Checking the Status: The Evolutionary Explanations and Drug Resistance Prevalence to Dolutegravir for HIV Treatment (A Review)

Evan Hall
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Abstract

Drug treatment advancements for HIV have dramatically advanced since the virus’ identification in the early 1980s. Integrase strand transfer inhibitors (INSTIs) are one of seven HIV treatment drug classes currently utilized to create an undetectable viral count in blood samples of people living with HIV (PLWH). First generation INSTIs are documented with low barriers of genetic resistance, which indicates that the number of mutations to lead to a drug resistant mutation is low. The introduction of dolutegravir, a second generation INSTI, shows a higher barrier of genetic resistance that will reduce drug resistant mutations to INSTIs and increase the overall effectiveness of this class of HIV treatment. PLWH can be categorized based on whether they received treatment previously/currently or have never received treatment. Therapy naive and previously treated (successfully or unsuccessfully) patients for HIV report different rates of drug resistant mutations compared to actual resistance to dolutegravir, 0.4-31% and 0.1-67.2% respectively. Evolutionary considerations of genetic resistance, including epistatic interactions and point mutations, suggest both non-polymorphic and polymorphic mutations for these drug resistant mutations. An incomplete understanding of how evolutionary factors contribute to HIV drug resistance highlights the importance of conducting further research. This research may help improve the efficacy of second generation INSTIs in future treatment options for PLWH. This review describes the landscape of existing research on drug resistance prevalence for dolutegravir and possible evolutionary explanations on how these mutations arise in the first place, leading to implications in developing more robust treatment modalities.
检查现状:用于艾滋病治疗的多替拉韦的进化解释和耐药性流行情况(综述)
自 20 世纪 80 年代初发现艾滋病病毒以来,艾滋病药物治疗取得了长足的进步。整合酶链转移抑制剂(INSTIs)是目前用于治疗艾滋病的七种药物之一,可使艾滋病病毒感染者(PLWH)的血样中检测不到病毒数量。据记载,第一代 INSTIs 的基因耐药障碍较低,这表明导致耐药突变的突变数量较少。第二代 INSTI 多鲁曲韦的问世显示出更高的遗传抗性屏障,这将减少 INSTIs 的耐药突变,并提高该类艾滋病治疗的整体有效性。艾滋病毒感染者可根据他们以前/现在是否接受过治疗或从未接受过治疗进行分类。与对多鲁曲韦的实际耐药性相比,治疗新手和既往接受过治疗(成功或失败)的艾滋病患者报告的耐药突变率不同,分别为 0.4-31% 和 0.1-67.2%。基因耐药性的进化因素(包括表观相互作用和点突变)表明,这些耐药突变既有非多态突变,也有多态突变。对进化因素如何导致艾滋病毒耐药性的不完全了解凸显了开展进一步研究的重要性。这项研究可能有助于提高第二代 INSTIs 在 PLWH 未来治疗方案中的疗效。本综述介绍了现有的多罗替拉韦耐药率研究概况,以及这些变异如何首先产生的可能的进化解释,从而对开发更强大的治疗模式产生影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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