Kim Nayoung, Dabrowska Alicja, Jenner Richard G, Aldovini Anna
Children's Hospital Boston, Department of Medicine, Harvard Medical School, Boston, Massachusetts 02115, USA.
J Virol. 2007 Jul;81(14):7584-97. doi: 10.1128/JVI.02616-06. Epub 2007 May 9.
Human immunodeficiency virus (HIV) and simian immunodeficiency virus (SIV) infections lead to AIDS in humans and rhesus macaques (RM), while they are asymptomatic in species naturally infected with SIV, such as chimpanzees, sooty mangabeys (SM), and African green monkeys (AGM). Differential CD4(+) T-cell apoptosis may be responsible for these species-specific differences in susceptibility to disease. To identify factors that influence the different apoptotic responses of these species, we analyzed virus-infected human and nonhuman primate peripheral blood mononuclear cells (PBMC). We found that the apoptotic factor TRAIL was present at higher levels in human and RM PBMC cultures and was mediating, at least in part, CD4(+) T-cell apoptosis in these cultures. The species-specific increase in TRAIL and death receptor expression observed with cultures also occurred in vivo in SIV-infected RM but not in SIV-infected SM. In human and RM myeloid immature dendritic cells and macrophages, the virus-induced expression of TRAIL and other interferon-inducible genes, which did not occur in the same cells from chimpanzee, SM, and AGM, was Tat dependent. Our results link the differential induction of TRAIL in human and nonhuman primate cells to species-specific differences in disease susceptibility.
人类免疫缺陷病毒(HIV)和猿猴免疫缺陷病毒(SIV)感染分别导致人类和恒河猴(RM)患上艾滋病,而在自然感染SIV的物种(如黑猩猩、乌黑白眉猴(SM)和非洲绿猴(AGM))中,它们却不会引发症状。不同的CD4(+) T细胞凋亡可能是造成这些物种对疾病易感性存在差异的原因。为了确定影响这些物种不同凋亡反应的因素,我们分析了病毒感染的人类和非人灵长类动物外周血单核细胞(PBMC)。我们发现,凋亡因子TRAIL在人类和恒河猴PBMC培养物中的水平较高,并且至少在一定程度上介导了这些培养物中CD4(+) T细胞的凋亡。在培养物中观察到的TRAIL和死亡受体表达的物种特异性增加,在体内感染SIV的恒河猴中也出现了,但在感染SIV的乌黑白眉猴中却没有。在人类和恒河猴的髓系未成熟树突状细胞和巨噬细胞中,病毒诱导的TRAIL和其他干扰素诱导基因的表达是Tat依赖性的,而在黑猩猩、乌黑白眉猴和非洲绿猴的相同细胞中则不会发生这种情况。我们的结果将人类和非人灵长类动物细胞中TRAIL的差异诱导与疾病易感性的物种特异性差异联系了起来。