Nemazee D
Department of Immunology, Scripps Research Institute, La Jolla, California 92037, USA.
Annu Rev Immunol. 2000;18:19-51. doi: 10.1146/annurev.immunol.18.1.19.
The process of clonal selection is a central feature of the immune system, but immune specificity is also regulated by receptor selection, in which the fate of a lymphocyte's antigen receptor is uncoupled from that of the cell itself. Whereas clonal selection controls cell death or survival in response to antigen receptor signaling, receptor selection regulates the process of V(D)J recombination, which can alter or fix antigen receptor specificity. Receptor selection is carried out in both T and B cells and can occur at different stages of lymphocyte differentiation, in which it plays a key role in allelic exclusion, positive selection, receptor editing, and the diversification of the antigen receptor repertoire. Thus, the immune system takes advantage of its control of V(D)J recombination to modify antigen receptors in such a way that self/non-self discrimination is enhanced. New information about receptor editing in T cells and B-1 B cells is also discussed.
克隆选择过程是免疫系统的核心特征,但免疫特异性也受受体选择的调控,在受体选择过程中,淋巴细胞抗原受体的命运与其自身细胞的命运相互分离。克隆选择通过抗原受体信号传导来控制细胞死亡或存活,而受体选择则调节V(D)J重排过程,该过程可改变或固定抗原受体特异性。T细胞和B细胞均会进行受体选择,且可发生在淋巴细胞分化的不同阶段,在等位基因排斥、阳性选择、受体编辑以及抗原受体库的多样化过程中发挥关键作用。因此,免疫系统利用其对V(D)J重排的控制来修饰抗原受体,从而增强自身/非自身的辨别能力。本文还讨论了有关T细胞和B-1 B细胞中受体编辑的新信息。