Xu Qian, Tin Soe Kyaw, Sivalingam Suppiah Paramalingam, Thumboo Julian, Koh Dow Rhoon, Fong Kok Yong
Department of Medicine, National University of Singapore, Singapore.
Ann Acad Med Singap. 2007 Feb;36(2):91-5.
Interleukin-18 (IL-18) is a Th1 cytokine, which is postulated to play a role in systemic lupus erythematosus (SLE). Two single nucleotide polymorphisms (SNPs) in the IL-18 promoter gene region were found to influence the quantitative expression of the IL-18 protein. The aim of this study was to determine whether IL-18 promoter gene polymorphisms are associated with SLE.
One hundred and thirteen Chinese SLE patients and 218 Chinese healthy individuals were recruited. Genomic DNA was extracted from peripheral venous blood. Sequence-specific primer PCR and restriction fragment length polymorphism (RFLP) analysis were used to genotype the DNA samples for SNP-137 and SNP- 607. The following genotypes were obtained: SNP(-607) AA, AC, CC and SNP(-137) GG, GC, CC. Plasma IL-18 concentrations of patients and control subjects were measured by enzyme-linked immunosorbent assay.
the frequency of SNP-607/CC genotype was significantly higher in SLE patients (Pc < 0.05) while genotype SNP-607/AC was significantly decreased in SLE patients compared to the control group (Pc <0.05). Plasma IL-18 concentrations were significantly higher in SLE patients than in control subjects (P <0.05). Both patients and control subjects with CC and AC genotypes have significantly higher IL-18 concentrations than those with AA genotype.
The IL-18 promoter gene polymorphism SNP-607 C allele is associated with SLE and may result in the enhanced production of IL-18 protein in SLE and normal individuals.
白细胞介素-18(IL-18)是一种Th1细胞因子,据推测在系统性红斑狼疮(SLE)中发挥作用。已发现IL-18启动子基因区域的两个单核苷酸多态性(SNP)会影响IL-18蛋白的定量表达。本研究的目的是确定IL-18启动子基因多态性是否与SLE相关。
招募了113名中国SLE患者和218名中国健康个体。从外周静脉血中提取基因组DNA。采用序列特异性引物PCR和限制性片段长度多态性(RFLP)分析对DNA样本进行SNP-137和SNP-607基因分型。获得了以下基因型:SNP(-607)AA、AC、CC和SNP(-137)GG、GC、CC。通过酶联免疫吸附测定法测量患者和对照受试者的血浆IL-18浓度。
SLE患者中SNP-607/CC基因型的频率显著更高(Pc<0.05),而与对照组相比,SLE患者中SNP-607/AC基因型显著降低(Pc<0.05)。SLE患者的血浆IL-18浓度显著高于对照受试者(P<0.05)。CC和AC基因型的患者和对照受试者的IL-18浓度均显著高于AA基因型的患者和对照受试者。
IL-18启动子基因多态性SNP-607 C等位基因与SLE相关,可能导致SLE患者和正常个体中IL-18蛋白的产生增加。