Department of Forensic Biology, West China School of Preclinical and Forensic Medicine, Sichuan University, Sichuan, China.
Hum Immunol. 2010 Nov;71(11):1141-6. doi: 10.1016/j.humimm.2010.08.007. Epub 2010 Aug 21.
Chronic obstructive pulmonary disease (COPD) may be related to chronic inflammation and immune-mediated conditions, and its pathogenesis involves T-cell activation and proliferation. Cytotoxic T-lymphocyte-associated protein 4 (CTLA-4) and costimulatory molecules (CD80/CD86) genes are important mediators of T-cell activation in the immune response. The aim of this study was to investigate whether +2379G/C (rs17281995) and +1057G/A (rs1129055) in CD86 and -318C/T (rs5742909) and +49A/G (rs231775) in CTLA-4 genes single nucleotide polymorphisms (SNPs) are associated with COPD in a Chinese population. The four polymorphisms were identified in 396 COPD patients and 400 controls using polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP). The frequency of the T allele of the -318C/T in CTLA-4 and the A allele of the +1057G/A in CD86 polymorphisms showed significant association with COPD when compared with controls (T allele: p < 0.0001; A allele: p = 0.009). Comparison of genotype frequencies showed that -318CT, +1057GA, and +1057AA genotype was overrepresented in the COPD group, respectively (-318CT: 50.8% vs 28.5%, p < 0.0001; +1057GA: 58.6% vs 54.2%, p = 0.002; +1057AA: 30.1% vs 25.8%, p = 0.002). However, we failed to find any association between the four SNPs and COPD when cases were classified by smoking status or clinical stages (p > 0.05). The results indicate that the polymorphisms of CTLA-4 (-318C/T) and CD86 (+1057G/A) may be important genetic factor associated with risk or protection for COPD in Chinese population.
慢性阻塞性肺疾病(COPD)可能与慢性炎症和免疫介导的疾病有关,其发病机制涉及 T 细胞的激活和增殖。细胞毒性 T 淋巴细胞相关蛋白 4(CTLA-4)和共刺激分子(CD80/CD86)基因是免疫反应中 T 细胞激活的重要介质。本研究旨在探讨 CD86 基因中的+2379G/C(rs17281995)和+1057G/A(rs1129055)以及 CTLA-4 基因中的-318C/T(rs5742909)和+49A/G(rs231775)单核苷酸多态性(SNP)是否与中国人群中的 COPD 相关。采用聚合酶链反应-限制性片段长度多态性(PCR-RFLP)法检测 396 例 COPD 患者和 400 例对照者 CD86 基因中的 4 个 SNP。与对照组相比,CTLA-4 基因中的-318C/T 多态性的 T 等位基因和 CD86 基因中的+1057G/A 多态性的 A 等位基因频率与 COPD 显著相关(T 等位基因:p<0.0001;A 等位基因:p=0.009)。基因型频率比较显示,COPD 组中-318CT、+1057GA 和+1057AA 基因型频率升高(-318CT:50.8%比 28.5%,p<0.0001;+1057GA:58.6%比 54.2%,p=0.002;+1057AA:30.1%比 25.8%,p=0.002)。然而,当根据吸烟状况或临床分期对病例进行分类时,我们未能发现这 4 个 SNP 与 COPD 之间存在任何关联(p>0.05)。结果表明,CTLA-4(-318C/T)和 CD86(+1057G/A)多态性可能是中国人群 COPD 发生风险或保护的重要遗传因素。