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Immunology Mechanism of CD4+ CD25 T Regulatory Cells Acting on Effector T Cells

机译:CD4 + CD25 T调节细胞作用于效应T细胞的免疫学机制

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Objective: To detect the inhibiting co-stimulating molecule CTLA4 and cytokines secreted by Treg cells, and explore the immunology mechanism of T regulatory cells acting on effector T cells in co-cultured system(CCS) and separating-cultured system(SCS). Methods: Detecting the percentage of CTLA4 and CD28 expressed on the Treg ceils and effector T ceils, and then adding Treg cells to mixed lymphocyte reaction(MLR) system in CCS and TransWeil Milliceil-PCF SCS, at the same time, adding or not adding anti-IL-10 or anti-TGF.II1 to the reacting systems, examining the inhibitory capacity of Treg ceils exerting on the MLR. Results: Compared with effector T cells, Treg cells expressed higher level CTLA4 and secreted much more IL-10 and TGF-β(P<0.01). The inhibitory capacity of Treg cells co-cultured with effector T ceils is much stronger than that in separating cultured group(P<0.01). Moreover, the inhibiting rate of Treg ceils exerting on effector T ceils through secretin_g IL-10 was more powerful than that through secreting TGF-β1 (P<0.01). Coaclusion: Both ceil-to-ceil contact and cytokines secretion mechanisms are involved in CD4+ CD25+ Treg ceils operating function. However, the former is more important. Intresfingly, we for the first time pointfound that IL-10 plays more powerful roles than TGF-β1 in the cytokines secretion mechanism.
机译:目的:检测共培养系统(CCS)和分离培养系统(SCS)中Treg细胞分泌的抑制性共刺激分子CTLA4和细胞因子,探讨T调节细胞作用于效应T细胞的免疫学机制。方法:检测Treg细胞和效应T细胞中CTLA4和CD28表达的百分比,然后在CCS和TransWeil Milliceil-PCF SCS中的混合淋巴细胞反应(MLR)系统中添加Treg细胞,同时添加或不添加抗IL-10或抗TGF.II1到反应系统,检查Treg细胞对MLR的抑制能力。结果:与效应T细胞相比,Treg细胞表达更高水平的CTLA4,并分泌更多的IL-10和TGF-β(P <0.01)。与效应T细胞共培养的Treg细胞抑制能力强于分离培养组(P <0.01)。此外,通过分泌蛋白-g IL-10对Treg细胞施加于效应T细胞的抑制作用比通过分泌TGF-β1的抑制作用更强(P <0.01)。共存:细胞与细胞的接触和细胞因子的分泌机制均参与CD4 + CD25 + Treg细胞的运行功能。但是,前者更为重要。有趣的是,我们首次发现IL-10在细胞因子分泌机制中比TGF-β1发挥更强大的作用。

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