Department of Infectious Diseases and Hospital Epidemiology, University Hospital Zurich, Zurich, Switzerland; Institute of Medical Virology, University of Zurich, Zurich, Switzerland.
Institute of Social and Preventive Medicine (ISPM), University of Bern, Bern, Switzerland.
Lancet HIV. 2023 Nov;10(11):e733-e741. doi: 10.1016/S2352-3018(23)00228-X. Epub 2023 Oct 10.
The widespread use of the integrase strand transfer inhibitor (INSTI) dolutegravir in first-line and second-line antiretroviral therapy (ART) might facilitate emerging resistance. The DTG RESIST study combined data from HIV cohorts to examine patterns of drug resistance mutations (DRMs) and identify risk factors for dolutegravir resistance.
We included cohorts with INSTI resistance data from two collaborations (ART Cohort Collaboration, International epidemiology Databases to Evaluate AIDS in Southern Africa), and the UK Collaborative HIV Cohort. Eight cohorts from Canada, France, Germany, Italy, the Netherlands, Switzerland, South Africa, and the UK contributed data on individuals who were viraemic on dolutegravir-based ART and underwent genotypic resistance testing. Individuals with unknown dolutegravir initiation date were excluded. Resistance levels were categorised using the Stanford algorithm. We identified risk factors for resistance using mixed-effects ordinal logistic regression models.
We included 599 people with genotypic resistance testing on dolutegravir-based ART between May 22, 2013, and Dec 20, 2021. Most had HIV-1 subtype B (n=351, 59%), a third had been exposed to first-generation INSTIs (n=193, 32%), 70 (12%) were on dolutegravir dual therapy, and 18 (3%) were on dolutegravir monotherapy. INSTI DRMs were detected in 86 (14%) individuals; 20 (3%) had more than one mutation. Most (n=563, 94%) were susceptible to dolutegravir, seven (1%) had potential low, six (1%) low, 17 (3%) intermediate, and six (1%) high-level dolutegravir resistance. The risk of dolutegravir resistance was higher on dolutegravir monotherapy (adjusted odds ratio [aOR] 34·1, 95% CI 9·93-117) and dolutegravir plus lamivudine dual therapy (aOR 9·21, 2·20-38·6) compared with combination ART, and in the presence of potential low or low (aOR 5·23, 1·32-20·7) or intermediate or high-level (aOR 13·4, 4·55-39·7) nucleoside reverse transcriptase inhibitor (NRTI) resistance.
Among people with viraemia on dolutegravir-based ART, INSTI DRMs and dolutegravir resistance were rare. NRTI resistance substantially increased the risk of dolutegravir resistance, which is of concern, notably in resource-limited settings. Monitoring is important to prevent resistance at the individual and population level and ensure the long-term sustainability of ART.
US National Institutes of Health, Swiss National Science Foundation.
整合酶链转移抑制剂(INSTI)多替拉韦在一线和二线抗逆转录病毒治疗(ART)中的广泛应用可能会促进新的耐药性的出现。DTG RESIST 研究结合了 HIV 队列的数据,以检查耐药突变(DRMs)的模式,并确定对多替拉韦耐药的风险因素。
我们纳入了来自两个合作组织(ART 队列合作组织、南部非洲国际艾滋病流行病学数据库)和英国合作 HIV 队列的 INSTI 耐药数据的队列,并纳入了来自加拿大、法国、德国、意大利、荷兰、瑞士、南非和英国的八个队列的数据,这些队列中的个体在基于多替拉韦的 ART 中病毒血症,并进行了基因型耐药性检测。排除了不知道多替拉韦起始日期的个体。使用斯坦福算法对耐药水平进行分类。我们使用混合效应有序逻辑回归模型确定耐药的风险因素。
我们纳入了 599 名在 2013 年 5 月 22 日至 2021 年 12 月 20 日期间接受基于多替拉韦的 ART 治疗并进行了基因型耐药性检测的个体。大多数人 HIV-1 亚型为 B(n=351,59%),三分之一的人曾接触过第一代 INSTIs(n=193,32%),70 人(12%)接受多替拉韦双联治疗,18 人(3%)接受多替拉韦单药治疗。在 86 名个体(14%)中检测到 INSTI DRMs;20 人(3%)有一个以上的突变。大多数(n=563,94%)对多替拉韦敏感,7 人(1%)有潜在低、6 人(1%)低、17 人(3%)中、6 人(1%)高水平多替拉韦耐药。与联合 ART 相比,多替拉韦单药治疗(调整后的优势比[aOR]34.1,95%CI 9.93-117)和多替拉韦加拉米夫定双联治疗(aOR 9.21,2.20-38.6)的多替拉韦耐药风险更高,而潜在低或低(aOR 5.23,1.32-20.7)或中或高水平(aOR 13.4,4.55-39.7)核苷逆转录酶抑制剂(NRTI)耐药时耐药风险更高。
在接受多替拉韦为基础的 ART 病毒血症的人群中,INSTI DRMs 和多替拉韦耐药性罕见。NRTI 耐药显著增加了多替拉韦耐药的风险,这令人担忧,尤其是在资源有限的环境中。监测对于防止个体和人群水平的耐药性以及确保 ART 的长期可持续性非常重要。
美国国立卫生研究院,瑞士国家科学基金会。