首页> 美国卫生研究院文献>PLoS Pathogens >Lack of Detectable HIV-1 Molecular Evolution during Suppressive Antiretroviral Therapy
【2h】

Lack of Detectable HIV-1 Molecular Evolution during Suppressive Antiretroviral Therapy

机译:抑制抗逆转录病毒疗法过程中缺乏可检测的HIV-1分子进化。

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

A better understanding of changes in HIV-1 population genetics with combination antiretroviral therapy (cART) is critical for designing eradication strategies. We therefore analyzed HIV-1 genetic variation and divergence in patients' plasma before cART, during suppression on cART, and after viral rebound. Single-genome sequences of plasma HIV-1 RNA were obtained from HIV-1 infected patients prior to cART (N = 14), during suppression on cART (N = 14) and/or after viral rebound following interruption of cART (N = 5). Intra-patient population diversity was measured by average pairwise difference (APD). Population structure was assessed by phylogenetic analyses and a test for panmixia. Measurements of intra-population diversity revealed no significant loss of overall genetic variation in patients treated for up to 15 years with cART. A test for panmixia, however, showed significant changes in population structure in 2/10 patients after short-term cART (<1 year) and in 7/10 patients after long-term cART (1–15 years). The changes consisted of diverse sets of viral variants prior to cART shifting to populations containing one or more genetically uniform subpopulations during cART. Despite these significant changes in population structure, rebound virus after long-term cART had little divergence from pretherapy virus, implicating long-lived cells infected before cART as the source for rebound virus. The appearance of genetically uniform virus populations and the lack of divergence after prolonged cART and cART interruption provide strong evidence that HIV-1 persists in long-lived cells infected before cART was initiated, that some of these infected cells may be capable of proliferation, and that on-going cycles of viral replication are not evident.
机译:结合抗逆转录病毒疗法(cART)更好地了解HIV-1人群遗传学的变化对于设计根除策略至关重要。因此,我们分析了cART之前,cART抑制期间以及病毒反弹后患者血浆中HIV-1的遗传变异和差异。血浆HIV-1 RNA的单基因组序列是在cART之前(N = 14),cART抑制期间(N = 14)和/或cART中断后病毒反弹后(N = 5)从HIV-1感染患者获得的。 )。通过平均成对差异(APD)测量患者的人群多样性。人口结构通过系统发育分析和泛滥症测试进行评估。种群内多样性的测量结果显示,使用cART治疗长达15年的患者的总体遗传变异没有明显的损失。但是,一项对全棉混合症的测试显示,短期cART(<1年)后2/10例患者和长期cART(1-15年)后7/10例患者的人群结构发生了显着变化。这些变化包括在cART之前转移到包含一个或多个遗传上均一的亚群的种群之前,cART之前的各种病毒变体集。尽管种群结构发生了显着变化,但长期cART后的反弹病毒与治疗前病毒几乎没有差异,这意味着cART之前感染的长寿细胞是反弹病毒的来源。遗传上均一的病毒种群的出现以及长时间的cART和cART中断后缺乏差异性提供了有力的证据,表明在cART启动之前被感染的长寿细胞中HIV-1仍然存在,其中一些被感染的细胞可能具有增殖能力,并且病毒复制的持续周期尚不明显。

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号