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Evolution of Envelope Sequences of Human Immunodeficiency Virus Type 1 in Cellular Reservoirs in the Setting of Potent Antiviral Therapy

机译:在有效的抗病毒治疗的背景下人类免疫缺陷病毒1型信封序列在细胞水库中的演变。

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摘要

In human immunodeficiency virus (HIV)-infected patients treated with potent antiretroviral therapy, the persistence of latently infected cells may reflect the long decay half-life of this cellular reservoir or ongoing viral replication at low levels with continuous replenishment of the population or both. To address these possibilities, sequences encompassing the C2 and V3 domains of HIV-1 env were analyzed from virus present in baseline plasma and from viral isolates obtained after 2 years of suppressive therapy in six patients. The presence of sequence changes consistent with evolution was demonstrated for three subjects and correlated with less complete suppression of viral replication, as indicated by the rapidity of the initial virus load decline or the intermittent reappearance of even low levels of detectable viremia. Together, these results provide evidence for ongoing replication. In the remaining three patients, virus recovered after 2 years of therapy was either genotypically contemporary with or ancestral to virus present in plasma 2 years before, indicating that virus recovery had indeed resulted from activation of latently infected cells.
机译:在接受有效抗逆转录病毒疗法治疗的人类免疫缺陷病毒(HIV)感染的患者中,潜伏感染细胞的持续存在可能反映了该细胞库的长衰变半衰期或低水平的病毒复制,并伴随着种群的不断补充。为了解决这些可能性,从基线血浆中存在的病毒以及经过抑制治疗2年后获得的病毒分离株中分析了HIV-1 env C2和V3结构域的序列,对6名患者进行了分析。对于三个对象,证实了与进化相一致的序列变化的存在,并且与病毒复制的较不完全抑制相关,如初始病毒载量下降的速度或即使低水平的可检测病毒血症的间歇性重新出现所表明的。这些结果共同为正在进行的复制提供了证据。在剩下的三名患者中,治疗2年后恢复的病毒在基因型上与2年以前血浆中存在的病毒相近,或者是祖先存在于血浆中,这表明病毒的恢复确实是由潜伏感染细胞的激活引起的。

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