首页> 外文期刊>The Journal of Infectious Diseases >Low-frequency nevirapine (NVP)-resistant HIV-1 variants are not associated with failure of antiretroviral therapy in women without prior exposure to single-dose NVP
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Low-frequency nevirapine (NVP)-resistant HIV-1 variants are not associated with failure of antiretroviral therapy in women without prior exposure to single-dose NVP

机译:耐奈韦拉平(NVP)的低频HIV-1变异与未事先暴露于单剂量NVP的女性的抗逆转录病毒治疗失败无关

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Background. Low-frequency nevirapine (NVP)-resistant variants have been associated with virologic failure (VF) of initial NVP-based combination antiretroviral therapy (cART) in women with prior exposure to single-dose NVP (sdNVP). We investigated whether a similar association exists in women without prior sdNVP exposure.Methods. Pre-cART plasma was analyzed by allele-specific polymerase chain reaction to quantify NVP-resistant mutants in human immunodeficiency virus-infected African women without prior sdNVP who were starting first-line NVP-based cART in the OCTANE/A5208 trial 2. Associations between NVP-resistant mutants and VF or death were determined and compared with published results from women participating in the OCTANE/A5208 trial 1 who had taken sdNVP and initiated NVP-based cART.Results. Pre-cART NVP-resistant variants were detected in 18% (39/219) of women without prior sdNVP exposure, compared to 45% (51/114) with prior sdNVP exposure (P <. 001). Among women without prior sdNVP exposure, 8 of 39 (21%) with NVP-resistant variants experienced VF or death vs 31 of 180 (17%) without such variants (P =. 65); this compares with 21 of 51 (41%) vs 9 of 63 (14%) among women with prior exposure (P =. 001).Conclusions. The risk of VF on NVP-based cART from NVP-resistant variants differs between sdNVP-exposed and-unexposed women. This difference may be driven by drug-resistance mutations emerging after sdNVP exposure that are linked on the same viral genome.
机译:背景。先前接受单剂量NVP(sdNVP)的女性中,低频奈韦拉平(NVP)耐药变异与最初基于NVP的联合抗逆转录病毒疗法(cART)的病毒学衰竭(VF)相关。我们调查了在没有sdNVP暴露的女性中是否存在类似的关联。通过等位基因特异性聚合酶链反应分析了pre-cART血浆,以定量人类免疫缺陷病毒感染的非洲女性中没有sdNVP的耐NVP突变体,这些女性在OCTANE / A5208试验2中开始基于NVP的一线研究。确定了耐NVP的突变体和VF或死亡,并将其与参加OCTAE / A5208试验1的妇女的已发表结果进行了比较,这些妇女服用了sdNVP并启动了基于NVP的cART。未接触sdNVP的女性中有18%(39/219)的女性检测到了前cART NVP耐药变异,而之前接触sdNVP的女性中有45%(51/114)(P <.001)。在没有sdNVP暴露的女性中,有NVP耐药变异的39名女性中有8名(21%)经历了室颤或死亡,而没有此类变异的180名女性中有31名(17%)经历了VF或死亡(P = 65)。相比之下,先前有过接触的女性中有21人(占41%)(41%)与63人中的9%(14%)相比(P = .001)。暴露于sdNVP的女性和未暴露于sdNVP的女性在基于NVP的基于NVP的cART上发生VF的风险不同。这种差异可能是由sdNVP暴露后出现在同一病毒基因组上的耐药性突变驱动的。

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