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

Ji‐Yuan Zhang(Chinese Academy of Sciences), Zheng Zhang(302 Military Hospital of China), Xicheng Wang(Beijing YouAn Hospital), Junliang Fu(302 Military Hospital of China), Jinxia Yao(302 Military Hospital of China), Yanmei Jiao(Beijing YouAn Hospital), Liangen Chen(302 Military Hospital of China), Hui Zhang(302 Military Hospital of China), Jianan Wei, Lei Jin(302 Military Hospital of China), Ming Shi(302 Military Hospital of China), George F. Gao(Chinese Academy of Sciences), Hao Wu(Beijing YouAn Hospital), Fu‐Sheng Wang(Chinese Academy of Sciences)
Blood
February 3, 2007
Cited by 294Open Access
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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.


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