Vitamin D and 1,25(OH)2D Regulation of T cells

被引:395
作者
Cantorna, Margherita T. [1 ,2 ]
Snyder, Lindsay [1 ]
Lin, Yang-Ding [1 ]
Yang, Linlin [1 ]
机构
[1] Penn State Univ, Dept Vet & Biomed Sci, University Pk, PA 16802 USA
[2] Penn State Univ, Ctr Mol Immunol & Infect Dis, University Pk, PA 16802 USA
关键词
D-RECEPTOR EXPRESSION; 1,25-DIHYDROXYVITAMIN D-3; NKT CELLS; IN-VIVO; ACTIVATION; IMMUNITY; IL-10; MICE; DIFFERENTIATION; PROLIFERATION;
D O I
10.3390/nu7043011
中图分类号
R15 [营养卫生、食品卫生]; TS201 [基础科学];
学科分类号
100403 ;
摘要
Vitamin D is a direct and indirect regulator of T cells. The mechanisms by which vitamin D directly regulates T cells are reviewed and new primary data on the effects of 1,25 dihydroxyvitamin D (1,25(OH)(2)D) on human invariant natural killer (iNK)T cells is presented. The in vivo effects of vitamin D on murine T cells include inhibition of T cell proliferation, inhibition of IFN-gamma, IL-17 and induction of IL-4. Experiments in mice demonstrate that the effectiveness of 1,25(OH)(2)D requires NKT cells, IL-10, the IL-10R and IL-4. Comparisons of mouse and human T cells show that 1,25(OH)(2)D inhibits IL-17 and IFN-gamma, and induces T regulatory cells and IL-4. IL-4 was induced by 1,25(OH)(2)D in mouse and human iNKT cells. Activation for 72h was required for optimal expression of the vitamin D receptor (VDR) in human and mouse T and iNKT cells. In addition, T cells are potential autocrine sources of 1,25(OH)(2)D but again only 48-72h after activation. Together the data support the late effects of vitamin D on diseases like inflammatory bowel disease and multiple sclerosis where reducing IL-17 and IFN-gamma, while inducing IL-4 and IL-10, would be beneficial.
引用
收藏
页码:3011 / 3021
页数:11
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