Blood gene expression profiling in pediatric systemic lupus erythematosus and systemic juvenile idiopathic arthritis: from bench to bedside

被引:5
作者
Gilbert, Mileka [1 ]
Punaro, Marilynn [1 ]
机构
[1] Univ Texas SW Med Ctr Dallas, Childrens Med Ctr, Texas Scottish Rite Hosp Children, Dallas, TX 75390 USA
来源
PEDIATRIC RHEUMATOLOGY | 2014年 / 12卷
关键词
Gene expression profiling; DNA microarray; Interferon; Interleukin-1; Systemic lupus erythematosus; Systemic juvenile idiopathic arthritis; INTERLEUKIN-1 RECEPTOR ANTAGONIST; PLASMACYTOID DENDRITIC CELLS; AICARDI-GOUTIERES-SYNDROME; PLACEBO-CONTROLLED TRIAL; ACTIVATE B-CELLS; RHEUMATOID-ARTHRITIS; INTERFERON-ALPHA; I INTERFERON; DOUBLE-BLIND; IFN-ALPHA;
D O I
10.1186/1546-0096-12-16
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Blood gene expression profiling has led to major advances in the field of rheumatology over the last few decades. Specifically, DNA microarray technology has been integral in increasing our knowledge of key players in the pathogenesis of some rare pediatric rheumatic diseases. Our group, using microarray analysis, identified the interferon (IFN) gene signature in pediatric systemic lupus erythematosus (SLE) and has published data that suggest high doses of intravenous corticosteroid treatment may have benefit over strictly oral regimens. Additionally, DNA microarray technology led to our discovery that the interleukin (IL)-1 gene signature is associated with systemic juvenile idiopathic arthritis (sJIA) and to the use of IL-1 blockade with anakinra in this disease. We also reported the biologic rationale for use of anakinra early in the disease course. Anakinra is now being used as first-line treatment in sJIA in multiple centers. Herein, we review how information obtained from blood gene expression profiling has changed our clinical practice.
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页数:9
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