首页> 美国卫生研究院文献>Antiviral Chemistry Chemotherapy >V3-Loop genotypes do not predict maraviroc susceptibility of CCR5-tropic virus or clinical response through week 48 in HIV-1–infected treatment-experienced persons receiving optimized background regimens
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V3-Loop genotypes do not predict maraviroc susceptibility of CCR5-tropic virus or clinical response through week 48 in HIV-1–infected treatment-experienced persons receiving optimized background regimens

机译:V3循环基因型不会通过HIV-1感染治疗经验丰富的人员在接受优化的背景方案中通过第48周预测CCR5-热带病毒或临床反应的马拉维毒易感性

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摘要

Viruses from 15 of 35 maraviroc-treated participants with virologic failure and CCR5-tropic (R5) virus in the MOTIVATE studies at Week 24 had reduced maraviroc susceptibility. On-treatment amino acid changes were observed in the viral envelope glycoprotein 120 third variable (V3)–loop stems and tips and differed between viruses. No amino acid change reliably predicted reduced susceptibility, indicating that resistance was genetic context–dependent. Through Week 24, poor adherence was associated with maraviroc-susceptible virologic failure, whereas reduced maraviroc susceptibility was associated with suboptimal background regimen activity, highlighting the importance of overall regimen activity and good adherence. Predictive values of pretreatment V3-loop sequences containing these Week 24 mutations or other variants present at >3% in pretreatment viruses of participants with virologic failure at Week 48 were retrospectively assessed. Week 48 clinical outcomes were evaluated for correlates with pretreatment V3-loop CCR5-tropic sequences from 704 participants (366 responders; 338 virologic failures [83 with R5 virus with maraviroc susceptibility assessment]). Seventy-five amino acid variants with >3% prevalence were identified among 23 V3-loop residues. Previously identified variants associated with resistance in individual isolates were represented, but none were associated reliably with virologic failure alone or in combination. Univariate analysis showed virologic-failure associations with variants 4L, 11R, and 19S (P < 0.05). However, 11R is a marker for CXCR4 tropism, whereas neither 4L nor 19S was reliably associated with reduced maraviroc susceptibility in R5 failure. These findings from a large study of V3-loop sequences confirm lack of correlation between V3-loop genotype and clinical outcome in participants treated with maraviroc.
机译:在第24周的第24周的病毒衰竭和CCR5-热带(R5)病毒中的15个具有病毒学衰竭和CCR5-Tropic(R5)病毒的病毒减少了Maraviroc易感性。在病毒包膜糖蛋白120第三变量(V3)中观察到在治疗氨基酸变化 - 茎和尖端,不同于病毒。没有氨基酸变化可靠地预测降低易感性,表明阻力是遗传上下文依赖性。通过第24周,粘附不良与易受玛拉维病毒的病毒学衰竭有关,而降低的马拉西病易感性与次优背景中的活动相关,突出了整体方案活动的重要性和良好的依从性。回顾性评估了在第48周,在第48周,在第48周的参与者预处理病毒失败的预处理V3环序列的预测值V3环序列或存在于参与者的预处理病毒的预处理病毒。每周48个临床结果评估来自704名参与者的预处理V3环CCR5-热带序列的相关性(366名响应者; 338个病毒学失败[83带有Maraviroc易感性评估的R5病毒])。在23V3环残基中鉴定了具有> 3%患病率的七十五氨基酸变体。以前鉴定了与个体分离株的抗性相关的变体,但没有与种质失败单独或组合可靠地相关。单变量分析显示与变体4L,11R和19S的病毒学破坏关联(P <0.05)。然而,11r是CXCR4覆身的标志物,而4L也没有19s与R5衰竭的降低的Maraviroc易感性无能为力地相关。来自V3环序列的大型研究的这些发现证实了用马拉西瓦治疗的参与者的V3环基因型和临床结果之间缺乏相关性。

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