Laboratory of Adaptive Immunity, Department of Translational Medicine, University of Milan, I.R.C.C.S. Istituto Clinico Humanitas, 20089, Rozzano, Milan, Italy.
Curr Top Microbiol Immunol. 2010;340:109-22. doi: 10.1007/978-3-642-03858-7_6.
The immunological synapse is a dynamic structure, formed between a T cell and one or more antigen-presenting cells, characterized by lipid and protein segregation, signaling compartmentalization, and bidirectional information exchange through soluble and membrane-bound transmitters. In addition, the immunological synapse is the site where signals delivered by the T-cell receptors, adhesion molecules, as well as costimulatory and coinhibitory receptors are decoded and integrated. Signaling modulation and tunable activation thresholds allow T cells to interpret the context in which the antigen is presented, recognize infectious stimuli, and finally decide between activation and tolerance. In this review, we discuss some strategies used by membrane receptors to tune activation signals in T cells.
免疫突触是一种动态结构,在 T 细胞和一个或多个抗原呈递细胞之间形成,其特征是脂质和蛋白质的分隔、信号的分隔化,以及通过可溶性和膜结合的递质进行的双向信息交换。此外,免疫突触是 T 细胞受体、黏附分子以及共刺激和共抑制受体传递的信号被解码和整合的部位。信号调节和可调的激活阈值使 T 细胞能够解释抗原呈递的背景,识别感染性刺激,并最终在激活和耐受之间做出决定。在这篇综述中,我们讨论了膜受体用于调节 T 细胞激活信号的一些策略。