固有层
生物
免疫系统
CD11c公司
促炎细胞因子
细胞生物学
免疫学
树突状细胞
人口
FOXP3型
白细胞介素
白细胞介素10
抗原提呈细胞
T细胞
细胞因子
炎症
医学
生物化学
表型
基因
环境卫生
上皮
遗传学
作者
Timothy L. Denning,Yichong Wang,Seema R. Patel,Ifor R. Williams,Bali Pulendran
出处
期刊:Nature Immunology
[Springer Nature]
日期:2007-09-16
卷期号:8 (10): 1086-1094
被引量:965
摘要
The intestinal immune system must elicit robust immunity against harmful pathogens but must also restrain immune responses directed against commensal microbes and dietary antigens. The mechanisms that maintain this dichotomy are poorly understood. Here we describe a population of CD11b+F4/80+CD11c- macrophages in the lamina propria that expressed several anti-inflammatory molecules, including interleukin 10 (IL-10), but little or no proinflammatory cytokines, even after stimulation with Toll-like receptor ligands. These macrophages induced, by a mechanism dependent on IL-10, retinoic acid and exogenous transforming growth factor-beta, the differentiation of Foxp3+ regulatory T cells. In contrast, lamina propria CD11b+ dendritic cells elicited IL-17 production. This IL-17 production was suppressed by lamina propria macrophages, indicating that a dynamic interaction between these subsets may influence the balance between immune activation and tolerance.
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