Department of Cancer Immunology and AIDS, Dana Farber Cancer Institute, Boston, USA.
Trends Immunol. 2011 Jan;32(1):12-8. doi: 10.1016/j.it.2010.11.002. Epub 2010 Dec 10.
Research into how self-reactive T cells are tolerized in lymph nodes has focused largely on dendritic cells (DCs). We now know that lymph node stromal cells (LNSC) are important mediators of deletional tolerance to peripheral tissue-restricted antigens (PTAs), which are constitutively expressed and presented by LNSCs. Of the major LNSC subsets, fibroblastic reticular cells and lymphatic endothelial cells are known to directly induce tolerance of responding naïve CD8 T cells. The biological outcome of this interaction fills a void otherwise not covered by DCs or thymic stromal cells. These findings, we suggest, necessitate a broadening of peripheral tolerance theory to include steady-state presentation of clinically relevant PTA to naïve CD8 T cells by lymph node-resident stroma.
针对淋巴结中自身反应性 T 细胞如何被耐受的研究主要集中在树突状细胞(DCs)上。我们现在知道,淋巴结基质细胞(LNSC)是外周组织限制性抗原(PTAs)缺失性耐受的重要介质,这些抗原由 LNSC 组成型表达和呈递。在主要的 LNSC 亚群中,成纤维网状细胞和淋巴管内皮细胞被认为可以直接诱导应答性幼稚 CD8 T 细胞的耐受。这种相互作用的生物学结果填补了 DCs 或胸腺基质细胞未涵盖的空白。我们认为,这些发现需要拓宽外周耐受理论,将临床相关 PTA 的稳态呈递给淋巴结驻留基质中的幼稚 CD8 T 细胞包括在内。