University of Manchester, Medicines Evaluation Unit, University Hospital of South Manchester Foundation Trust, Manchester M23 9LT, UK.
Thorax. 2011 Jun;66(6):489-95. doi: 10.1136/thx.2010.153767. Epub 2011 Mar 24.
Induced sputum is used to sample inflammatory cells, predominantly neutrophils and macrophages, from the airways of COPD patients. The author's aim was to identify candidate genes associated with the degree of airflow obstruction and the extent of emphysema by expression profiling, and then to confirm these findings for selected candidates using PCR and protein analysis.
Two sputum studies were performed in Global Initiative for Chronic Obstructive Lung Disease (GOLD) stage 2-4 COPD ex-smokers from the Evaluation of COPD Longitudinally to Identify Predictive Surrogate Endpoints (ECLIPSE) cohort. First, gene array profiling at baseline in samples from 148 patients. The findings were replicated in a separate population of 176 patients using real-time PCR. The findings for one selected gene IL-18R were further analysed using immunohistochemistry in lung tissue and induced sputum from patients outside the ECLIPSE cohort.
Gene expression profiling revealed changes in 277 genes associated with GOLD stage 2 versus 3 and 4, and 198 genes with changes associated with the degree of emphysema (p < 0.01 for each gene). Twelve of these candidate genes were analysed by PCR in the replication cohort, with significant changes (p < 0.05) observed for 11 genes. IL-18R protein expression was higher on alveolar macrophages in lung tissue of COPD patients (mean 23.2%) compared to controls (mean ex-smokers 2% and non-smokers 2.5%).
Gene expression profiling in sputum cells identified candidate genes that may play roles in molecular mechanisms associated with COPD. The replication by PCR and protein in different studies confirms these findings, and highlights a potential role for IL-18R upregulation in severe COPD.
诱导痰用于从 COPD 患者的气道中采样炎症细胞,主要是中性粒细胞和巨噬细胞。作者的目的是通过表达谱鉴定与气流阻塞程度和肺气肿程度相关的候选基因,然后使用 PCR 和蛋白质分析对选定的候选基因进行验证。
在来自慢性阻塞性肺疾病纵向评估以确定预测替代终点(ECLIPSE)队列的 GOLD 2-4 期 COPD 戒烟者的 2 项痰研究中进行。首先,在 148 例患者的基线样本中进行基因芯片分析。使用实时 PCR 在另一个 176 例患者的人群中复制了这些发现。对一个选定基因 IL-18R 的发现使用肺组织和来自 ECLIPSE 队列之外的患者的诱导痰进行免疫组织化学进一步分析。
基因表达谱分析显示,与 GOLD 2 期与 3 期和 4 期相比,277 个基因发生变化,与肺气肿程度相关的 198 个基因发生变化(每个基因的 p <0.01)。在复制队列中分析了这 12 个候选基因中的 11 个基因的 PCR,观察到 11 个基因的显著变化(p <0.05)。与对照组(平均戒烟者 2%和非吸烟者 2.5%)相比,COPD 患者肺组织中的肺泡巨噬细胞中 IL-18R 蛋白表达更高(平均 23.2%)。
痰细胞中的基因表达谱分析确定了可能在与 COPD 相关的分子机制中起作用的候选基因。PCR 和蛋白质在不同研究中的复制证实了这些发现,并强调了 IL-18R 上调在严重 COPD 中的潜在作用。