细胞生物学
抗原提呈细胞
白细胞介素2受体
ZAP70型
T细胞
生物
细胞毒性T细胞
免疫系统
自然杀伤性T细胞
抗原
白细胞介素21
自身免疫
T细胞受体
效应器
免疫学
C型凝集素
化学
分子生物学
体外
生物化学
作者
Sandra J. van Vliet,Sonja I. Gringhuis,Teunis B. H. Geijtenbeek,Yvette van Kooyk
出处
期刊:Nature Immunology
[Springer Nature]
日期:2006-09-24
卷期号:7 (11): 1200-1208
被引量:164
摘要
Homeostatic control of T cells involves tight regulation of effector T cells to prevent excessive activation that can cause tissue damage and autoimmunity. Little is known, however, about whether antigen-presenting cells (APCs) are also involved in maintaining immune system homeostasis once effector T cells are stimulated. Here we found that immature APCs downregulated effector T cell function by a mechanism involving the C-type lectin MGL expressed by APCs. Glycosylation-dependent interactions of MGL with CD45 on effector T cells negatively regulated T cell receptor-mediated signaling and T cell-dependent cytokine responses, which in turn decreased T cell proliferation and increased T cell death. Thus, regulation of effector T cells by MGL expressed on APCs may provide a target for regulating chronic inflammatory and autoimmune diseases.
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