Molecular and functional heterogeneity of IL-10-producing CD4+ T cells

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作者
Leonie Brockmann
Shiwa Soukou
Babett Steglich
Paulo Czarnewski
Lilan Zhao
Sandra Wende
Tanja Bedke
Can Ergen
Carolin Manthey
Theodora Agalioti
Maria Geffken
Oliver Seiz
Sara M. Parigi
Chiara Sorini
Jens Geginat
Keishi Fujio
Thomas Jacobs
Thomas Roesch
Jacob R. Izbicki
Ansgar W. Lohse
Richard A. Flavell
Christian Krebs
Jan-Ake Gustafsson
Per Antonson
Maria Grazia Roncarolo
Eduardo J. Villablanca
Nicola Gagliani
Samuel Huber
机构
[1] University Medical Center Hamburg-Eppendorf,I. Department of Medicine
[2] University Medical Center Hamburg-Eppendorf,Department of General, Visceral and Thoracic Surgery
[3] Karolinska Institute and University Hospital,Immunology and Allergy Unit, Department of Medicine, Solna
[4] Institute of Transfusion Medicine,Department of Allergy and Rheumatology, Graduate School of Medicine
[5] University Medical Center Hamburg-Eppendorf,Department of Immunology
[6] INGM-National Institute of Molecular Genetics “Romeo ed Enrica Invernizzi”,Department for Interdisciplinary Endoscopy
[7] The University of Tokyo,Department of Immunobiology, School of Medicine
[8] Bernhard-Nocht-Institute of Tropical Medicine,III. Department of Medicine
[9] University Medical Center Hamburg-Eppendorf,Department of Biosciences and Nutrition
[10] Yale University,Division of Stem Cell Transplantation and Regenerative Medicine, Department of Pediatrics
[11] Howard Hughes Medical Institute,undefined
[12] Yale University School of Medicine,undefined
[13] University Medical Center Hamburg-Eppendorf,undefined
[14] Karolinska Institutet,undefined
[15] ISCBRM,undefined
[16] Stanford School of Medicine,undefined
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摘要
IL-10 is a prototypical anti-inflammatory cytokine, which is fundamental to the maintenance of immune homeostasis, especially in the intestine. There is an assumption that cells producing IL-10 have an immunoregulatory function. However, here we report that IL-10-producing CD4+ T cells are phenotypically and functionally heterogeneous. By combining single cell transcriptome and functional analyses, we identified a subpopulation of IL-10-producing Foxp3neg CD4+ T cells that displays regulatory activity unlike other IL-10-producing CD4+ T cells, which are unexpectedly pro-inflammatory. The combinatorial expression of co-inhibitory receptors is sufficient to discriminate IL-10-producing CD4+ T cells with regulatory function from others and to identify them across different tissues and disease models in mice and humans. These regulatory IL-10-producing Foxp3neg CD4+ T cells have a unique transcriptional program, which goes beyond the regulation of IL-10 expression. Finally, we found that patients with Inflammatory Bowel Disease demonstrate a deficiency in this specific regulatory T-cell subpopulation.
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