The Walter and Eliza Hall Institute of Medical Research, Parkville, Victoria, Australia; Department of Medical Biology, The University of Melbourne, Parkville, Victoria, Australia.
Division of Cell Signalling and Immunology, School of Life Sciences, University of Dundee, Dundee, UK.
Curr Opin Immunol. 2018 Apr;51:32-38. doi: 10.1016/j.coi.2018.01.002. Epub 2018 Feb 3.
Activation induced proliferation and clonal expansion of antigen specific lymphocytes is a hallmark of the adaptive immune response to pathogens. Recent studies identify two distinct control phases. In the first T and B lymphocytes integrate antigen and additional costimuli to motivate a programmed proliferative burst that ceases with a return to cell quiescence and eventual death. This proliferative burst is autonomously timed, ensuring an appropriate response magnitude whilst preventing uncontrolled expansion. This initial response is subject to further modification and extension by a range of signals that modify, expand and direct the emergence of a rich array of new cell types. Thus, both robust clonal expansion of a small number of antigen specific T cells, and the concurrent emergence of extensive cellular diversity, confers immunity to a vast array of different pathogens. The in vivo response to a given pathogen is made up by the sum of all responding clones and is reproducible and pathogen specific. Thus, a precise description of the regulatory principles governing lymphocyte proliferation, differentiation and survival is essential to a unified understanding of the immune system.
抗原特异性淋巴细胞的激活诱导增殖和克隆扩增是病原体适应性免疫反应的标志。最近的研究确定了两个不同的控制阶段。在第一阶段,T 和 B 淋巴细胞整合抗原和其他共刺激物,以激发程序性增殖爆发,当细胞回到静止状态并最终死亡时,增殖爆发就会停止。这种增殖爆发是自主定时的,确保了适当的反应幅度,同时防止了不受控制的扩增。最初的反应受到一系列信号的进一步修饰和扩展,这些信号修饰、扩展并指导了大量新细胞类型的出现。因此,少量抗原特异性 T 细胞的强烈克隆扩增,以及同时出现的广泛细胞多样性,赋予了对大量不同病原体的免疫力。对给定病原体的体内反应是由所有反应克隆的总和组成的,并且是可重复的和病原体特异性的。因此,精确描述调节淋巴细胞增殖、分化和存活的调控原则对于统一理解免疫系统至关重要。