Department of Medicine, Institute of Medical Sciences, Banaras Hindu University, Varanasi, India.
Am J Trop Med Hyg. 2024 Mar 5;110(4):713-718. doi: 10.4269/ajtmh.23-0026. Print 2024 Apr 3.
India has the third-largest number of people living with HIV (PLHIV) in the world. A national program provides free access to standard uniform antiretroviral therapy. However, the program is not monitored by comprehensive drug resistance surveys. The aim of this study was to determine the prevalence of HIV drug resistance mutations (DRMs) among treatment-naive PLHIV in a large antiretroviral treatment center of the national program. This cross-sectional study was done in 2017 and involved 200 consecutive treatment-naive PLHIV. A target fragment of 1,306 bp in the reverse transcriptase and protease regions was amplified. Identification of mutations and drug resistance interpretation was done by HIV Genotypic Resistance Interpretation and International Antiviral Society-USA list. Sequencing was successful in 177 samples. The majority (98.8%; 175/177) belonged to subtype C. Nineteen of 177 patients (10.7%; 95% CI: 6.2%-15.3%) had at least one major DRM. The prevalence of non-nucleoside reverse transcriptase inhibitor (NNRTI) mutations was 10.2% (18/177). The most frequent mutations were E138A/K, A98G, K103N, V179D, and K101H/E. The prevalence of nucleoside reverse transcriptase inhibitor (NRTI) mutations was 1.1% (2/177). None of the samples had major protease inhibitor resistance mutations. The prevalence of NNRTI mutations in this study was >10%, crossing the threshold recommended by the WHO to change the NNRTI-based first-line regimen to non-NNRTI based. In 2021, the national program replaced efavirenz with dolutegravir in the first-line regimen of tenofovir, lamivudine, and efavirenz. As the majority (64%) of PLHIV in India are accessing free ART from the national program, this study highlights the need for regular nationally representative drug resistance surveys for optimizing antiretroviral regimens in the program.
印度是世界上艾滋病毒感染者(PLHIV)人数第三多的国家。国家项目提供免费的标准统一抗逆转录病毒治疗。然而,该项目并未通过全面的耐药性调查进行监测。本研究的目的是在国家项目的一个大型抗逆转录病毒治疗中心确定初治 PLHIV 中 HIV 耐药突变(DRMs)的流行率。这项横断面研究于 2017 年进行,涉及 200 名连续初治 PLHIV。扩增逆转录酶和蛋白酶区域的 1306 个碱基对的靶片段。通过 HIV 基因型耐药性解释和国际抗病毒学会-美国列表进行突变和耐药性的鉴定。177 个样本中测序成功。大多数(98.8%;175/177)属于 C 亚型。177 例患者中有 19 例(10.7%;95%CI:6.2%-15.3%)至少有一种主要的耐药突变。非核苷类逆转录酶抑制剂(NNRTI)突变的患病率为 10.2%(18/177)。最常见的突变是 E138A/K、A98G、K103N、V179D 和 K101H/E。核苷类逆转录酶抑制剂(NRTI)突变的患病率为 1.1%(2/177)。没有样本有主要的蛋白酶抑制剂耐药突变。本研究中 NNRTI 突变的患病率>10%,超过了世界卫生组织推荐的将基于 NNRTI 的一线方案改为基于非-NNRTI 的方案的阈值。2021 年,国家项目在替诺福韦、拉米夫定和依非韦伦的一线方案中用度鲁特韦代替了依非韦伦。由于印度 64%的 PLHIV 正在从国家项目中获得免费的 ART,因此本研究强调需要定期进行全国代表性的耐药性调查,以优化该项目中的抗逆转录病毒方案。