Gardner James M, Devoss Jason J, Friedman Rachel S, Wong David J, Tan Ying X, Zhou Xuyu, Johannes Kellsey P, Su Maureen A, Chang Howard Y, Krummel Matthew F, Anderson Mark S
Diabetes Center, University of California San Francisco (UCSF), San Francisco, CA 94122, USA.
Science. 2008 Aug 8;321(5890):843-7. doi: 10.1126/science.1159407.
The prevention of autoimmunity requires the elimination of self-reactive T cells during their development and maturation. The expression of diverse self-antigens by stromal cells in the thymus is essential to this process and depends, in part, on the activity of the autoimmune regulator (Aire) gene. Here we report the identification of extrathymic Aire-expressing cells (eTACs) resident within the secondary lymphoid organs. These stromally derived eTACs express a diverse array of distinct self-antigens and are capable of interacting with and deleting naïve autoreactive T cells. Using two-photon microscopy, we observed stable antigen-specific interactions between eTACs and autoreactive T cells. We propose that such a secondary network of self-antigen-expressing stromal cells may help reinforce immune tolerance by preventing the maturation of autoreactive T cells that escape thymic negative selection.
自身免疫的预防需要在自身反应性T细胞的发育和成熟过程中清除它们。胸腺基质细胞表达多种自身抗原对这一过程至关重要,并且部分依赖于自身免疫调节因子(Aire)基因的活性。在此,我们报告了在二级淋巴器官中存在的胸腺外表达Aire的细胞(eTACs)的鉴定。这些基质来源的eTACs表达多种不同的自身抗原,并且能够与幼稚的自身反应性T细胞相互作用并使其清除。使用双光子显微镜,我们观察到eTACs与自身反应性T细胞之间稳定的抗原特异性相互作用。我们提出,这样一个表达自身抗原的基质细胞二级网络可能通过阻止逃脱胸腺阴性选择的自身反应性T细胞成熟来帮助加强免疫耐受。