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The balance of power: innate lymphoid cells in tissue inflammation and repair
Jim G. Castellanos, Randy S. Longman
Jim G. Castellanos, Randy S. Longman
Published June 10, 2019
Citation Information: J Clin Invest. 2019;129(7):2640-2650. https://doi.org/10.1172/JCI124617.
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Review Series

The balance of power: innate lymphoid cells in tissue inflammation and repair

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Abstract

Over the last ten years, immunologists have recognized the central importance of an emerging group of innate lymphoid cells (ILCs) in health and disease. Characterization of these cells has provided a molecular definition of ILCs and their tissue-specific functions. Although the lineage-defining transcription factors, cytokine production, and nomenclature parallel those of T helper cells, ILCs do not require adaptive immune programming. Both environmental and host-derived signals shape the function of these evolutionarily ancient cells, which provide pathogen protection and promote tissue restoration. As such, ILCs function as a double-edged sword, balancing the inflammatory and reparative responses that arise during injury and disease. This Review highlights our recent understanding of tissue-resident ILCs and the signals that regulate their contribution to inflammation and tissue repair in health and disease.

Authors

Jim G. Castellanos, Randy S. Longman

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Figure 2

Tissue ILCs in chronic inflammation.

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Tissue ILCs in chronic inflammation.
Sustained activation of ILC effecto...
Sustained activation of ILC effector functions promote inflammation. Restorative functions of IL-22 can lead to aberrant epithelial proliferation and IL-18 production to sustain an inflammatory Th1 response. ILC2 responses recruit eosinophil effectors, trigger smooth muscle contraction, and promote fibrosis.

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