Lymph node stroma broaden the peripheral tolerance paradigm

被引:88
作者
Fletcher, Anne L. [1 ]
Malhotra, Deepali [1 ]
Turley, Shannon J. [1 ,2 ]
机构
[1] Dana Farber Canc Inst, Dept Canc Immunol & AIDS, Boston, MA 02115 USA
[2] Harvard Univ, Sch Med, Dept Pathol, Boston, MA 02115 USA
关键词
FIBROBLASTIC RETICULAR CELLS; ORGAN-SPECIFIC AUTOIMMUNITY; FOLLICULAR DENDRITIC CELLS; THYMIC EPITHELIAL-CELLS; T-CELLS; GENE-EXPRESSION; IMMUNOLOGICAL-TOLERANCE; INFLAMMATORY DISEASES; ANTIGEN PRESENTATION; STEADY-STATE;
D O I
10.1016/j.it.2010.11.002
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
071005 [微生物学]; 100108 [医学免疫学];
摘要
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 naive 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 naive CD8 T cells by lymph node-resident stroma.
引用
收藏
页码:12 / 18
页数:7
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