先天性淋巴细胞
免疫学
过敏原
过敏性炎症
细胞因子
炎症
过敏
生物
免疫球蛋白E
肺
白细胞介素13
白细胞介素4
医学
先天免疫系统
免疫系统
内科学
抗体
作者
Itziar Martínez-González,Laura Mathä,Catherine A. Steer,Maryam Ghaedi,Grace F. T. Poon,Fumio Takei
出处
期刊:Immunity
[Elsevier]
日期:2016-07-01
卷期号:45 (1): 198-208
被引量:211
标识
DOI:10.1016/j.immuni.2016.06.017
摘要
Group 2 innate lymphoid cells (ILC2s) in the lung are stimulated by inhaled allergens. ILC2s do not directly recognize allergens but they are stimulated by cytokines including interleukin (IL)-33 released by damaged epithelium. In response to allergens, lung ILC2s produce T helper 2 cell type cytokines inducing T cell-independent allergic lung inflammation. Here we examined the fate of lung ILC2s upon allergen challenges. ILC2s proliferated and secreted cytokines upon initial stimulation with allergen or IL-33, and this phase was followed by a contraction phase as cytokine production ceased. Some ILC2s persisted long after the resolution of the inflammation as allergen-experienced ILC2s and responded to unrelated allergens more potently than naive ILC2s, mediating severe allergic inflammation. The allergen-experienced ILC2s exhibited a gene expression profile similar to that of memory T cells. The memory-like properties of allergen-experienced ILC2s may explain why asthma patients are often sensitized to multiple allergens.
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