Inflammatory migration-associated skin-like CD103+ ILC2s impact lung immunity 9270

Abstract Description Group 2 innate lymphoid cells (ILC2s) are tissue-resident cells with transcriptional signatures imprinted by tissues in which they reside. Post-inflammatory expansion, migration and protective roles in distant organs have been described for small intestinal and bone marrow ILC2s, but whether additional barrier ILC2s perform similar roles is unknown. We show that skin ILC2s (skILC2s) expand after infestation by commensal hair-follicle mites, enter the blood and adapt to lung residence while enabling new innate sources of IL-13 and IL-17A. We use immunohistochemistry to define positioning of newly recruited ex-skILCs and challenges with migratory helminths and influenza to demonstrate impacts on lung host defense. Redistribution of barrier ILC2s educated by exposure to microbiota and foreign antigens may be an intrinsic property of the innate immune system designed to enhance internal organ responses during transition to the post-birth environment. Topic Categories Mucosal and Regional Immunology (MUC)

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Publication Details

Journal
The Journal of Immunology
Published
2025-11-01
DOI
https://doi.org/10.1093/jimmun/vkaf283.2693
Primary Topic
IL-33, ST2, and ILC Pathways
Type
article
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article

Inflammatory migration-associated skin-like CD103+ ILC2s impact lung immunity 9270

Tithi Roy, Lian Mi, Richard M. Locksley, Roberto R. Ricardo-González et al.
The Journal of Immunology
IL-33, ST2, and ILC Pathways
article

Inflammatory migration-associated skin-like CD103+ ILC2s impact lung immunity 9270

Tithi Roy, Lian Mi, Richard M. Locksley, Roberto R. Ricardo-González, Hong-Erh Liang
article en

Abstract

Abstract Description Group 2 innate lymphoid cells (ILC2s) are tissue-resident cells with transcriptional signatures imprinted by tissues in which they reside. Post-inflammatory expansion, migration and protective roles in distant organs have been described for small intestinal and bone marrow ILC2s, but whether additional barrier ILC2s perform similar roles is unknown. We show that skin ILC2s (skILC2s) expand after infestation by commensal hair-follicle mites, enter the blood and adapt to lung residence while enabling new innate sources of IL-13 and IL-17A. We use immunohistochemistry to define positioning of newly recruited ex-skILCs and challenges with migratory helminths and influenza to demonstrate impacts on lung host defense. Redistribution of barrier ILC2s educated by exposure to microbiota and foreign antigens may be an intrinsic property of the innate immune system designed to enhance internal organ responses during transition to the post-birth environment. Topic Categories Mucosal and Regional Immunology (MUC)

The Journal of ImmunologyVol. 214(Supplement_1)
University of California, San Francisco (US), University of San Francisco (US)
Openalex Percentile: Top 62%
IL-33, ST2, and ILC Pathways
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