首页> 美国卫生研究院文献>The Journal of Experimental Medicine >Phenotypic and functional alteration of CD4+ T cells after antigen stimulation. Resolution of two populations of memory T cells that both secrete interleukin 4
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Phenotypic and functional alteration of CD4+ T cells after antigen stimulation. Resolution of two populations of memory T cells that both secrete interleukin 4

机译:抗原刺激后CD4 + T细胞的表型和功能改变。两个都分泌白介素4的记忆T细胞群体的解析

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摘要

Phenotypic and functional alteration of murine CD4+ T cells after antigenic stimulation was studied using two anti-T cell mAbs recently described that define four distinct T cell subsets. Activation of T cells resulted in the permanent loss of 3G11 expression. However, two phenotypically distinct memory T cell populations were established depending on the system used; whereas those for anti-KLH antibody response were enriched in the fraction expression 6C10 (Fr. III), memory T cells for the allogeneic MLR lacked such expression (Fr. IV). Furthermore, successive stimulation with antigen in vitro resulted in secretion of IL-4 without detectable IL-2. This alteration of phenotype and interleukin secretion was also demonstrable when starting with 3G11+6C10- cells (Fr. I), the fraction that secretes IL-2 exclusively upon activation.
机译:使用最近描述的两种定义四个不同T细胞亚群的抗T细胞单克隆抗体,研究了抗原刺激后鼠CD4 + T细胞的表型和功能改变。 T细胞的激活导致3G11表达的永久丧失。然而,根据所使用的系统,建立了两个在表型上不同的记忆T细胞群。而抗KLH抗体应答的那些则富含6C10级分表达(图三),同种MLR的记忆T细胞则缺乏这种表达(图四)。此外,在体外连续用抗原刺激导致IL-4分泌而没有可检测的IL-2。当从3G11 + 6C10-细胞(图I)开始时,这种表型和白介素分泌的改变也被证实,这是在激活时专门分泌IL-2的部分。

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