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CD28/B7共刺激在人Th2细胞因子产生细胞发育中的关键作用。

Critical role of CD28/B7 costimulation in the development of human Th2 cytokine-producing cells.

作者信息

Webb L M, Feldmann M

机构信息

Kennedy Institute of Rheumatology, Sunley Division, Hammersmith, London, UK.

出版信息

Blood. 1995 Nov 1;86(9):3479-86.

PMID:7579453
Abstract

CD28 is a major costimulatory signal receptor for T cells. We have used human naive CD4+ cells from cord blood to analyze the effect of the CD28/B7 costimulatory pathway on development of T helper (Th) subsets. We show that CD28 costimulation is critical for development of the Th2 cytokine-producing cells and that in the absence of CD28 costimulation, cells are not primed to produce Th2 cytokines and consequently "default" to the Th1 subset, independent of the presence of exogenous cytokines. After CD28 costimulation, cells differentiate into a subset that produces Th2 cytokines. However, further CD28 costimulation is not required to maintain Th2 cytokine production. We conclude that D28 costimulation is critical for the development of Th0 and Th2 subsets, but not for the maintenance of cytokine production.

摘要

CD28是T细胞的主要共刺激信号受体。我们利用来自脐带血的人类初始CD4+细胞来分析CD28/B7共刺激途径对辅助性T细胞(Th)亚群发育的影响。我们发现,CD28共刺激对于产生Th2细胞因子的细胞的发育至关重要,并且在没有CD28共刺激的情况下,细胞不会被启动产生Th2细胞因子,因此会“默认”分化为Th1亚群,这与外源性细胞因子的存在无关。在CD28共刺激后,细胞分化为产生Th2细胞因子的亚群。然而,维持Th2细胞因子的产生并不需要进一步的CD28共刺激。我们得出结论,CD28共刺激对于Th0和Th2亚群的发育至关重要,但对于细胞因子产生的维持并非必需。

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