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Role of transmitted Gag CTL polymorphisms in defining replicative capacity and early HIV-1 pathogenesis.传播性 Gag CTL 多态性在定义复制能力和早期 HIV-1 发病机制中的作用。
PLoS Pathog. 2012;8(11):e1003041. doi: 10.1371/journal.ppat.1003041. Epub 2012 Nov 29.
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HIV-1 dynamics: a reappraisal of host and viral factors, as well as methodological issues.HIV-1 动力学:宿主和病毒因素以及方法学问题的再评价。
Viruses. 2012 Oct 10;4(10):2080-96. doi: 10.3390/v4102080.
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Is the virulence of HIV changing? A meta-analysis of trends in prognostic markers of HIV disease progression and transmission.HIV 的毒力是否在发生变化?一项关于 HIV 疾病进展和传播的预后标志物趋势的荟萃分析。
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Role of donor genital tract HIV-1 diversity in the transmission bottleneck.供体生殖道 HIV-1 多样性在传播瓶颈中的作用。
Proc Natl Acad Sci U S A. 2011 Nov 15;108(46):E1156-63. doi: 10.1073/pnas.1103764108. Epub 2011 Nov 7.
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HLA-A*7401-mediated control of HIV viremia is independent of its linkage disequilibrium with HLA-B*5703.HLA-A*7401 对 HIV 病毒血症的控制与其与 HLA-B*5703 的连锁不平衡无关。
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Influence of Gag-protease-mediated replication capacity on disease progression in individuals recently infected with HIV-1 subtype C. gag 蛋白酶介导的复制能力对近期感染 HIV-1 亚型 C 的个体疾病进展的影响。
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The influence of human leukocyte antigen class I alleles and their population frequencies on human immunodeficiency virus type 1 control among African Americans.人类白细胞抗原 I 类等位基因及其群体频率对非裔美国人中人类免疫缺陷病毒 1 型控制的影响。
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The major genetic determinants of HIV-1 control affect HLA class I peptide presentation.HIV-1 控制的主要遗传决定因素影响 HLA Ⅰ类肽的呈递。
Science. 2010 Dec 10;330(6010):1551-7. doi: 10.1126/science.1195271. Epub 2010 Nov 4.
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Phylogenetic approach reveals that virus genotype largely determines HIV set-point viral load.系统进化方法揭示病毒基因型在很大程度上决定了 HIV 病毒载量的基准值。
PLoS Pathog. 2010 Sep 30;6(9):e1001123. doi: 10.1371/journal.ppat.1001123.
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T cell immunity in acute HIV-1 infection.急性 HIV-1 感染中的 T 细胞免疫。
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宿主和病毒因素对早期感染期间 HIV-1 病毒载量控制的累积影响。

Cumulative impact of host and viral factors on HIV-1 viral-load control during early infection.

机构信息

Emory Vaccine Center and Yerkes National Primate Research Center, Emory University, Atlanta, GA, USA.

出版信息

J Virol. 2013 Jan;87(2):708-15. doi: 10.1128/JVI.02118-12. Epub 2012 Oct 31.

DOI:10.1128/JVI.02118-12
PMID:23115285
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3554094/
Abstract

In HIV-1 infection, the early set-point viral load strongly predicts both viral transmission and disease progression. The factors responsible for the wide spectrum of set-point viral loads are complex and likely reflect an interplay between the transmitted virus and genetically defined factors in both the transmitting source partner and the seroconverter. Indeed, analysis of 195 transmission pairs from Lusaka, Zambia, revealed that the viral loads in transmitting source partners contributed only ∼2% of the variance in early set-point viral loads of seroconverters (P = 0.046 by univariable analysis). In multivariable models, early set-point viral loads in seroconverting partners were a complex function of (i) the viral load in the source partner, (ii) the gender of the seroconverter, (iii) specific HLA class I alleles in the newly infected partner, and (iv) sharing of HLA-I alleles between partners in a transmission pair. Each of these factors significantly and independently contributed to the set-point viral load in the newly infected partner, accounting for up to 37% of the variance observed and suggesting that many factors operate in concert to define the early virological phenotype in HIV-1 infection.

摘要

在 HIV-1 感染中,早期设定点病毒载量强烈预测病毒传播和疾病进展。导致设定点病毒载量广泛谱的因素很复杂,可能反映了传播病毒与传播源伴侣和血清转化者中遗传定义因素之间的相互作用。事实上,对来自赞比亚卢萨卡的 195 对传播对的分析表明,传播源伴侣中的病毒载量仅对血清转化者早期设定点病毒载量的变异贡献了约 2%(单变量分析 P = 0.046)。在多变量模型中,血清转化者的早期设定点病毒载量是源伴侣病毒载量、(ii)血清转化者的性别、(iii)新感染伴侣中特定 HLA Ⅰ类等位基因以及(iv)传播对中伴侣之间 HLA-I 等位基因共享的复杂函数。这些因素都显著且独立地促成了新感染伴侣的设定点病毒载量,占观察到的变异的高达 37%,表明许多因素协同作用来定义 HIV-1 感染中的早期病毒学表型。