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人类免疫缺陷病毒 1 型整合酶链转移抑制剂的疗效和耐药性的荟萃分析和系统评价。

Meta-analysis and systematic review of the efficacy and resistance for human immunodeficiency virus type 1 integrase strand transfer inhibitors.

机构信息

Institute of Drug Metabolism and Pharmaceutical Analysis, College of Pharmaceutical Sciences, Zhejiang University, No. 866 Yuhangtang Road, Hangzhou 310058, China.

Department of Nephrology, Central Hospital of Zibo, Zibo 255020, China.

出版信息

Int J Antimicrob Agents. 2019 Nov;54(5):547-555. doi: 10.1016/j.ijantimicag.2019.08.008. Epub 2019 Aug 6.

Abstract

Integrase strand transfer inhibitors (INSTIs) are the most recent class of antiretroviral drugs with potent and durable antiviral activity used to treat human immunodeficiency virus type 1 (HIV-1) infection. However, development of drug resistance increases the risk of treatment failure, disease progression and mortality. A better understanding of drug efficacy and resistance against INSTIs is crucial for their efficient use and the development of new antiretrovirals. A meta-analysis of studies reporting efficacy and resistance data on INSTI use in HIV-infected patients was performed. Odds ratios (ORs) of efficacy outcome data favouring INSTI use in different clinical settings demonstrated that INSTIs have higher efficacy compared with drugs of other classes. For combination antiretroviral therapy-naïve patients and virologically-suppressed patients who switched to INSTI-based therapy, the OR was 1.484 (95% CI 1.229-1.790) and 1.341 (95% CI 0.913-1.971), respectively. ORs of resistance data indicated decreased treatment-emergent resistance development to dolutegravir (DTG) upon virological failure than to non-INSTIs (OR = 0.081, 95% CI 0.004-1.849), whereas the opposite was observed for raltegravir (RAL) (OR = 3.137, 95% CI 1.827-5.385) and elvitegravir (EVG) (OR = 1.886, 95% CI 0.569-6.252). Pooled analysis of resistance data indicated that development of resistance to DTG and bictegravir was rare, whereas EVG and RAL had low genetic barriers to resistance and the intensive cross-resistance between them limits INSTI efficiency. Efficient means of monitoring the emergence of resistance to INSTIs and the development of drugs with high genetic barriers are clear paths for future research.

摘要

整合酶链转移抑制剂(INSTIs)是最新的一类抗逆转录病毒药物,具有强大而持久的抗病毒活性,用于治疗人类免疫缺陷病毒 1 型(HIV-1)感染。然而,耐药性的发展增加了治疗失败、疾病进展和死亡的风险。更好地了解药物疗效和对 INSTIs 的耐药性对于它们的有效使用和新抗逆转录病毒药物的开发至关重要。对报告 INSTI 治疗 HIV 感染患者的疗效和耐药性数据的研究进行了荟萃分析。在不同临床环境下使用 INSTI 的疗效数据的优势比(OR)表明,INSTIs 比其他类别的药物具有更高的疗效。对于初治和病毒学抑制的患者转换为 INSTI 治疗的患者,OR 分别为 1.484(95%CI 1.229-1.790)和 1.341(95%CI 0.913-1.971)。耐药数据的 OR 表明,在病毒学失败时,与非 INSTIs 相比,发展替拉格瑞韦(DTG)的治疗后耐药的发生率降低(OR=0.081,95%CI 0.004-1.849),而拉替格瑞韦(RAL)(OR=3.137,95%CI 1.827-5.385)和艾维雷韦(EVG)(OR=1.886,95%CI 0.569-6.252)则相反。耐药数据的汇总分析表明,对 DTG 和比克替拉韦耐药的发展很少见,而 EVG 和 RAL 对耐药的遗传屏障较低,它们之间的广泛交叉耐药限制了 INSTI 的效率。监测 INSTI 耐药性出现和开发具有高遗传屏障的药物的有效方法是未来研究的明确方向。

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