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Choice of resident costimulatory molecule can influence cell fate in human naive CD4+ T cell differentiation.

机译:常驻共刺激分子的选择可影响人类幼稚CD4 + T细胞分化中的细胞命运。

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With antigen stimulation, naive CD4+ T cells differentiate to several effector or memory cell populations, and cytokines contribute to differentiation outcome. Several proteins on these cells receive costimulatory signals, but a systematic comparison of their differential effects on naive T cell differentiation has not been conducted. Two costimulatory proteins, CD28 and ICAM-1, resident on human naive CD4+ T cells were compared for participation in differentiation. Under controlled conditions, and with no added cytokines, costimulation through either CD3+CD28 or CD3+CAM-1 induced differentiation to T effector and T memory cells. In contrast, costimulation through CD3+ICAM-1 induced differentiation to Treg cells whereas costimulation through CD3+CD28 did not.
机译:通过抗原刺激,幼稚的CD4 + T细胞可分化为几个效应子或记忆细胞群,而细胞因子则有助于分化。这些细胞上的几种蛋白质会接受共刺激信号,但是尚未对它们对幼稚T细胞分化的不同作用进行系统比较。比较了驻留在人类幼稚CD4 + T细胞上的两种共刺激蛋白CD28和ICAM-1参与分化的过程。在受控条件下,并且不添加细胞因子,通过CD3 + CD28或CD3 + CAM-1的共刺激诱导分化为T效应细胞和T记忆细胞。相反,通过CD3 + ICAM-1的共刺激可诱导向Treg细胞的分化,而通过CD3 + CD28的共刺激则不会。

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