Murphy Richard A, Bedesi Pradeep H, Perumal Nirmala, Gosnell Bernadett I, Hatlen Timothy J, Brijkumar Jaysingh
Division of Infectious Diseases, Geisel School of Medicine at Dartmouth, Hanover, New Hampshire, USA.
Division of Infectious Diseases, White River Junction Veterans Affairs Medical Center, White River Junction, Vermont, USA.
Open Forum Infect Dis. 2024 Jun 5;11(7):ofae321. doi: 10.1093/ofid/ofae321. eCollection 2024 Jul.
Dolutegravir resistance is emerging in routine clinical contexts in southern Africa, primarily in patients with prior treatment experience failing dolutegravir-based antiretroviral therapy (ART). This potential issue was raised by The Nucleosides and Darunavir/Dolutegravir in Africa trial that compared dolutegravir and boosted protease inhibitor-based therapy as second-line ART, in which new dolutegravir resistance was observed at failure. However, recent data suggest that also at risk are patients who were transitioned to dolutegravir from non-nucleoside reverse transcriptase inhibitor-based ART while viremic. Identifying patients experiencing failure of dolutegravir with resistance will be difficult given current gaps in viral load monitoring and limited capacity for genotypic resistance testing. As a result, in the short term, most patients affected will go unrecognized, with particularly important implications for patients affected who have advanced HIV or who are pregnant/breastfeeding. Prospective research is needed to understand the scope of the problem, identify additional risk factors, and determine best management. In the short term, for most patients with dolutegravir resistance and prior non-nucleoside reverse transcriptase inhibitor exposure, the best option will be a timely switch to a regimen anchored by a boosted protease inhibitor, with a high genetic barrier to resistance.
在非洲南部的常规临床环境中,多替拉韦耐药性正在出现,主要发生在既往接受过以多替拉韦为基础的抗逆转录病毒疗法(ART)但治疗失败的患者中。《非洲核苷类药物与达芦那韦/多替拉韦试验》提出了这一潜在问题,该试验比较了多替拉韦与强化蛋白酶抑制剂为基础的疗法作为二线ART,其中在治疗失败时观察到了新的多替拉韦耐药性。然而,最近的数据表明,病毒血症患者从基于非核苷类逆转录酶抑制剂的ART转换为多替拉韦时也面临风险。鉴于目前病毒载量监测存在差距以及基因型耐药性检测能力有限,识别出现多替拉韦耐药性失败的患者将很困难。因此,在短期内,大多数受影响的患者将未被识别,这对患有晚期HIV或怀孕/哺乳的受影响患者具有特别重要的意义。需要进行前瞻性研究以了解问题的范围,识别其他风险因素,并确定最佳管理方法。短期内,对于大多数有多替拉韦耐药性且既往暴露于非核苷类逆转录酶抑制剂的患者,最佳选择将是及时转换为以强化蛋白酶抑制剂为基础的方案,该方案具有较高的耐药基因屏障。