Wang Shu-Chen, Chen Yi-Jing, Ou Tsan-Teng, Wu Cheng-Chin, Tsai Wen-Chan, Liu Hong-Wen, Yen Jeng-Hsien
Department of Laboratory Medicine, Kaohsiung Medical University Hospital, Kaohsiung, Taiwan.
J Clin Immunol. 2006 Nov;26(6):506-11. doi: 10.1007/s10875-006-9048-9. Epub 2006 Oct 6.
To investigate the role of programmed cell death-1 (PD-1) gene polymorphisms in the development of systemic lupus erythematosus (SLE) in Taiwan, 109 patients with SLE and 100 healthy controls were enrolled in this study. The PD-1 gene polymorphisms were determined by the method of polymerase chain reaction/restriction fragment length polymorphism. This study showed that the genotype distributions of PD-1 7209 C/T polymorphisms were significantly different between the patients with SLE and controls (P=0.002, Pc=0.018). The frequencies of the PD-1 7209 C/C genotype and PD-1 7209 C allele were significantly higher in the patients with SLE than those of the controls (P=0.001, OR=2.6, 95% CI=1.5-4.6, and P=0.002, OR=2.1, 95% CI=1.3-3.4, Pc=0.018, respectively). Moreover, the association of PD-1 7209 C with susceptibility to SLE was independent of the PD-1 ligand. This study also showed that the PD-1-536 A 7146 G 7209 C 7499 G haplotype was associated with the development of SLE in Taiwan.
为了研究程序性细胞死亡蛋白1(PD-1)基因多态性在台湾系统性红斑狼疮(SLE)发病中的作用,本研究纳入了109例SLE患者和100名健康对照。采用聚合酶链反应/限制性片段长度多态性方法检测PD-1基因多态性。本研究表明,SLE患者与对照组之间PD-1 7209 C/T多态性的基因型分布存在显著差异(P=0.002,Pc=0.018)。SLE患者中PD-1 7209 C/C基因型和PD-1 7209 C等位基因的频率显著高于对照组(分别为P=0.001,OR=2.6,95%CI=1.5-4.6;P=0.002,OR=2.1,95%CI=1.3-3.4,Pc=0.018)。此外,PD-1 7209 C与SLE易感性的关联独立于PD-1配体。本研究还表明,PD-1-536 A 7146 G 7209 C 7499 G单倍型与台湾SLE的发病有关。