T细胞亚群的分化和功能。

T R Mosmann, L Li, H Hengartner, D Kagi, W Fu, S Sad
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引用次数: 61

摘要

CD8+ T效应细胞的Tc1和Tc2亚群分泌不同模式的细胞因子,但具有相似的功能,包括穿孔素和fas依赖的细胞毒性,以及诱导迟发性超敏反应(DTH),包括水肿和粒细胞浸润。Tc1 (γ -干扰素)和Tc2(白细胞介素4和5)的特征性细胞因子在DTH反应中在体内表达。缺乏细胞因子合成的Tc1细胞也会诱导相似水平的DTH,支持CD8+ T细胞细胞因子模式与DTH之间缺乏相关性。CD8+ T细胞通常比CD4细胞产生更低的细胞因子水平,因为CD8细胞在完全刺激发生之前杀死了它们的抗原呈递细胞。这种影响可以通过增加刺激频率或使用穿孔素缺陷T细胞来抵消。基于正常免疫反应涉及复杂的细胞因子混合物的原理,细胞因子对CD8+ T细胞分化的多参数分析已经开始。检测7种细胞因子的所有组合。在某些组合中,不能从单个细胞因子的功能来预测联合效应。在这种情况下,白细胞介素4、10和12可能对CD8+ T细胞分化产生相反的影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Differentiation and functions of T cell subsets.

The Tc1 and Tc2 subsets of CD8+ T effector cells secrete different patterns of cytokines, but have similar functions, including perforin- and Fas-dependent cytotoxicity, and induction of delayed type hypersensitivity (DTH) reactions involving oedema and granulocytic infiltration. The characteristic cytokines of Tc1 (gamma-interferon) and Tc2 (interleukins 4 and 5) are expressed in vivo during the DTH reaction. Tc1 cells that are deficient in cytokine synthesis also induce similar levels of DTH, supporting the lack of correlation between CD8+ T cell cytokine patterns and DTH. CD8+ T cells often produce lower cytokine levels than CD4 cells because the CD8 cells kill their antigen-presenting cells before full stimulation can occur. This effect can be counteracted by increasing the frequency of stimulation, or using perforin-deficient T cells. A multiparameter analysis of cytokine effects on CD8+ T cell differentiation has been initiated, on the basis of the principle that normal immune responses involve complex cytokine mixtures. All combinations of seven cytokines were tested. In some combinations, the combined effect could not have been predicted from individual cytokine functions. Conditions were identified in which each of interleukins 4, 10 and 12 could have opposite effects on CD8+ T cell differentiation.

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