先天性淋巴细胞
白细胞介素-7受体
免疫学
生物
先天免疫系统
人口
白细胞介素33
白细胞介素23
白细胞介素
炎症
白细胞介素2受体
白细胞介素17
细胞因子
T细胞
免疫系统
医学
环境卫生
作者
Jenny Mjösberg,Sara Trifari,Natasha K. Crellin,Charlotte P. Peters,Cornelis M. van Drunen,Berber Piet,Wytske J. Fokkens,Tom Cupedo,Hergen Spits
出处
期刊:Nature Immunology
[Springer Nature]
日期:2011-09-11
卷期号:12 (11): 1055-1062
被引量:1080
摘要
Innate lymphoid cells (ILCs) are emerging as a family of effectors and regulators of innate immunity and tissue remodeling. Interleukin 22 (IL-22)- and IL-17-producing ILCs, which depend on the transcription factor RORγt, express CD127 (IL-7 receptor α-chain) and the natural killer cell marker CD161. Here we describe another lineage-negative CD127(+)CD161(+) ILC population found in humans that expressed the chemoattractant receptor CRTH2. These cells responded in vitro to IL-2 plus IL-25 and IL-33 by producing IL-13. CRTH2(+) ILCs were present in fetal and adult lung and gut. In fetal gut, these cells expressed IL-13 but not IL-17 or IL-22. There was enrichment for CRTH2(+) ILCs in nasal polyps of chronic rhinosinusitis, a typical type 2 inflammatory disease. Our data identify a unique type of human ILC that provides an innate source of T helper type 2 (T(H)2) cytokines.
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