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程序性死亡受体1(PD-1)上调与典型进展者中HIV特异性记忆性CD8 + T细胞耗竭相关,但在长期不进展者中并非如此。

PD-1 up-regulation is correlated with HIV-specific memory CD8+ T-cell exhaustion in typical progressors but not in long-term nonprogressors.

作者信息

Zhang Ji-Yuan, Zhang Zheng, Wang Xicheng, Fu Jun-Liang, Yao Jinxia, Jiao Yanmei, Chen Liangen, Zhang Hui, Wei Jianan, Jin Lei, Shi Ming, Gao George Fu, Wu Hao, Wang Fu-Sheng

机构信息

Institute of Microbiology, Chinese Academy of Sciences, Beijing, China.

出版信息

Blood. 2007 Jun 1;109(11):4671-8. doi: 10.1182/blood-2006-09-044826. Epub 2007 Feb 1.

Abstract

The immunoreceptor PD-1 is significantly up-regulated on exhausted CD8+ T cells during chronic viral infections such as HIV-1. However, it remains unknown whether PD-1 expression on CD8+ T cells differs between typical progressors (TPs) and long-term nonprogressors (LTNPs). In this report, we examined PD-1 expression on HIV-specific CD8+ T cells from 63 adults with chronic HIV infection. We found that LTNPs exhibited functional HIV-specific memory CD8+ T cells with markedly lower PD-1 expression. TPs, in contrast, showed significantly up-regulated PD-1 expression that was closely correlated with a reduction in CD4 T-cell number and an elevation in plasma viral load. Importantly, PD-1 up-regulation was also associated with reduced perforin and IFN-gamma production, as well as decreased HIV-specific effector memory CD8+ T-cell proliferation in TPs but not LTNPs. Blocking PD-1/PD-L1 interactions efficiently restored HIV-specific CD8+ T-cell effector function and proliferation. Taken together, these findings confirm the hypothesis that high PD-1 up-regulation mediates HIV-specific CD8+ T-cell exhaustion. Blocking the PD-1/PD-L1 pathway may represent a new therapeutic option for this disease and provide more insight into immune pathogenesis in LTNPs.

摘要

免疫受体PD-1在慢性病毒感染(如HIV-1)期间,在耗竭的CD8+ T细胞上显著上调。然而,典型进展者(TPs)和长期不进展者(LTNPs)的CD8+ T细胞上PD-1的表达是否存在差异仍不清楚。在本报告中,我们检测了63例慢性HIV感染成人的HIV特异性CD8+ T细胞上的PD-1表达。我们发现,LTNPs表现出功能性HIV特异性记忆CD8+ T细胞,其PD-1表达明显较低。相比之下,TPs的PD-1表达显著上调,这与CD4 T细胞数量减少和血浆病毒载量升高密切相关。重要的是,PD-1上调还与穿孔素和干扰素-γ产生减少以及HIV特异性效应记忆CD8+ T细胞增殖减少有关,TPs中如此,但LTNPs中并非如此。阻断PD-1/PD-L1相互作用可有效恢复HIV特异性CD8+ T细胞效应功能和增殖。综上所述,这些发现证实了高PD-1上调介导HIV特异性CD8+ T细胞耗竭的假说。阻断PD-1/PD-L1途径可能代表了针对该疾病的一种新的治疗选择,并为LTNPs的免疫发病机制提供了更多见解。

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