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

被引:239
作者
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 [1 ]
机构
[1] Beijing 302 Hosp, Res Ctr Biol Therapy, Beijing 100039, Peoples R China
[2] Chinese Acad Sci, Inst Microbiol, Beijing, Peoples R China
[3] Capital Univ Med Sci, Beijing You an Hosp, Dept Infect Dis, Beijing, Peoples R China
[4] Beijing Guang An Med Hosp, HIV AIDS Res Ctr, Beijing, Peoples R China
关键词
D O I
10.1182/blood-2006-09-044826
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
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.
引用
收藏
页码:4671 / 4678
页数:8
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