首页> 美国卫生研究院文献>BMC Research Notes >Virological response HIV-1 drug resistance mutations and genetic diversity among patients on first-line antiretroviral therapy in N’Djamena Chad: findings from a cross-sectional study
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Virological response HIV-1 drug resistance mutations and genetic diversity among patients on first-line antiretroviral therapy in N’Djamena Chad: findings from a cross-sectional study

机译:乍得内贾梅纳一线抗逆转录病毒疗法患者的病毒学应答HIV-1耐药性突变和遗传多样性:一项横断面研究的结果

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摘要

BackgroundThe national antiretroviral therapy in the Republic of Chad provides free of charge antiretroviral regimens and therapeutic monitoring for patients receiving antiretroviral therapy nationwide. For a successful programmatic uptake, these efforts merit to be supported by thorough assessments of antiretroviral therapy response and HIV-1 drug resistance surveillance, especially with risks of cross-resistance due to the gradual stavudine phasing out in such national settings. We therefore evaluated the virological response to antiretroviral therapy, HIV-1 drug resistance emergence and circulating HIV-1 clades in a Chad context. A cross-sectional and prospective study was conducted among 116 patients (41 [δ ± 6.87] years, 59% female) receiving first-line antiretroviral therapy for ≥ 6 months in Ndjamena, Chad, in 2011–2012, enrolled consecutively. To ensure accuracy, plasma viral load was concomitantly measured using Abbott Real-Time and Cobas AmpliPrep/TaqMan (v2.0), and virological failure defined as ≥ 1000 HIV-1 RNA copies/ml. Plasma from patients experiencing virological failure were processed for sequencing of HIV-1 protease-reverse transcriptase using the ANRS-AC.11 resistance testing protocol; drug resistant mutations were interpreted using the ANRS-AC11 algorithm; and phylogenetic analysis was performed using MEGA.v.6.
机译:背景乍得共和国的国家抗逆转录病毒疗法为全国接受抗逆转录病毒疗法的患者提供免费的抗逆转录病毒疗法和治疗监测。为了成功地通过计划实施,这些工作应得到对抗逆转录病毒疗法反应和HIV-1耐药性监测的全面评估的支持,特别是由于在这样的国家环境中逐步淘汰司他夫定具有交叉耐药性的风险。因此,我们在乍得背景下评估了对抗逆转录病毒疗法,HIV-1耐药性出现和循环HIV-1进化枝的病毒学反应。于2011-2012年在乍得的恩贾梅纳连续接受了≥6个月的一线抗逆转录病毒治疗的116例患者(41 [δ±6.87]岁,女性59%)进行了横断面和前瞻性研究。为确保准确性,同时使用Abbott Real-Time和Cobas AmpliPrep / TaqMan(v2.0)测量血浆病毒载量,并将病毒学衰竭定义为≥1000 HIV-1 RNA拷贝/ ml。使用ANRS-AC.11耐药性测试规程,对来自病毒学衰竭患者的血浆进行HIV-1蛋白酶逆转录酶测序。使用ANRS-AC11算法解释了耐药性突变;并使用MEGA.v.6进行了系统发育分析。

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