIV-2-infected patients previously exposed to atazanavir/ritonavir and failing therapy were studied. The protease (PR) gene was amplified and sequenced, and mutations emerging under atazanavir/ritonavir selective pressure were reported. RESULTS: The I50L mutation emerged in 4 out of 28 HIV-2-infected patients failing a HAART regimen including atazanavir/ritonavir. Besides I50L, four PR mutations previously associated with protease inhibitor resistance (I54L, I64V, V71I and I82F) and six PR mutations of unknown impact (V10I, E37D, S43T, K45...
Background: To estimate to what extent darunavir might be effective in patients failing distinct pro...
Objective: This study aims to investigate the prevalence and types of drug resistance mutations amon...
2 The spectrum of HIV-1 protease and reverse transcriptase (RT) mutations selected by antiretroviral...
Objectives: To determine protease mutations that develop at viral failure for protease inhibitor (PI...
ObjectivesTo determine protease mutations that develop at viral failure for protease inhibitor (PI)-...
Ritonavir-boosted atazanavir is an option for second-line therapy in low- and middle-income countrie...
Ritonavir‐boosted atazanavir is an option for second‐line therapy in low‐ and middle-income countrie...
Background: HIV-1 and HIV-2 differ in their antiretroviral (ARV) susceptibilities and drug resistanc...
OBJECTIVES: The aim of this retrospective study was to evaluate treatment outcome and characterize t...
OBJECTIVES: The protease inhibitor atazanavir (ATV) can be used either boosted by ritonavir (ATV300/...
Raltegravir is highly efficacious in the treatment of HIV-1 infection. The prevalence and impact on ...
OBJECTIVES: This study evaluates the impact of specific HIV-1 protease-compensatory mutations (wild-...
OBJECTIVE: To assess the prevalence of mutations in the reverse-transcriptase (RT) and protease (PR)...
Objectives: To search for genetic factors in the protease and gag regions (NC-p1/TFP-p6/p6pol) invol...
Raltegravir is highly efficacious in the treatment of HIV-1 infection. The prevalence and impact on ...
Background: To estimate to what extent darunavir might be effective in patients failing distinct pro...
Objective: This study aims to investigate the prevalence and types of drug resistance mutations amon...
2 The spectrum of HIV-1 protease and reverse transcriptase (RT) mutations selected by antiretroviral...
Objectives: To determine protease mutations that develop at viral failure for protease inhibitor (PI...
ObjectivesTo determine protease mutations that develop at viral failure for protease inhibitor (PI)-...
Ritonavir-boosted atazanavir is an option for second-line therapy in low- and middle-income countrie...
Ritonavir‐boosted atazanavir is an option for second‐line therapy in low‐ and middle-income countrie...
Background: HIV-1 and HIV-2 differ in their antiretroviral (ARV) susceptibilities and drug resistanc...
OBJECTIVES: The aim of this retrospective study was to evaluate treatment outcome and characterize t...
OBJECTIVES: The protease inhibitor atazanavir (ATV) can be used either boosted by ritonavir (ATV300/...
Raltegravir is highly efficacious in the treatment of HIV-1 infection. The prevalence and impact on ...
OBJECTIVES: This study evaluates the impact of specific HIV-1 protease-compensatory mutations (wild-...
OBJECTIVE: To assess the prevalence of mutations in the reverse-transcriptase (RT) and protease (PR)...
Objectives: To search for genetic factors in the protease and gag regions (NC-p1/TFP-p6/p6pol) invol...
Raltegravir is highly efficacious in the treatment of HIV-1 infection. The prevalence and impact on ...
Background: To estimate to what extent darunavir might be effective in patients failing distinct pro...
Objective: This study aims to investigate the prevalence and types of drug resistance mutations amon...
2 The spectrum of HIV-1 protease and reverse transcriptase (RT) mutations selected by antiretroviral...