Non-redundant functions of group 2 innate lymphoid cells

被引:0
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作者
Katja J. Jarick
Patrycja M. Topczewska
Manuel O. Jakob
Hiroshi Yano
Mohammad Arifuzzaman
Xuemei Gao
Sotiria Boulekou
Vladislava Stokic-Trtica
Pierre S. Leclère
Alexandra Preußer
Zoe A. Rompe
Anton Stamm
Amy M. Tsou
Coco Chu
Frederik R. Heinrich
Gabriela M. Guerra
Pawel Durek
Andranik Ivanov
Dieter Beule
Sofia Helfrich
Claudia U. Duerr
Anja A. Kühl
Christina Stehle
Chiara Romagnani
Mir-Farzin Mashreghi
Andreas Diefenbach
David Artis
Christoph S. N. Klose
机构
[1] Charité–Universitätsmedizin Berlin,Department of Microbiology, Infectious Diseases and Immunology
[2] Corporate Member of Freie Universität Berlin and Humboldt-Universität zu Berlin,Jill Roberts Institute for Research in Inflammatory Bowel Disease
[3] Weill Cornell Medicine,Joan and Sanford I. Weill Department of Medicine, Division of Gastroenterology and Hepatology
[4] Weill Cornell Medicine,Department of Microbiology and Immunology
[5] Cornell University,Division of Pediatric Gastroenterology, Hepatology and Nutrition
[6] Weill Cornell Medicine,Deutsches Rheuma
[7] Cornell University,Forschungszentrum (DRFZ)
[8] Weill Cornell Medical College,Core Unit Bioinformatics
[9] an Institute of the Leibniz Association,iPATH.Berlin – Core Unit of the Charité Universitätsmedizin Berlin
[10] Berlin Institute of Health at Charité–Universitätsmedizin Berlin,Charité – Universitätsmedizin Berlin, corporate member of Freie Universität Berlin and Humboldt
[11] Corporate Member of Freie Universität Berlin and Humboldt-Universität zu Berlin,Universität zu Berlin
[12] Department of Gastroenterology,Friedman Center for Nutrition and Inflammation, Joan and Sanford I. Weill Department of Medicine, Department of Microbiology and Immunology, Weill Cornell Medicine
[13] Infectious Diseases and Rheumatology,undefined
[14] Hindenburgdamm 30,undefined
[15] 12203,undefined
[16] Leibniz–Science Campus Chronic Inflammation,undefined
[17] Cornell University,undefined
来源
Nature | 2022年 / 611卷
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摘要
Protective immunity relies on the interplay of innate and adaptive immune cells with complementary and redundant functions. Innate lymphoid cells (ILCs) have recently emerged as tissue-resident, innate mirror images of the T cell system, with which they share lineage-specifying transcription factors and effector machinery1. Located at barrier surfaces, ILCs are among the first responders against invading pathogens and thus could potentially determine the outcome of the immune response2. However, so far it has not been possible to dissect the unique contributions of ILCs to protective immunity owing to limitations in specific targeting of ILC subsets. Thus, all of the available data have been generated either in mice lacking the adaptive immune system or with tools that also affect other immune cell subsets. In addition, it has been proposed that ILCs might be dispensable for a proper immune response because other immune cells could compensate for their absence3–7. Here we report the generation of a mouse model based on the neuromedin U receptor 1 (Nmur1) promoter as a driver for simultaneous expression of Cre recombinase and green fluorescent protein, which enables gene targeting in group 2 ILCs (ILC2s) without affecting other innate and adaptive immune cells. Using Cre-mediated gene deletion of Id2 and Gata3 in Nmur1-expressing cells, we generated mice with a selective and specific deficiency in ILC2s. ILC2-deficient mice have decreased eosinophil counts at steady state and are unable to recruit eosinophils to the airways in models of allergic asthma. Further, ILC2-deficient mice do not mount an appropriate immune and epithelial type 2 response, resulting in a profound defect in worm expulsion and a non-protective type 3 immune response. In total, our data establish non-redundant functions for ILC2s in the presence of adaptive immune cells at steady state and during disease and argue for a multilayered organization of the immune system on the basis of a spatiotemporal division of labour.
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页码:794 / 800
页数:6
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