Presence of suppressor HIV-specific CD8+ T cells is associated with increased PD-1 expression on effector CD8+ T cells

被引:31
|
作者
Elrefaei, Mohamed [1 ]
Baker, Chris A. R.
Jones, Norman G.
Bangsberg, David R. [2 ]
Cao, Huyen
机构
[1] Calif Dept Publ Hlth, VRDL, Richmond, CA 94804 USA
[2] Univ Calif San Francisco, Dept Med, San Francisco, CA 94143 USA
来源
JOURNAL OF IMMUNOLOGY | 2008年 / 180卷 / 11期
关键词
D O I
10.4049/jimmunol.180.11.7757
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Mechanisms leading to the observed immune dysregulation in HIV-1 infection are not well understood. HIV-specific IL-10-positive CD8(+) T cells are increased in advanced HIV disease. We have previously reported that Gag-specific IL-10-positive CD8(+) T cells suppressed cytolysis. In this study we describe the suppressive effect of Nef-specific IL-10-positive CD8(+) T cells. Interestingly, simultaneous removal of both Gag- and Nef-specific IL-10-positive CD8(+) T cells led to higher HIV-specific cytolysis compared with the removal of Nef-specific IL-10-positive CD8(+) T cells alone. We also examined the level of programmed cell death-1 (PD-1) as a measure of immune dysfunction in association with IL-10-positive suppressor CD8(+) T cells. The level of PD-1 expression on CD107-positive effector CD8(+) T cells was significantly increased when IL-10-positive suppressor CD8(+) T cells were present (P < 0.05). Our results suggest that IL-10-positive suppressor CD8(+) T cells contribute to the immune dysfunction observed in advanced HIV infection and that the concomitant presence of multiple IL-10-positive CD8(+) T cell populations may have an additive suppressive effect.
引用
收藏
页码:7757 / 7763
页数:7
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