Dept of Respiratory Medicine, Academic Medical Center, Amsterdam, The Netherlands
Janssen R&D, Johnson & Johnson, Springhouse, PA, USA.
Eur Respir J. 2017 Sep 27;50(3). doi: 10.1183/13993003.02298-2016. Print 2017 Sep.
A proportion of severe asthma patients suffers from persistent airflow limitation (PAL), often associated with more symptoms and exacerbations. Little is known about the underlying mechanisms. Here, our aim was to discover unexplored potential mechanisms using Gene Set Variation Analysis (GSVA), a sensitive technique that can detect underlying pathways in heterogeneous samples.Severe asthma patients from the U-BIOPRED cohort with PAL (post-bronchodilator forced expiratory volume in 1 s/forced vital capacity ratio below the lower limit of normal) were compared with those without PAL. Gene expression was assessed on the total RNA of sputum cells, nasal brushings, and endobronchial brushings and biopsies. GSVA was applied to identify differentially enriched predefined gene signatures based on all available gene expression publications and data on airways disease.Differentially enriched gene signatures were identified in nasal brushings (n=1), sputum (n=9), bronchial brushings (n=1) and bronchial biopsies (n=4) that were associated with response to inhaled steroids, eosinophils, interleukin-13, interferon-α, specific CD4 T-cells and airway remodelling.PAL in severe asthma has distinguishable underlying gene networks that are associated with treatment, inflammatory pathways and airway remodelling. These findings point towards targets for the therapy of PAL in severe asthma.
一部分严重哮喘患者存在持续性气流受限(PAL),常伴有更多的症状和加重。目前对于其潜在机制知之甚少。在这里,我们使用基因集变异分析(GSVA)这一敏感技术,旨在发现潜在的、尚未探索的机制,以发现潜在的机制。该技术可以在异质样本中检测潜在的通路。
我们比较了 U-BIOPRED 队列中存在持续性气流受限(支气管扩张剂后 1 秒用力呼气容积/用力肺活量比值低于正常下限)的严重哮喘患者与不存在持续性气流受限的患者。通过痰细胞、鼻刷和支气管刷检及活检的总 RNA 评估基因表达。基于所有可用的基因表达出版物和气道疾病的数据,应用 GSVA 识别差异富集的预定义基因特征。
在鼻刷(n=1)、痰(n=9)、支气管刷检(n=1)和支气管活检(n=4)中鉴定到与吸入性皮质类固醇反应、嗜酸性粒细胞、白细胞介素 13、干扰素-α、特定 CD4 T 细胞和气道重塑相关的差异富集基因特征。
严重哮喘患者的 PAL 具有可区分的潜在基因网络,这些基因网络与治疗、炎症通路和气道重塑有关。这些发现为严重哮喘患者 PAL 的治疗提供了新的靶点。