Thu Huynh Hoang Khanh, Schemelev Alexandr N, Ostankova Yulia V, Davydenko Vladimir S, Reingardt Diana E, Tran Ton, Thanh Le Chi, Truong Thi Xuan Lien, Totolian Areg A
Pasteur Institute in Ho Chi Minh City, Ho Chi Minh City 70000, Vietnam.
Saint Petersburg Pasteur Institute, St. Petersburg 197101, Russia.
Diagnostics (Basel). 2025 May 18;15(10):1279. doi: 10.3390/diagnostics15101279.
Vietnam has made significant strides in reducing the prevalence of HIV infection and achievements in its antiretroviral treatment program. However, the COVID-19 pandemic and financial challenges in the healthcare system have posed significant obstacles to maintaining effective HIV treatment and monitoring, particularly among vulnerable populations. This study aims to evaluate the situation of HIV drug resistance among patients who have experienced treatment failure in the Mekong Delta region and to compare data from 2019 to 2022. The study material was blood plasma samples from HIV-infected individuals with ART failure: 316 collected in 2019 and 326 collected in 2022. HIV-1 genotyping and mutation detection were performed based on an analysis of the nucleotide sequences of the gene region. A total of 116 HIV-infected individuals with virological failure in 2019 and 2022 were assessed for HIV drug resistance. The study revealed a high proportion of participants with viral loads exceeding 1000 copies/mL, significantly increasing from 12.0% in 2019 to 23.9% in 2022 (OR = 2.3; = 0.0001). HIV drug resistance mutations were detected in 84.21% of cases in 2019 and 92.59% in 2022. The prevalence of concurrent resistance to NRTIs and NNRTIs was 37.5% and 30.13% in 2019 and 2022, respectively. There was a statistically significant decrease in NNRTI resistance (OR = 0.32, χ = 5.43, < 0.05). In contrast, multi-drug resistance to protease inhibitors rose from 18.52% to 45.21% (φ* = 0.00403, < 0.05). Triple-class resistance was identified only in 2022 (17.81%). The most common mutations included M184I/V, D67N, K103N, Y181C, and V82A/S/T, with D67N rising significantly from 3.13% to 21.92%. The predominant subtype was CRF01_AE. A high prevalence of viral non-suppression and HIV drug resistance was observed among patients in the Mekong Delta region, particularly after the onset of the COVID-19 pandemic. Our study highlights the ongoing challenges that the HIV/AIDS treatment program in Vietnam must address in the post-pandemic period to sustain its success and achieve the goals of the country's HIV prevention strategies.
越南在降低艾滋病毒感染率方面取得了重大进展,其抗逆转录病毒治疗计划也取得了成效。然而,新冠疫情和医疗系统面临的财政挑战给维持有效的艾滋病毒治疗和监测带来了重大障碍,尤其是在弱势群体中。本研究旨在评估湄公河三角洲地区治疗失败患者的艾滋病毒耐药情况,并比较2019年至2022年的数据。研究材料为抗逆转录病毒治疗失败的艾滋病毒感染者的血浆样本:2019年收集了316份,2022年收集了326份。基于对该基因区域核苷酸序列的分析进行艾滋病毒-1基因分型和突变检测。对2019年和2022年共116例病毒学失败的艾滋病毒感染者进行了艾滋病毒耐药性评估。研究显示,病毒载量超过1000拷贝/毫升的参与者比例很高,从2019年的12.0%显著增至2022年的23.9%(比值比=2.3;P=0.0001)。2019年84.21%的病例和2022年92.59%的病例检测到艾滋病毒耐药突变。2019年和2022年,对核苷类逆转录酶抑制剂和非核苷类逆转录酶抑制剂同时耐药的患病率分别为37.5%和30.13%。非核苷类逆转录酶抑制剂耐药性有统计学显著下降(比值比=0.32,χ²=5.43,P<0.05)。相比之下,对蛋白酶抑制剂的多药耐药性从18.52%升至45.21%(φ*=0.00403,P<0.05)。仅在2022年发现了三重耐药(17.81%)。最常见的突变包括M184I/V、D67N、K103N、Y181C和V82A/S/T,其中D67N从3.13%显著升至21.92%。主要亚型为CRF01_AE。在湄公河三角洲地区的患者中观察到病毒抑制不佳和艾滋病毒耐药的高患病率,尤其是在新冠疫情爆发后。我们的研究突出了越南艾滋病毒/艾滋病治疗计划在疫情后时期为维持其成功并实现该国艾滋病毒预防战略目标必须应对的持续挑战。