Tolerization of dendritic cells by TS cells:: the crucial role of inhibitory receptors ILT3 and ILT4

被引:631
作者
Chang, CC
Ciubotariu, R
Manavalan, JS
Yuan, J
Colovai, AI
Piazza, F
Lederman, S
Colonna, M
Cortesini, R
Dalla-Favera, R
Suciu-Foca, N [1 ]
机构
[1] Columbia Univ, Dept Pathol, New York, NY 10032 USA
[2] Columbia Univ, Lab Mol Immunol, New York, NY 10032 USA
[3] Washington Univ, Sch Med, St Louis, MO 63110 USA
[4] Univ Roma La Sapienza, Rome, Italy
基金
美国国家卫生研究院;
关键词
D O I
10.1038/ni760
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Immunoglobulin-like transcript 3 (ILT3) and ILT4 belong to a family of inhibitory receptors expressed by human monocytes and dendritic cells. We show here that CD8(+)CD28(-) alloantigen-specific T suppressor (T-S) cells induce the up-regulation of ILT3 and ILT4 on monocytes and dendritic cells, rendering these antigen-presenting cells (APCs) tolerogenic. Tolerogenic APCs show reduced expression of costimulatory molecules and induce antigen-specific unresponsiveness in CD4(+)T helper cells. Studies of human heart transplant recipients showed that rejection-free patients have circulating T-S cells, which induce the up-regulation of ILT3 and ILT4 in donor APCs. These findings demonstrate an important mechanism of immune regulation.
引用
收藏
页码:237 / 243
页数:7
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