首页> 美国卫生研究院文献>AIDS Research and Human Retroviruses >Female Genital Tract Shedding of CXCR4-Tropic HIV Type 1 Is Associated with a Majority Population of CXCR4-Tropic HIV Type 1 in Blood and Declining CD4+ Cell Counts
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Female Genital Tract Shedding of CXCR4-Tropic HIV Type 1 Is Associated with a Majority Population of CXCR4-Tropic HIV Type 1 in Blood and Declining CD4+ Cell Counts

机译:CXCR4热带艾滋病毒1型女性生殖道脱落与血液中CXCR4热带艾滋病毒1型多数人群和CD4 +细胞计数下降有关

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摘要

This study compared HIV-1 genotypes shed over time (≤3.5 years) in the vaginal secretions (VS) and blood plasma (BP) of 15 chronically infected women. Analysis of predicted coreceptor tropism (CCR5 = R5, CXCR4 = X4) for quasispecies shedding revealed three patterns: (1) viral quasispecies shed in both VS and BP were restricted to R5-tropism at all time points, (2) quasispecies shed in VS were restricted to R5-tropism at all time points but X4 quasispecies were identified in the BP at one or more time points, and (3) quasispecies shed in matched VS and BP both contained X4-tropic viruses. Overall, the frequency of X4 quasispecies circulation in VS was 2-fold less than in BP and detection of X4 virus in VS was more likely to occur when X4 quasispecies comprised more than 50% of BP viruses (p = 0.01) and when declines in blood CD4+ lymphocyte levels were the greatest (p = 0.038). Additionally, the mean number of predicted N-glycosylation sites between matched VS and BP samples was strongly correlated (r = 0.86, p< 0.0001) with glycosylation densities in the following order (VS R5 = BP R5 > BP X4 > VS X4). The X4 glycosylation densities may result from compartmentalization pressures in the female genital tract or the delayed appearance of these viruses in VS. Our results suggest that the presence of X4 virus in VS is associated with a threshold population of X4 quasispecies in BP, which are increasing during the HIV-induced failure of the human immune system.
机译:这项研究比较了15位慢性感染妇女的阴道分泌物(VS)和血浆(BP)随时间流逝(≤3.5年)的HIV-1基因型。对准种脱落的预测共受体向性(CCR5 = R5,CXCR4 = X4)的分析揭示了三种模式:(1)在VS和BP中均发生病毒准种在所有时间点均受限于R5-向性,(2)在VS中脱落的准种在所有时间点都被限制为R5-向性,但在一个或多个时间点在BP中鉴定出X4准种,并且(3)在匹配的VS和BP中脱落的准种都包含X4向性病毒。总体而言,VS中X4准种的循环频率比BP少2倍,并且当X4准种占BP病毒的50%以上(p = 0.01)并且当NP下降时,更可能在VS中检测到X4病毒。血液中CD4 + 淋巴细胞水平最高(p = 0.038)。此外,匹配的VS和BP样品之间的预测N-糖基化位点的平均数量与糖基化密度的相关性极强(r = 0.86,p <0.0001)(VS R5 = BP R5> BP X4> VS X4)。 X4糖基化密度可能是由于女性生殖道内的分隔压力或这些病毒在VS中出现延迟所致。我们的结果表明,VS中X4病毒的存在与BP中X4准种的阈值种群有关,该阈值种群在HIV诱导的人类免疫系统衰竭期间不断增加。

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