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Peripheral blood gene expression changes during allergen inhalation challenge in atopic asthmatic individuals

机译:过敏性哮喘个体吸入变应原过程中外周血基因表达的变化

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Objectives. (1) To investigate the effects of globin mRNA depletion in detecting differential gene expression in peripheral blood and (2) to investigate changes in peripheral blood gene expression in atopic asthmatic individuals undergoing allergen inhalation challenge. Methods. Asthmatic subjects (2060 years of age, with stable, mild allergic asthma, n = 9) underwent allergen inhalation challenges. All had an early asthmatic response of ≥20% fall in forced expiratory volume in 1 second. Blood was collected immediately prior to and 2 hours after allergen challenge using PAXgene tubes (n = 4) and EDTA tubes (n = 5). Aliquots of the PAXgene blood samples were subjected to globin reduction (PAX-GR). Transcriptome analysis was performed using Affymetrix GeneChip? Human Gene 1.0 ST arrays. Data were preprocessed using factor analysis for robust microarray summarization and analyzed using linear models for microarrays. Pathway analyses were performed using Ingenuity Pathway Analysis. Results. Globin reduction uncovered probe sets of lower abundance. However, it significantly reduced the ability to detect differentially expressed genes (DEGs) when compared to non-globin-reduced PAXgene samples (PAX-NGR). Combined transcriptional analysis of four PAX-NGR and five EDTA sample pairs identified 1595 DEGs associated with allergen inhalation challenge (false discovery rate ≤ 5%), with the top-ranked network of perturbed biological functions consisting of inflammatory response, cellular movement, and immune cell trafficking. Conclusions. While we have demonstrated a diminished ability to detect DEGs after globin reduction, we have nevertheless identified significant changes in the peripheral blood transcriptome of people with mild asthma 2 hours after allergen inhalation challenge.
机译:目标。 (1)研究球蛋白mRNA耗竭对检测外周血中差异基因表达的影响,以及(2)研究经历过敏原吸入攻击的特应性哮喘患者外周血基因表达的变化。方法。哮喘受试者(2060岁,患有稳定,轻度过敏性哮喘,n = 9)经历了过敏原吸入挑战。所有人的早期哮喘反应在1秒内强迫呼气量下降≥20%。使用PAXgene管(n = 4)和EDTA管(n = 5)立即在变应原攻击之前和之后2小时收集血液。将PAXgene血液样本的等分试样进行球蛋白还原(PAX-GR)。使用Affymetrix GeneChip?进行转录组分析。人类基因1.0 ST阵列。使用因子分析对数据进行预处理,以实现可靠的微阵列汇总,并使用线性模型对微阵列进行分析。路径分析是使用Ingenuity Pathway Analysis进行的。结果。球蛋白还原发现较低丰度的探针组。但是,与非球蛋白还原的PAXgene样品(PAX-NGR)相比,它显着降低了检测差异表达基因(DEG)的能力。结合对四个PAX-NGR和五个EDTA样品对的转录分析,确定了1595个与过敏原吸入挑战相关的DEG(错误发现率≤5%),其顶级的扰动生物学功能网络包括炎症反应,细胞运动和免疫细胞运输。结论。尽管我们已经证明减少球蛋白后检测DEG的能力降低了,但是我们已经发现,在过敏原吸入后2小时,轻度哮喘患者的外周血转录组显着变化。

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