Spatial regulation of IL-4 signalling in vivo

被引:16
作者
Redpath, Stephen A. [1 ]
Fieieis, Graham [1 ]
Perona-Wright, Georgia [1 ]
机构
[1] Univ British Columbia, Dept Microbiol & Immunol, Inst Life Sci, Vancouver, BC V6T 1Z3, Canada
基金
加拿大自然科学与工程研究理事会;
关键词
Co-infection; Bystander cells; Cytokine signalling; Cytokine location; IL-4; INNATE LYMPHOID-CELLS; PLASMODIUM-FALCIPARUM MALARIA; ALLERGIC LUNG INFLAMMATION; HELPER T-CELLS; DENDRITIC CELLS; HELMINTH INFECTION; RECEPTOR EXPRESSION; TYPE-2; IMMUNITY; TH2; POLARIZATION; INTERLEUKIN-4; RECEPTOR;
D O I
10.1016/j.cyto.2015.02.026
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Type 2 immune responses are defined by the cytokines interleukin 4 (IL-4), IL-5 and IL-13 and the cellular and physiological changes that these cytokines induce, including IgE production, eosinophilia, mast cell degranulation, mucus secretion and smooth muscle contraction. Together these responses provide a "weep and sweep" reflex that is optimised to expel parasitic worms. The same response can also be pathological when mis-timed or activated inappropriately. Current understanding of the orchestration and regulation of type 2 immunity is rapidly advancing, with recent identification of participating innate cells and elucidation of the cytokine signals responsible for their activation. In vivo, the outcome of cytokine signalling is critically dependent on timing, location and context. In this commentary, we describe the spatiotemporal control of type 2 cytokine signalling, consider its implications for bystander cells, and discuss its significance during co-infection. Crown Copyright (C) 2015 Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:51 / 56
页数:6
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