Emory Vaccine Center and Yerkes National Primate Research Center, Emory University, Atlanta, GA, USA.
J Virol. 2013 Jan;87(2):708-15. doi: 10.1128/JVI.02118-12. Epub 2012 Oct 31.
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.
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。