Group 2 Innate Lymphoid Cells in Health and Disease
Author(s) -
Brian Kim,
David Artis
Publication year - 2015
Publication title -
cold spring harbor perspectives in biology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 6.011
H-Index - 173
ISSN - 1943-0264
DOI - 10.1101/cshperspect.a016337
Subject(s) - innate lymphoid cell , biology , immunology , gata3 , interleukin 33 , context (archaeology) , inflammation , immunity , progenitor cell , allergic inflammation , innate immune system , stem cell , microbiology and biotechnology , interleukin , cytokine , transcription factor , immune system , paleontology , biochemistry , gene
Group 2 innate lymphoid cells (ILC2s) play critical roles in anti-helminth immunity, airway epithelial repair, and metabolic homeostasis. Recently, these cells have also emerged as key players in the development of allergic inflammation at multiple barrier surfaces. ILC2s arise from common lymphoid progenitors in the bone marrow, are dependent on the transcription factors RORα, GATA3, and TCF-1, and produce the type 2 cytokines interleukin (IL)-4, IL-5, IL-9, and/or IL-13. The epithelial cell-derived cytokines IL-25, IL-33, and TSLP regulate the activation and effector functions of ILC2s, and recent studies suggest that their responsiveness to these cytokines and other factors may depend on their tissue environment. In this review, we focus on recent advances in our understanding of the various factors that regulate ILC2 function in the context of immunity, inflammation, and tissue repair across multiple organ systems.
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