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.

Q2 Pharmacology, Toxicology and Pharmaceutics Antiviral Chemistry and Chemotherapy Pub Date : 2021-01-01 DOI:10.1177/20402066211030380
M E Lewis, P Simpson, J Mori, B Jubb, J Sullivan, L McFadyen, E van der Ryst, C Craig, D L Robertson, M Westby
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Abstract

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.Clinical trial registration numbers (ClinicalTrials.gov): NCT00098306 and NCT00098722.

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在接受优化背景方案的hiv -1感染者中,V3-Loop基因型不能预测嗜ccr5病毒的马拉韦洛克易感性或48周后的临床反应。
在第24周的MOTIVATE研究中,35名接受马拉韦洛克治疗的病毒学失败参与者中有15名的病毒和嗜ccr5 (R5)病毒降低了马拉韦洛克的敏感性。处理后,在病毒包膜糖蛋白120第三变量(V3)环茎和尖端观察到氨基酸的变化,并且在病毒之间有所不同。没有氨基酸的变化可以可靠地预测易感性的降低,这表明抗性是遗传环境依赖的。到第24周,依从性差与马拉韦洛克易感病毒学失败相关,而马拉韦洛克易感性降低与背景方案活性次优相关,强调了整体方案活性和良好依从性的重要性。回顾性评估了48周病毒学失败参与者的预处理病毒中含有这些第24周突变或其他变体的预处理v3环序列的预测值,这些变体存在于>3%的预处理病毒中。第48周的临床结果评估了704名参与者的预处理v3环ccr5序列(366名应答者;338例病毒学失败[83例R5病毒伴马拉韦洛克敏感性评估]。在23个v3环残基中鉴定出75个流行率>3%的氨基酸变异。先前确定的与单个分离株耐药相关的变异有代表性,但没有一个与单独或联合病毒学失败可靠相关。单因素分析显示变异4L、11R和19S (P)与病毒学失败相关。临床试验注册号(ClinicalTrials.gov): NCT00098306和NCT00098722。
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来源期刊
Antiviral Chemistry and Chemotherapy
Antiviral Chemistry and Chemotherapy Pharmacology, Toxicology and Pharmaceutics-Pharmacology
CiteScore
5.20
自引率
0.00%
发文量
5
审稿时长
15 weeks
期刊介绍: Antiviral Chemistry & Chemotherapy publishes the results of original research concerned with the biochemistry, mode of action, chemistry, pharmacology and virology of antiviral compounds. Manuscripts dealing with molecular biology, animal models and vaccines are welcome. The journal also publishes reviews, pointers, short communications and correspondence.
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