免疫系统
免疫学
自身免疫
微阵列分析技术
微阵列
外周血单个核细胞
红斑狼疮
干扰素
系统性红斑狼疮
基因
生物
基因芯片分析
细胞因子
基因表达谱
DNA微阵列
基因表达
医学
抗体
遗传学
内科学
疾病
体外
作者
Mary K. Crow,Kyriakos A. Kirou,Jay G. Wohlgemuth
出处
期刊:Autoimmunity
[Informa]
日期:2003-12-01
卷期号:36 (8): 481-490
被引量:277
标识
DOI:10.1080/08916930310001625952
摘要
Altered regulation of interferon-α (IFNα) in systemic lupus erythematosus (SLE) was first demonstrated nearly 25 years ago. However, only recently has due attention been directed towards the central role of this cytokine family in SLE. Several laboratories have used large-scale microarray technology to study global gene expression patterns in heterogeneous populations of peripheral blood cells from lupus patients and control subjects. The results of these studies demonstrate that IFN-regulated genes are among the most significantly overexpressed in SLE mononuclear cells. In view of the protean effects of IFNs on immune system function, increased activity of IFNs may account for many of the immune system alterations that characterize SLE and contribute to autoimmunity. Definition of the nature of the major IFNs, or other factors, that drive the IFN-regulated gene expression signature noted in SLE is an important area for investigation that may lead to new approaches to targeted therapy of SLE.
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