CD160和2B4的高表达定义了精英控制者中具有细胞溶解作用的HIV特异性CD8 + T细胞群体。
Elevated Expression of CD160 and 2B4 Defines a Cytolytic HIV-Specific CD8+ T-Cell Population in Elite Controllers.
作者信息
Pombo Carolina, Wherry E John, Gostick Emma, Price David A, Betts Michael R
机构信息
Department of Microbiology, Perelman School of Medicine, University of Pennsylvania, Philadelphia.
Department of Microbiology, Perelman School of Medicine, University of Pennsylvania, Philadelphia Institute for Immunology, Perelman School of Medicine, University of Pennsylvania, Philadelphia.
出版信息
J Infect Dis. 2015 Nov 1;212(9):1376-86. doi: 10.1093/infdis/jiv226. Epub 2015 Apr 15.
During chronic human immunodeficiency virus (HIV) infection, virus-specific CD8(+) T cells become functionally exhausted. Unlike most chronically infected individuals, elite controllers of HIV retain CD8(+) T-cell polyfunctionality and cytolytic capacity. It remains unclear whether elite controllers manifest T-cell exhaustion similar to subjects with chronic progression of HIV infection. Here we assessed coexpression of PD-1, Lag-3, CD160, and 2B4 as a measure of T-cell exhaustion in a cohort of elite controllers and in chronic progressors. We found that elite controllers have a high proportion of potentially exhausted (PD1(+)CD160(+)2B4(+)) HIV-specific CD8(+) T cells that is comparable to the proportion in chronic progressors. However, elite controllers also harbor a population of HIV-specific CD160(+)2B4(+) CD8(+) T cells that correlates with cytolytic capacity, as measured by perforin expression, a population not commonly present in chronic progressors. We therefore propose that coexpression of CD160 and 2B4 delineates a population of cytolytic CD8(+) T cells important for the control of HIV.
在人类免疫缺陷病毒(HIV)慢性感染期间,病毒特异性CD8(+) T细胞功能耗竭。与大多数慢性感染个体不同,HIV精英控制者保留了CD8(+) T细胞的多功能性和细胞溶解能力。目前尚不清楚精英控制者是否表现出与HIV感染慢性进展患者类似的T细胞耗竭。在此,我们评估了精英控制者队列和慢性进展者队列中PD-1、Lag-3、CD160和2B4的共表达情况,以此作为T细胞耗竭的指标。我们发现,精英控制者中潜在耗竭(PD1(+)CD160(+)2B4(+))的HIV特异性CD8(+) T细胞比例很高,与慢性进展者中的比例相当。然而,精英控制者还存在一群HIV特异性CD160(+)2B4(+) CD8(+) T细胞,其与通过穿孔素表达衡量的细胞溶解能力相关,而慢性进展者中通常不存在这类细胞。因此,我们提出CD160和2B4的共表达界定了一群对控制HIV很重要的细胞溶解CD8(+) T细胞。