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中国汉族人群中Toll样受体7和8基因多态性与哮喘及哮喘相关表型的关联

Associations of Toll-like receptor 7 and 8 Polymorphisms with Asthma and Asthma-related Phenotypes in a Chinese Han Population.

作者信息

Zhang Qian, Qian Fen-Hong, Yin Xiao-Wei, Cao Qi, Bai Jian-Ling, Du Qiang, Shi Yi

机构信息

Department of Respiratory Medicine, Affiliated Changzhou No.2 People's Hospital, Nanjing Medical University, Changzhou, China AND Department of Respiratory Medicine, Nanjing General Hospital of Nanjing Military Command, Nanjing, China.

Department of Respiratory Medicine, Affiliated Jiangbing Hospital, Jiangsu University, Zhenjiang, China.

出版信息

Iran J Allergy Asthma Immunol. 2015 Dec;14(6):569-80.

Abstract

Toll-like receptor (TLR) 7 and 8 mediate anti-virus immunity and are of particular relevance to asthma. However, very little information about genetic association on TLR7/8 and asthma are available. This study aimed to evaluate the effects of polymorphisms in TLR7 and 8 on asthma risk and asthma-related phenotypes in a Chinese Han population. We enrolled 462 unrelated adult asthmatic patients and 398 healthy volunteers. The genotypes of tagging single nucleotide polymorphisms (SNPs) in TLR7 and 8 genes were determined using multiplex SNaPshot SNP genotyping assay. We used case-control and case-only studies to assess any links with asthma and asthma-related phenotypes. There was no association between the variants in TLR7 and 8 and asthma susceptibility. However, our results revealed that the genetic variants in TLR7 and 8 were associated with asthma-related phenotypes, including eosinophil counts, serum immunoglobulin E levels, lung function, and asthma severity as well. Our study suggests that TLR7 and 8 polymorphisms may play a considerable role in the pathogenesis of asthma. It will help in better understanding the pathogenesis of asthma and development of more effective strategies for asthma prevention, prediction, and therapy.

摘要

Toll样受体(TLR)7和8介导抗病毒免疫,且与哮喘尤其相关。然而,关于TLR7/8与哮喘的基因关联的信息非常少。本研究旨在评估TLR7和8基因多态性对中国汉族人群哮喘风险及哮喘相关表型的影响。我们招募了462名无亲缘关系的成年哮喘患者和398名健康志愿者。使用多重SNaPshot SNP基因分型检测法确定TLR7和8基因中标签单核苷酸多态性(SNP)的基因型。我们采用病例对照研究和单纯病例研究来评估与哮喘及哮喘相关表型的任何关联。TLR7和8的变异与哮喘易感性之间无关联。然而,我们的结果显示TLR7和8的基因变异与哮喘相关表型有关,包括嗜酸性粒细胞计数、血清免疫球蛋白E水平、肺功能以及哮喘严重程度。我们的研究表明,TLR7和8基因多态性可能在哮喘发病机制中起重要作用。这将有助于更好地理解哮喘发病机制,并制定更有效的哮喘预防、预测和治疗策略。

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