دورية أكاديمية

Intestinal IFN-γ–producing type 1 regulatory T cells coexpress CCR5 and programmed cell death protein 1 and downregulate IL-10 in the inflamed guts of patients with inflammatory bowel disease

التفاصيل البيبلوغرافية
العنوان: Intestinal IFN-γ–producing type 1 regulatory T cells coexpress CCR5 and programmed cell death protein 1 and downregulate IL-10 in the inflamed guts of patients with inflammatory bowel disease
المؤلفون: Alfen J. S., Larghi P., Facciotti F., Gagliani N., Bosotti R., Paroni M., Maglie S., Gruarin P., Vasco C. M., Ranzani V., Frusteri C., Iseppon A., Moro M., Crosti M. C., Gatti S., Pagani M., Caprioli F., Abrignani S., Flavell R. A., Geginat J.
المساهمون: J.S. Alfen, P. Larghi, F. Facciotti, N. Gagliani, R. Bosotti, M. Paroni, S. Maglie, P. Gruarin, C.M. Vasco, V. Ranzani, C. Frusteri, A. Iseppon, M. Moro, M.C. Crosti, S. Gatti, M. Pagani, F. Caprioli, S. Abrignani, R.A. Flavell, J. Geginat
بيانات النشر: Elsevier
سنة النشر: 2018
المجموعة: The University of Milan: Archivio Istituzionale della Ricerca (AIR)
مصطلحات موضوعية: IL-10, IL-23, Inflammatory bowel disease, regulatory T cell, Adult, Aged, Animal, Cells, Cultured, Colonic Neoplasm, Cytokine, Female, Human, Intestinal Mucosa, Male, Mice, Inbred C57BL, Transgenic, Middle Aged, Programmed Cell Death 1 Receptor, Receptors, CCR5, T-Lymphocytes, Regulatory, Young Adult, Settore BIO/11 - Biologia Molecolare
الوصف: BACKGROUND: IL-10 is an anti-inflammatory cytokine required for intestinal immune homeostasis. It mediates suppression of T-cell responses by type 1 regulatory T (TR1) cells but is also produced by CD25+ regulatory T (Treg) cells. OBJECTIVE: We aimed to identify and characterize human intestinal TR1 cells and to investigate whether they are a relevant cellular source of IL-10 in patients with inflammatory bowel diseases (IBDs). METHODS: CD4+ T cells isolated from the intestinal lamina propria of human subjects and mice were analyzed for phenotype, cytokine production, and suppressive capacities. Intracellular IL-10 expression by CD4+ T-cell subsets in the inflamed guts of patients with IBD (Crohn disease or ulcerative colitis) was compared with that in cells from noninflamed control subjects. Finally, the effects of proinflammatory cytokines on T-cell IL-10 expression were analyzed, and IL-1β and IL-23 responsiveness was assessed. RESULTS: Intestinal TR1 cells could be identified by coexpression of CCR5 and programmed cell death protein 1 (PD-1) in human subjects and mice. CCR5+PD-1+ TR1 cells expressed IFN-γ and efficiently suppressed T-cell proliferation and transfer colitis. Intestinal IFN-γ+ TR1 cells, but not IL-7 receptor-positive TH cells or CD25+ Treg cells, showed lower IL-10 expression in patients with IBDs. TR1 cells were responsive to IL-23, and IFN-γ+ TR1 cells downregulated IL-10 with IL-1β and IL-23. Conversely, CD25+ Treg cells expressed higher levels of IL-1 receptor but showed stable IL-10 expression. CONCLUSIONS: We provide the first ex vivo characterization of human intestinal TR1 cells. Selective downregulation of IL-10 by IFN-γ+ TR1 cells in response to proinflammatory cytokines is likely to drive excessive intestinal inflammation in patients with IBDs.
نوع الوثيقة: article in journal/newspaper
اللغة: English
العلاقة: info:eu-repo/semantics/altIdentifier/pmid/29369775; info:eu-repo/semantics/altIdentifier/wos/WOS:000449429800017; volume:142; issue:5; firstpage:1537; lastpage:1547; numberofpages:11; journal:JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY; http://hdl.handle.net/2434/693050Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85042181305
DOI: 10.1016/j.jaci.2017.12.984
الإتاحة: https://doi.org/10.1016/j.jaci.2017.12.984Test
http://hdl.handle.net/2434/693050Test
حقوق: info:eu-repo/semantics/closedAccess
رقم الانضمام: edsbas.A1397FBB
قاعدة البيانات: BASE