Comparative effect of 25(OH)D3 and 1,25(OH)2D3 on Th17 cell differentiation

被引:44
作者
Fawaz, Lama [1 ]
Mrad, May F. [2 ]
Kazan, Jalal M. [2 ]
Sayegh, Souraya [1 ]
Akika, Reem [1 ]
Khoury, Samia J. [2 ]
机构
[1] Amer Univ Beirut, Fac Med, Dept Expt Pathol Microbiol & Immunol, POB 11-0236, Beirut, Lebanon
[2] Amer Univ Beirut, Med Ctr, Nehme & Therese Tohme Multiple Sclerosis Ctr, Abu Haidar Neurosci Inst,Fac Med, Beirut, Lebanon
关键词
Th17; Vitamin D; IL-17A; HUMAN PERIPHERAL-BLOOD; VITAMIN-D; T-CELLS; 25-HYDROXYVITAMIN D-3; AUTOIMMUNE INFLAMMATION; CROHNS-DISEASE; RECEPTOR; ACTIVATION; RESPONSES; DRIVES;
D O I
10.1016/j.clim.2016.02.011
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Vitamin D is a secosteroid hormone that plays an important regulatory role in calcium homeostasis and bone metabolism. Immune cells can both produce and respond to 1,25(OH)(2)D3. CD4+ T cells from vitamin D receptor (VDR) KO mice produce higher levels of IFN-gamma and IL-17 than their wild type counterparts, and play a crucial role in the pathogenesis of autoimmune diseases (AID). We are particularly interested in studying the effect of vitamin D on pathogenic Th17 cells in humans. We investigated the in vitro effect of 1,25(OH)(2)D3 and 25(OH)D3 on the differentiation and cytokine production of primary CD4+ T cells from normal donors, and cultured in Th17 polarizing conditions. Both forms of vitamin D reduced the expression of pathogenic Th17 markers and their secretion of pro-inflammatory cytokines (IL-17A, IFN-gamma). Furthermore, both vitamin D forms induced an expansion of CD25hi cells and upregulated their expression of CTLA-4 and Foxp3 regulatory markers. (C) 2016 Elsevier Inc. All rights reserved.
引用
收藏
页码:59 / 71
页数:13
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