Sakthivel Priya, Giscombe Ricardo, Ramanujam Ryan, Lefvert Ann Kari
Rheumatology Unit, Department of Medicine, Center for Molecular Medicine (L8:04), Karolinska Institutet, 17176, Stockholm, Sweden.
Rheumatol Int. 2009 Aug;29(10):1247-50. doi: 10.1007/s00296-009-0952-1. Epub 2009 May 18.
Genetic association of programmed cell death-1 (PDCD1) has been implicated in several autoimmune inflammatory disorders. Hence, in this study, our main objective is to evaluate the association of PDCD1 gene to Wegener's granulomatosis (WG). We, thus, analyzed three single nucleotide polymorphisms (SNPs) in PDCD1 gene among WG patients and controls. Further, we quantified circulating serum levels of soluble (s) PD-1 in patients and controls. The methodologies used were ABI Taqman allelic discrimination and restriction fragment length polymorphism for genotyping and in-house ELISA for quantifying sPD-1. Statistical relevance was analyzed by Fischer's exact test. As a result, reduced AA homozygote for SNP in intron-1 was observed, among the patients. However, no association was demonstrated after Bonferroni correction. Also, no differences in genotype and allele frequency were elucidated for SNPs in intron-4 and exon-5. Moreover, we could not demonstrate circulating sPD-1. In conclusion, we show no association of selected SNPs in PDCD1 gene with WG.
程序性细胞死亡蛋白1(PDCD1)的基因关联已涉及多种自身免疫性炎症性疾病。因此,在本研究中,我们的主要目的是评估PDCD1基因与韦格纳肉芽肿(WG)的关联。于是,我们分析了WG患者和对照组中PDCD1基因的三个单核苷酸多态性(SNP)。此外,我们对患者和对照组中可溶性(s)PD-1的循环血清水平进行了定量。所使用的方法是用于基因分型的ABI Taqman等位基因鉴别和限制性片段长度多态性以及用于定量sPD-1的内部ELISA。通过费舍尔精确检验分析统计学相关性。结果,在患者中观察到内含子1中SNP的AA纯合子减少。然而,经邦费罗尼校正后未显示出关联。此外,内含子4和外显子5中的SNP在基因型和等位基因频率上也没有差异。而且,我们未能检测到循环中的sPD-1。总之,我们发现PDCD1基因中选定的SNP与WG无关联。