Suppressor CD8+ T cells in HIV infection

描述(申请人提供)：描述了CD8T抑制淋巴细胞。然而，IL-10CD8ts在调节HIV特异性T细胞反应中的调节作用仍不清楚。这项研究计划中提出的目标包括一系列实验，旨在探索HIV特异性IL-10 CD8 T细胞在介导HIV感染中T细胞免疫功能障碍中的作用。我假设HIV特异性IL-10 CD8 T细胞对不同人群的HIV特异性效应T细胞有抑制作用。目的1探讨IL-10 CD8转录因子在HIV感染过程中的抑制作用机制。1)接触依赖抑制，2)细胞因子，如IL-10和转化生长因子-β，将被研究。目的2研究人类免疫缺陷病毒(HIV)感染过程中IL-10CD8ts的表型特征和特异性。这一目标将集中于检测IL-10CD8ts对不同HIV和非HIV特异性效应T细胞的抑制作用。还将评估与调节性T细胞相关的各种标志物，如CD25、FoxpS、CTLA-4的IL-10 CD8表达。

DESCRIPTION (provided by applicant): CD8+ T suppressor lymphocytes have been described. However, the regulatory role of IL-10+ CD8+ Ts in modulating HIV-specific T cell responses remains unknown. The aims proposed in this research plan contain a series of experiments designed to explore the role of HIV-specific IL-10+ CD8+ T cells in mediating T cell immune dysfunction in HIV infection. I hypothesize that HIV-specific IL-10+ CD8+ T cells exert an inhibitory effect on distinct populations of HIV-specific effector T cells. Aim 1 explores the mechanisms of suppression utilized by the IL-10+ CD8+ Ts during HIV infection. The role of 1) contact dependent suppression, 2) cytokines such as IL-10 and TGF-beta, will be examined. Aim 2 investigates the phenotypic characteristics and specificity of the IL-10+ CD8+ Ts during HIV infection. This aim will focus on examining the suppressive effect of the IL-10+ CD8+ Ts to different HIV, and non-HIV-specific effector T cells. The expression by the IL- 10+ CD8+ Ts of various markers associated with regulatory T cells, such as CD25, FoxpS, CTLA-4 will also be assessed.