Laboratory of Immunogenetics, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Rockville, Maryland 20852, USA.
Nat Rev Immunol. 2010 Nov;10(11):767-77. doi: 10.1038/nri2853. Epub 2010 Oct 11.
B cells are selected by the binding of antigen to clonally distributed B cell receptors (BCRs), triggering signalling cascades that result in B cell activation. With the recent application of high-resolution live-cell imaging, we are gaining an understanding of the events that initiate BCR signalling within seconds of its engagement with antigen. These observations are providing a molecular explanation for fundamental aspects of B cell responses, including antigen affinity discrimination and the value of class switching, as well as insights into the underlying causes of B cell tumorigenesis. Advances in our understanding of the earliest molecular events that follow antigen binding to the BCR may provide a general framework for the initiation of signalling in the adaptive immune system.
B 细胞通过抗原与克隆分布的 B 细胞受体(BCR)的结合被选择,触发信号级联反应,导致 B 细胞激活。最近应用高分辨率活细胞成像技术,我们正在了解 BCR 与抗原结合后几秒钟内启动 BCR 信号的事件。这些观察结果为 B 细胞反应的基本方面提供了分子解释,包括抗原亲和力的区分和类别转换的价值,以及对 B 细胞肿瘤发生的潜在原因的深入了解。对 BCR 与抗原结合后最早的分子事件的理解的进展,可能为适应性免疫系统信号的起始提供一个通用框架。