Wagner David H
Webb-Waring Institute, Department of Medicine, University of Colorado Denver and Health Sciences Center, 4200 East 9th Ave, Denver, CO, USA.
Clin Immunol. 2007 Apr;123(1):1-6. doi: 10.1016/j.clim.2006.08.006. Epub 2006 Sep 20.
Protection against the universe of pathogens requires a functional, diverse T cell repertoire. However, the price that is paid for an evolved, effective immune system includes the potential danger of generating autoaggressive T cells. Autoimmune diseases result from inherent breach of tolerance to self-antigens leading to disruption of the regulatory to autoaggressive T cell homeostatic balance. The immune system has evolved mechanisms to control those processes. For T cells, positive and negative selection in the thymus assures that only fully functional, non-self-reactive T cells will populate the periphery. Failure of this central tolerance would result in autoaggressive T cells escaping into the periphery. However, other means of escaping negative selection can occur in the periphery, i.e., TCR revision, or the altering of TCR expression after thymic egress. Here the potential benefits, i.e., expansion and re-shaping of the T cell repertoire as potentiated by TCR editing and revision are considered. Furthermore, the potential to develop autoaggressive TCR and thus enhance autoimmunity is considered.
抵御各种病原体需要一个功能健全、多样化的T细胞库。然而,进化出有效的免疫系统所付出的代价包括产生自身攻击性T细胞的潜在危险。自身免疫性疾病是由于对自身抗原的固有耐受性破坏,导致调节性T细胞与自身攻击性T细胞之间的稳态平衡被打破所致。免疫系统已经进化出控制这些过程的机制。对于T细胞来说,胸腺中的阳性和阴性选择确保只有功能完全正常、不具有自身反应性的T细胞才能进入外周。这种中枢耐受性的失败将导致自身攻击性T细胞逃逸到外周。然而,在外周也可能发生其他逃避阴性选择的方式,即TCR重排,或胸腺输出后TCR表达的改变。这里考虑了TCR编辑和重排所增强的T细胞库的潜在益处,即扩展和重塑。此外,还考虑了产生自身攻击性TCR从而增强自身免疫的可能性。