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Development, cytokine profile and function of human interleukin 17–producing helper T cells
被引:0
|作者:
Nicholas J Wilson
Katia Boniface
Jason R Chan
Brent S McKenzie
Wendy M Blumenschein
Jeanine D Mattson
Beth Basham
Kathleen Smith
Taiying Chen
Franck Morel
Jean-Claude Lecron
Robert A Kastelein
Daniel J Cua
Terrill K McClanahan
Edward P Bowman
Rene de Waal Malefyt
机构:
[1] Schering-Plough Biopharma (formerly DNAX Research),Department of Discovery Research
[2] Schering-Plough Biopharma (formerly DNAX Research),Department of Experimental Pathology and Pharmacology
[3] Laboratoire Cytokines et Inflammation EA 3806,undefined
[4] Universite de Poitiers,undefined
[5] Centre Hospitalier Universitaire de Poitiers,undefined
[6] Pole Biologie Sante,undefined
[7] Pineau,undefined
[8] Present address: Entelos,undefined
[9] Foster City,undefined
[10] California 94404,undefined
[11] USA.,undefined
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摘要:
TH-17 cells are a distinct lineage of proinflammatory T helper cells that are essential for autoimmune disease. In mice, commitment to the TH-17 lineage is dependent on transforming growth factor-β and interleukin 6 (IL-6). Here we demonstrate that IL-23 and IL-1β induced the development of human TH-17 cells expressing IL-17A, IL-17F, IL-22, IL-26, interferon-γ, the chemokine CCL20 and transcription factor RORγt. In situ, TH-17 cells were identified by expression of the IL-23 receptor and the memory T cell marker CD45RO. Psoriatic skin lesions contained IL-23-producing dendritic cells and were enriched in the cytokines produced by human TH-17 cells that promote the production of antimicrobial peptides in human keratinocytes. Our data collectively indicate that human and mouse TH-17 cells require distinct factors during differentiation and that human TH-17 cells may regulate innate immunity in epithelial cells.
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页码:950 / 957
页数:7
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