Suppr超能文献

抗原刺激的持续时间决定了初始T细胞和效应T细胞的命运。

The duration of antigenic stimulation determines the fate of naive and effector T cells.

作者信息

Iezzi G, Karjalainen K, Lanzavecchia A

机构信息

Basel Institute for Immunology, Switzerland.

出版信息

Immunity. 1998 Jan;8(1):89-95. doi: 10.1016/s1074-7613(00)80461-6.

Abstract

It is known that T cells engage antigen-presenting cells (APCs) in a stable interaction that results in sustained TCR signaling. We show here that the duration of this process is critical in determining whether T cells will be activated or deleted. Whereas naive T cells require approximately 20 hr of sustained signaling to be committed to proliferation, effector T cells become committed after only 1 hr but die following activation if antigenic stimulation is prolonged. Costimulation by anti-CD28 facilitates T cell activation by decreasing the time of commitment and by protecting T cells from death. These findings explain in quantitative terms the essential requirement for professional APCs in T cell priming and show that the duration of antigenic stimulation is the major factor determining the fate of naive and effector T cells.

摘要

已知T细胞与抗原呈递细胞(APC)进行稳定的相互作用,从而产生持续的TCR信号传导。我们在此表明,这一过程的持续时间对于决定T细胞是被激活还是被清除至关重要。初始T细胞需要约20小时的持续信号传导才能进入增殖状态,而效应T细胞仅在1小时后就进入增殖状态,但如果抗原刺激延长,激活后则会死亡。抗CD28共刺激通过缩短进入增殖状态的时间和保护T细胞免于死亡来促进T细胞激活。这些发现从定量角度解释了专职APC在T细胞致敏中的基本需求,并表明抗原刺激的持续时间是决定初始T细胞和效应T细胞命运的主要因素。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验