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Disparate distribution of activating and inhibitory killer cell immunoglobulin-like receptor genes in patients with systemic lupus erythematosus.

机译:系统性红斑狼疮患者中活化和抑制性杀伤细胞免疫球蛋白样受体基因的分布不同。

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The genes of killer cell immunoglobulin-like receptors (KIRs), which are involved in the activation of T cells and natural killer cells, are highly variable. In recent years, the role of KIRs in autoimmune diseases has received increasing attention. The present study was undertaken to determine the association of the polymorphism of KIR genes with the susceptibility to systemic lupus erythematosus (SLE). The polymorphism of KIR genes of 93 patients with SLE together with 123 healthy donors as the control group was determined by polymerase chain reaction with sequence-specific primers. Twenty-seven novel gene combinations were found. Genotypic frequencies of KIR2DL2 (p < 0.001) and KIR2DS1 (p < 0.001) were much higher in patients with SLE than in control subjects. Individuals with two and more than two activating KIR genes were found more frequently in patients than in control subjects (80.7% versus 66.7%, p = 0.022). The results suggest that a genetic disturbance between activating and inhibitory KIR genes may be one of the key factors underlying the pathogenesis of SLE.
机译:参与T细胞和自然杀伤细胞激活的杀伤细胞免疫球蛋白样受体(KIR)基因高度可变。近年来,KIR在自身免疫性疾病中的作用日益受到关注。本研究旨在确定KIR基因多态性与对系统性红斑狼疮(SLE)的敏感性之间的关系。通过聚合酶链反应与序列特异性引物确定93例SLE患者和123例健康供者的KIR基因多态性。发现了二十七个新基因组合。 SLE患者的KIR2DL2(p <0.001)和KIR2DS1(p <0.001)的基因型频率比对照组高得多。与对照组相比,患者中具有两个和两个以上激活KIR基因的个体发生率更高(80.7%对66.7%,p = 0.022)。结果表明,激活和抑制性KIR基因之间的遗传干扰可能是SLE发病机理的关键因素之一。

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