Reiner Steven L, Sallusto Federica, Lanzavecchia Antonio
Abramson Family Cancer Research Institute of the University of Pennsylvania, Philadelphia, PA 19104, USA.
Science. 2007 Aug 3;317(5838):622-5. doi: 10.1126/science.1143775.
In the course of the immune response against microbes, naïve T cells proliferate and generate varied classes of effector cells, as well as memory cells with distinct properties and functions. Owing to recent technological advances, some of the most imposing questions regarding effector and memory T cell differentiation are now becoming experimentally soluble: How many classes of antigen-specific T cells exist, and how malleable are they in their fate and in their functional state? How might a spectrum of cell fates be imparted to the clonal descendants of a single lymphocyte? Where, when, and how does pathogen-associated information refine the instruction, selection, and direction of newly activated T cells as they perform their tasks in different locations and times? Some surprising new glimpses ahead on these subjects and other yet-unanswered questions are discussed.
在针对微生物的免疫反应过程中,初始T细胞增殖并产生不同类别的效应细胞以及具有不同特性和功能的记忆细胞。由于最近的技术进步,一些关于效应T细胞和记忆T细胞分化的最具挑战性的问题现在正变得可以通过实验解决:存在多少类抗原特异性T细胞,它们在命运和功能状态上的可塑性如何?如何将一系列细胞命运赋予单个淋巴细胞的克隆后代?当新激活的T细胞在不同的时间和地点执行任务时,病原体相关信息在何处、何时以及如何完善对它们的指令、选择和引导?本文将讨论在这些主题以及其他尚未解答的问题上一些令人惊讶的新见解。