Effect of Infliximab on Gene Expression Profiling in Behcet's Disease

被引:20
作者
Keino, Hiroshi [1 ]
Watanabe, Takayo [1 ]
Taki, Wakako [1 ]
Okada, Annabelle A. [1 ]
机构
[1] Kyorin Univ, Sch Med, Dept Ophthalmol, Tokyo 1818611, Japan
关键词
TUMOR-NECROSIS-FACTOR; REGULATORY T-CELLS; RHEUMATOID-ARTHRITIS; IN-VIVO; UVEITIS; CYCLOSPORINE; TUBERCULOSIS; ASSOCIATION; RECEPTOR-4; ANTIBODIES;
D O I
10.1167/iovs.11-7999
中图分类号
R77 [眼科学];
学科分类号
100212 ;
摘要
PURPOSE. Recent studies have demonstrated that a new antitumor necrosis factor (TNF)-alpha antibody, infliximab, is effective in controlling ocular inflammatory attacks in Behcet's disease. In this study, the effect of infliximab on gene expression patterns in peripheral blood mononuclear cells of Behcet's disease patients was investigated before and after initiation of infliximab treatment. METHODS. A human whole-genome microarray of 54,359 genes was used to analyze mRNA expression profiles of peripheral blood mononuclear cells obtained from four patients (three women, one man, 21-64 years at age) at baseline and at 22 weeks after initiation of infliximab. Quantitative polymerase chain reaction (PCR) analysis was performed for selected up -or downregulated genes, to confirm the microarray results. RESULTS. Anti-TNF-alpha therapy reduced the frequency of ocular episodes in three of four patients. Among inflammatory cytokine-related genes, TNF blockade reduced expression of interleukin (IL)-1 receptor type 2, interferon-gamma receptors, IL6, IL6 receptor, gp130, and IL17 receptors. Furthermore, gene expression of Toll-like receptor 2 (TLR2), receptor for mycobacterial glycolipid (C-type lectin domain family 4, member E: CLEC4E), and complexin 2 (CPLX2)was downregulated in all patients. CONCLUSIONS. Several up- or downregulated genes identified in this study may be candidates for further investigation in identifying the molecular mechanism of infliximab in the treatment of Behcet's disease with refractory uveoretinitis. (Invest Ophthalmol Vis Sci. 2011;52:7681-7686) DOI:10.1167/iovs.11-7999
引用
收藏
页码:7681 / 7686
页数:6
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