Rus Violeta, Atamas Sergei P, Shustova Valentina, Luzina Irina G, Selaru Florin, Magder Laurence S, Via Charles S
Division of Rheumatology and Clinical Immunology, Department of Medicine, University of Maryland Medical School, Baltimore, Maryland 21201, USA.
Clin Immunol. 2002 Mar;102(3):283-90. doi: 10.1006/clim.2001.5182.
Systemic lupus erythematosus (SLE) is characterized by diverse and complex immune abnormalities. In an effort to begin to characterize the full complexity of immune abnormalities, the expression pattern of 375 potentially relevant genes was analyzed using peripheral blood mononuclear cells (PBMC) from 21 SLE patients and 12 controls by cDNA arrays. When mean gene expression for patients was compared to controls, 50 genes were identified that exhibited more than 2.5-fold difference in expression level. By the Mann-Whitney U test, 20 genes were significantly different (P < 0.05) between patients and controls. Most of these genes have not been previously associated with SLE and belong to a variety of families such as TNF/death receptor, IL-1 cytokine family, and IL-8 and its receptors. Hierarchical clustering of samples and differentially expressed genes revealed that with few exceptions, patients clustered separately from controls. These results highlight the potential use of the microarray data in identifying genes associated with SLE, which could become candidate molecular markers or future therapeutic targets.
系统性红斑狼疮(SLE)的特征是多样且复杂的免疫异常。为了开始全面描述免疫异常的复杂性,使用来自21例SLE患者和12例对照的外周血单个核细胞(PBMC),通过cDNA阵列分析了375个潜在相关基因的表达模式。将患者的平均基因表达与对照进行比较时,鉴定出50个基因,其表达水平差异超过2.5倍。通过Mann-Whitney U检验,患者和对照之间有20个基因存在显著差异(P < 0.05)。这些基因中的大多数以前未与SLE相关联,并且属于多种家族,如TNF/死亡受体、IL-1细胞因子家族以及IL-8及其受体。样本和差异表达基因的层次聚类显示,除了少数例外,患者与对照分别聚类。这些结果突出了微阵列数据在鉴定与SLE相关基因方面的潜在用途,这些基因可能成为候选分子标记或未来的治疗靶点。