CIBER Enfermedades Respiratorias, Barcelona, Spain.
Institut de Recerca Biomedica August Pi i Sunyer (IDIBAPS), Barcelona, Spain.
Respir Res. 2019 Jul 12;20(1):152. doi: 10.1186/s12931-019-1105-z.
Chronic Obstructive Pulmonary Disease (COPD) is associated with an abnormal pulmonary and systemic immune response to tobacco smoking. Yet, how do immune cells relate within and between these two biological compartments, how the pulmonary infiltrate influences the lung transcriptome, and what is the role of active smoking vs. presence of disease is unclear.
To investigate these questions, we simultaneously collected lung tissue and blood from 65 individuals stratified by smoking habit and presence of the disease. The immune cell composition of both tissues was assessed by flow cytometry, whole lung transcriptome was determined with Affymetrix arrays, and we used Weighted Gene Co-expression Network Analysis (WGCNA) to integrate results.
Main results showed that: (1) current smoking and the presence of COPD were both independently associated with a reduction in the proportion of lung T cells and an increase of macrophages, specifically those expressing CD80 + CD163+; (2) changes in the proportion of infiltrating macrophages, smoking status or the level of airflow limitation were associated to different WGCNA modules, which were enriched in iron ion transport, extracellular matrix and cilium organization gene ontologies; and, (3) circulating white blood cells counts were correlated with lung macrophages and T cells.
Mild-moderated COPD lung immune infiltrate is associated with the active smoking status and presence of disease; is associated with changes in whole lung tissue transcriptome and marginally reflected in blood.
慢性阻塞性肺疾病(COPD)与对烟草烟雾的异常肺和系统免疫反应有关。然而,免疫细胞在这两个生物隔室中如何相互关联,肺部浸润如何影响肺转录组,以及主动吸烟与疾病存在的作用如何尚不清楚。
为了研究这些问题,我们同时从 65 名按吸烟习惯和疾病存在分层的个体中收集肺组织和血液。通过流式细胞术评估两种组织的免疫细胞组成,用 Affymetrix 阵列确定全肺转录组,并使用加权基因共表达网络分析(WGCNA)来整合结果。
主要结果表明:(1)当前吸烟和 COPD 的存在均与肺 T 细胞比例降低和巨噬细胞增加独立相关,特别是表达 CD80+CD163+的巨噬细胞;(2)浸润性巨噬细胞比例、吸烟状况或气流受限程度的变化与不同的 WGCNA 模块相关,这些模块富含铁离子转运、细胞外基质和纤毛组织的基因本体论;(3)循环白细胞计数与肺巨噬细胞和 T 细胞相关。
轻度至中度 COPD 肺部免疫浸润与主动吸烟状况和疾病存在有关;与整个肺组织转录组的变化有关,在血液中略有反映。