作者: Michael Maguire , Martin Gartland , Sarah Moore , Andrew Hill , Margaret Tisdale
DOI: 10.1097/00002030-200006160-00017
关键词: Resistance mutation 、 Lamivudine 、 Drug resistance 、 Protease inhibitor (pharmacology) 、 Zidovudine 、 Population 、 Indinavir 、 Nelfinavir 、 Medicine 、 Virology
摘要: Objectives To assess the role of resistance mutations in subjects experiencing virological failure on zidovudine (ZDV) and lamivudine (3TC) combined with a protease inhibitor (PI) to those failing ZDV/3TC alone. Design methods Samples were obtained from previously antiretroviral therapy-naive enrolled into two studies, AVANTI 2 3. Subjects randomized receive either: or plus indinavir (IDV) for 52 weeks (AVANTI 2), nelfinavir (NFV) 28 3). Emergence viral was monitored by population sequencing phenotypic determined recombinant virus assay. Results Genotypic data plasma HIV-1 RNA > 400 copies/ml. In 2, ZDV detected 27% ZDV/3TC-treated patients at week 52, but absent treated ZDV/3TC/IDV. No either arm 3 developed 28. The M184V mutation most both studies. presence was, however, associated significantly lower RNA levels when compared values before initiation treatment. There high frequency (4 11) L10F substitution ZDV/3TC/IDV-treated that did not result any PIs tested. Conclusions ZDV/3TC/PI-treated they slowly ZDV/3TC. Few known confer PI ZDV/3TC/PI arms study. low prevalence is encouraging regarding future treatment options these patients.