Effects of vitamin D on expression of Toll-like receptors of monocytes from patients with Behcet's disease

被引:125
作者
Do, J. E. [1 ]
Kwon, S. Y. [1 ]
Park, S. [2 ]
Lee, E. -S. [1 ]
机构
[1] Ajou Univ, Sch Med, Dept Dermatol, Suwon 443721, South Korea
[2] Ajou Univ, Sch Med, Dept Microbiol, Suwon 443721, South Korea
关键词
Behcet's disease; monocyte; toll-like receptors; vitamin D;
D O I
10.1093/rheumatology/ken109
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objectives. Recent studies have shown the immunomodulatory effect of vitamin D-3 through down-regulation of Toll-like receptor (TLR) expression in human monocytes. To understand the implication of innate immunity with the role of vitamin D affecting TLR expression in Behcet's disease (BD), we focused on the association between the TLR expression and the serum vitamin D concentration in BD. Methods. The expression of TLR2, TLR4 and CD16 on monocytes was detected by flow cytometric analysis and RT-PCR. Serum 25-hydroxyvitamin D [25(OH)D] levels were measured in the patients with BD, psoriasis and healthy controls, and then the expression of TLRs was correlated with the value of serum 25(OH)D levels. To assess the influence of vitamin D3 on expression and function of TLRs in vitro, human monocytes were treated with increasing concentrations of 1,25(OH)(2)D-3. Results. We found that the monocytes of active BD patients showed higher expressions of TLR2 and TLR4 than those of controls, and serum 25(OH)D levels tended to be lower in active BD. Furthermore, 25(OH) D levels were inversely correlated with the expressions of TLR2, TLR4 and clinical indicators. In vitro analysis showed that vitamin D-3 was found to dose-dependently suppress the protein and mRNA expressions of TLR2 and TLR4. TNF-alpha synthesis was also decreased upon TLR ligand stimulation in vitamin D-3-treated monocytes. Conclusion. These results suggest that the inflammation triggered through TLR2 and TLR4 is important in the pathogenesis of BD. And it seems possible that vitamin D may be used as a therapeutic option by modulating TLR2 and TLR4 expression of monocytes in BD.
引用
收藏
页码:840 / 848
页数:9
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