Crosstalk between ILC2s and Th2 CD4+ T Cells in Lung Disease

被引:4
|
作者
Mi, Lan-lan [1 ]
Guo, Wei-wei [1 ]
机构
[1] Shanghai Jiao Tong Univ, Shanghai Childrens Med Ctr, Dept Neonatol, Sch Med, Shanghai, Peoples R China
基金
中国国家自然科学基金;
关键词
INNATE LYMPHOID-CELLS; ALLERGIC AIRWAY INFLAMMATION; INCREASES SUSCEPTIBILITY; TYPE-2; INFLAMMATION; SEVERE ASTHMA; IFN-GAMMA; ACTIVATION; PROMOTES; DIFFERENTIATION; INTERLEUKIN-33;
D O I
10.1155/2022/8871037
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Cytokine secretion, such as interleukin-4 (IL-4), IL-5, IL-9, IL-13, and amphiregulin (Areg), by type 2 innate lymphoid cells (ILC2s) is indispensable for homeostasis, remodeling/repairing tissue structure, inflammation, and tumor immunity. Often viewed as the innate cell surrogate of T helper type 2 (Th2) cells, ILC2s not only secrete the same type 2 cytokines, but are also inextricably related to CD4(+)T cells in terms of cell origin and regulatory factors, bridging between innate and adaptive immunity. ILC2s interact with CD4(+)T cells to play a leading role in a variety of diseases through secretory factors. Here, we review the latest progress on ILC2s and CD4(+)T cells in the lung, the close relationship between the two, and their relevance in the lung disease and immunity. This literature review aids future research in pulmonary type 2 immune diseases and guides innovative treatment approaches for these diseases.
引用
收藏
页数:12
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