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CTLA4 和 CD86 基因多态性与慢性阻塞性肺疾病易感性的关系。

CTLA4 and CD86 gene polymorphisms and susceptibility to chronic obstructive pulmonary disease.

机构信息

Department of Forensic Biology, West China School of Preclinical and Forensic Medicine, Sichuan University, Sichuan, China.

出版信息

Hum Immunol. 2010 Nov;71(11):1141-6. doi: 10.1016/j.humimm.2010.08.007. Epub 2010 Aug 21.

Abstract

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.

摘要

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。

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