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Innate lymphoid cells as regulators of immunity, inflammation and tissue homeostasis

Nature Immunology volume 17, pages 765–774 (2016)Cite this article

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Abstract

Research over the last 7 years has led to the formal identification of innate lymphoid cells (ILCs), increased the understanding of their tissue distribution and has established essential functions of ILCs in diverse physiological processes. These include resistance to pathogens, the regulation of autoimmune inflammation, tissue remodeling, cancer and metabolic homeostasis. Notably, many ILC functions appear to be regulated by mechanisms distinct from those of other innate and adaptive immune cells. In this Review, we focus on how group 2 ILC (ILC2) and group 3 ILC (ILC3) responses are regulated and how these cells interact with other immune and non-immune cells to mediate their functions. We highlight experimental evidence from mouse models and patient-based studies that have elucidated the effects of ILCs on the maintenance of tissue homeostasis and the consequences for health and disease.

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Figure 1: The distribution of ILCs at the mucosa of the intestine.
Figure 2: Integration of ILC2s in the type 2 immune response.
Figure 3: ILC3 responses at epithelial barriers.

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Acknowledgements

We thank T. Mahlakoiv, L.C. Rankin and A.-L. Flamar for critical reading of the manuscript. Supported by the US National Institutes of Health (AI061570, AI087990, AI074878, AI083480, AI095466, AI095608, AI102942, and AI097333 for the Artis laboratory), the Burroughs Wellcome Fund (Artis laboratory) and the Crohn's & Colitis Foundation of America (Artis laboratory).

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  1. Joan and Sanford I. Weill Department of Medicine, Department of Microbiology and Immunology, Jill Roberts Institute for Research in Inflammatory Bowel Disease, Weill Cornell Medicine, Cornell University, New York, New York, USA

    Christoph S N Klose & David Artis

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Correspondence to David Artis.

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Klose, C., Artis, D. Innate lymphoid cells as regulators of immunity, inflammation and tissue homeostasis. Nat Immunol 17, 765–774 (2016). https://doi.org/10.1038/ni.3489

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