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

Leonie Brockmann(Universität Hamburg), Shiwa Soukou(Universität Hamburg), Babett Steglich(Universität Hamburg), Paulo Czarnewski(Karolinska University Hospital), Lilan Zhao(Universität Hamburg), Sandra Wende(Universität Hamburg), Tanja Bedke(Universität Hamburg), Can Ergen(Universität Hamburg), Carolin Manthey(Universität Hamburg), Theodora Agalioti(Universität Hamburg), Maria Geffken(Universität Hamburg), Oliver Seiz(Universität Hamburg), Sara Martina Parigi(Karolinska University Hospital), Chiara Sorini(Karolinska University Hospital), Jens Geginat(Istituto Nazionale Genetica Molecolare), Keishi Fujio(The University of Tokyo), Thomas Jacobs(Bernhard Nocht Institute for Tropical Medicine), Thomas Röesch(Universität Hamburg), Jacob R. Izbicki(Universität Hamburg), Ansgar W. Lohse(Universität Hamburg), Richard A. Flavell(Howard Hughes Medical Institute), Christian F. Krebs(Universität Hamburg), Jan-Åke Gustafsson(Karolinska Institutet), Per Antonson(Karolinska Institutet), Maria Grazia Roncarolo(Stanford Medicine), Eduardo J. Villablanca(Karolinska University Hospital), Nicola Gagliani(Karolinska University Hospital), Samuel Huber(Universität Hamburg)
Nature Communications
December 18, 2018
Cited by 135Open Access
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Abstract

Abstract 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 Foxp3 neg 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 Foxp3 neg 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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