Gene expression profile in multiple sclerosis patients and healthy controls:: identifying pathways relevant to disease

被引:163
作者
Bomprezzi, R
Ringnér, M
Kim, S
Bittner, ML
Khan, J
Chen, YD
Elkahloun, A
Yu, AM
Bielekova, B
Meltzer, PS
Martin, R
McFarland, HF
Trent, JM
机构
[1] NHGRI, Canc Genet Branch, NIH, Bethesda, MD 20892 USA
[2] Lund Univ, Dept Theoret Phys, SE-22362 Lund, Sweden
[3] Translat Genom Res Inst, Phoenix, AZ 85004 USA
[4] NCI, Ctr Adv Technol, NIH, Gaithersburg, MD 20877 USA
[5] NINDS, Neuroimmunol Branch, NIH, Bethesda, MD 20892 USA
关键词
D O I
10.1093/hmg/ddg221
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Multiple sclerosis (MS) and other T cell-mediated autoimmune diseases develop in individuals carrying a complex susceptibility trait, probably following exposure to various environmental triggers. Owing to the presumed weak influence of single genes on disease predisposition and the recognized genetic heterogeneity of autoimmune disorders in humans, candidate gene searches in MS have been difficult. In an attempt to identify molecular markers indicative of disease status rather than susceptibility genes for MS, we show that gene expression profiling of peripheral blood mononuclear cells by cDNA microarrays can distinguish MS patients from healthy controls. Our findings support the concept that the activation of autoreactive T cells is of primary importance for this complex organ-specific disorder and prompt further investigations on gene expression in peripheral blood cells aimed at characterizing disease phenotypes.
引用
收藏
页码:2191 / 2199
页数:9
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