Teixeira Helena M P, Alcantara-Neves Neuza M, Barreto Maurício, Figueiredo Camila A, Costa Ryan S
Instituto de Ciências da Saúde, Universidade Federal da Bahia, Bahia, Brazil.
Instituto de Saúde Coletiva, Universidade Federal da Bahia, Bahia, Brazil.
Mol Immunol. 2017 Feb;82:137-145. doi: 10.1016/j.molimm.2017.01.001. Epub 2017 Jan 8.
Asthma is a chronic inflammatory disease of the respiratory tract. This heterogeneous disease is caused by the interaction of interindividual genetic variability and environmental factors. The gene adenylyl cyclase type 9 (ADCY9) encodes a protein called adenylyl cyclase (AC), responsible for producing the second messenger cyclic AMP (cAMP). cAMP is produced by T regulatory cells and is involved in the down-regulation of T effector cells. Failures in cAMP production may be related to an imbalance in the regulatory immune response, leading to immune-mediated diseases, such as allergic disorders. The aim of this study was to investigate how polymorphisms in the ADCY9 are associated with asthma and allergic markers. The study comprised 1309 subjects from the SCAALA (Social Changes Asthma and Allergy in Latin America) program. Genotyping was accomplished using the Illumina 2.5 Human Omni bead chip. Logistic regression was used to assess the association between allergy markers and ADCY9 variation in PLINK 1.07 software with adjustments for sex, age, helminth infection and ancestry markers. The ADCY9 candidate gene was associated with different phenotypes, such as asthma, specific IgE, skin prick test, and cytokine production. Among 133 markers analyzed, 29 SNPs where associated with asthma and allergic markers in silico analysis revealed the functional impact of the 6 SNPs on ADCY9 expression. It can be concluded that polymorphisms in the ADCY9 gene are significantly associated with asthma and/or allergy markers. We believe that such polymorphisms may lead to increased expression of adenylyl cyclase with a consequent increase in immunoregulatory activity. Therefore, these SNPs may offer an impact on the occurrence of these conditions in admixture population from countries such as Brazil.
哮喘是一种呼吸道慢性炎症性疾病。这种异质性疾病是由个体间基因变异性与环境因素相互作用引起的。9型腺苷酸环化酶(ADCY9)基因编码一种名为腺苷酸环化酶(AC)的蛋白质,负责产生第二信使环磷酸腺苷(cAMP)。cAMP由调节性T细胞产生,并参与效应T细胞的下调。cAMP产生缺陷可能与调节性免疫反应失衡有关,从而导致免疫介导的疾病,如过敏性疾病。本研究的目的是调查ADCY9基因多态性与哮喘及过敏标志物之间的关联。该研究纳入了来自拉丁美洲社会变化哮喘与过敏(SCAALA)项目的1309名受试者。基因分型使用Illumina 2.5人类全基因组珠芯片完成。在PLINK 1.07软件中采用逻辑回归评估过敏标志物与ADCY9变异之间的关联,并对性别、年龄、蠕虫感染和祖先标志物进行了校正。ADCY9候选基因与不同的表型相关,如哮喘、特异性IgE、皮肤点刺试验和细胞因子产生。在分析的133个标志物中,29个单核苷酸多态性(SNP)与哮喘和过敏标志物相关,计算机分析揭示了6个SNP对ADCY9表达的功能影响。可以得出结论,ADCY9基因多态性与哮喘和/或过敏标志物显著相关。我们认为,这种多态性可能导致腺苷酸环化酶表达增加,从而使免疫调节活性增强。因此,这些SNP可能对巴西等国混合人群中这些疾病的发生产生影响。