Conceptual Immunology Group, The Salk Institute for Biological Studies, 10010 North Torrey Pines Road, La Jolla, CA, 92037, USA,
Cell Mol Life Sci. 2014 Jun;71(11):2033-45. doi: 10.1007/s00018-013-1540-9. Epub 2013 Dec 14.
The existence of antigen-receptors, BCR, and T cell antigen-receptors, that are "polyreactive", necessitates a rethinking of its effect on two problems faced by the "adaptive" immune system: the self (S)-nonself (NS) discrimination and the determination of effector class. Here, we will concentrate on the impact of polyreactivity on the S-NS discrimination. The anti-S cells interacting with S (i.e., responding to Signal 1) are on the pathway to inactivation. Before irreversibility sets in, these cells can be activated by a second signal (Signal 2) from an effector T-helper (eTh). As these polyreactive anti-S cells express anti-NS specificities, they can be activated by recognition of NS-epitopes in the host's normal immunogenic load with the potential to result in autoimmunity. This problem is delineated using a discrete structural model, the corollaries of which are: (1) a two-step pathway for the purging of anti-S cells (i.e., the S-NS discrimination), and (2) defensible contexts within which to view the phenomena of receptor editing, anergy, and dual receptor cells.
抗原受体(BCR)和 T 细胞抗原受体的存在是“多反应性”的,这需要重新考虑其对“适应性”免疫系统面临的两个问题的影响:自我(S)-非自我(NS)的区分和效应器类别的确定。在这里,我们将集中讨论多反应性对 S-NS 区分的影响。与 S 相互作用的抗 S 细胞(即对信号 1 作出反应)处于失活途径中。在不可逆性发生之前,这些细胞可以被辅助性效应 T 细胞(eTh)的第二信号(信号 2)激活。由于这些多反应性的抗 S 细胞表达抗 NS 特异性,它们可以通过识别宿主正常免疫负荷中的 NS 表位被激活,从而有可能导致自身免疫。使用离散结构模型来描绘这个问题,其推论是:(1)清除抗 S 细胞(即 S-NS 区分)的两步途径;(2)在其中可以观察受体编辑、失能和双受体细胞等现象的有防御能力的上下文。