Lung ILC2s link innate and adaptive responses in allergic inflammation

被引:148
作者
Martinez-Gonzalez, Itziar [1 ]
Steer, Catherine A. [1 ,2 ]
Takei, Fumio [1 ,3 ]
机构
[1] British Columbia Canc Agcy, Terry Fox Lab, Vancouver, BC V5Z 1L3, Canada
[2] Univ British Columbia, Interdisciplinary Oncol Program, Vancouver, BC V5Z 1L3, Canada
[3] Univ British Columbia, Dept Pathol & Lab Med, Vancouver, BC V5Z 1L3, Canada
关键词
NATURAL HELPER-CELLS; LYMPHOID-CELLS; IMMUNE-RESPONSES; TYPE-2; IMMUNITY; URIC-ACID; IN-VIVO; IL-33; IL-25; CYTOKINES; SYSTEM;
D O I
10.1016/j.it.2015.01.005
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
How allergens trigger the T helper 2 (Th2) response that characterizes allergic lung inflammation is not well understood. Epithelium-derived alarmins released after an allergen encounter activate the innate immune system, including group 2 innate lymphoid cells (ILC2s) which produce the type 2 interleukins IL-5 and IL-13. It has been recently shown that ILC2-derived cytokines are responsible not only for the innate responses underlying allergic inflammation but also for the initiation of the adaptive Th2 response. We review the role of lung ILC2s in the development of allergic inflammation and, in the context of recent findings, propose a common pathway wherein, ILC2s, activated by the epithelium-derived cytokine IL-33, link the innate and the adaptive responses after allergen encounter in the lung.
引用
收藏
页码:189 / 195
页数:7
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