Centre for Heart and Lung Innovation, St. Paul's Hospital, University of British Columbia, Vancouver, BC, Canada
Dept of Respiratory Medicine, Graduate School of Medicine, Kyoto University, Kyoto, Japan.
Eur Respir J. 2018 Feb 14;51(2). doi: 10.1183/13993003.01245-2017. Print 2018 Feb.
The small conducting airways are the major site of obstruction in chronic obstructive pulmonary disease (COPD). This study examined small airway pathology using a novel combination of multidetector row computed tomography (MDCT), micro-computed tomography (microCT) and histology.Airway branches visible on specimen MDCT were counted and the dimensions of the third- to fifth-generation airways were computed, while the terminal bronchioles (designated TB), preterminal bronchioles (TB-1) and pre-preterminal bronchioles (TB-2) were examined with microCT and histology in eight explanted lungs with end-stage COPD and seven unused donor lungs that served as controls.On MDCT, COPD lungs showed a decrease in the number of 2-2.5 mm diameter airways and the lumen area of fifth-generation airways, while on microCT there was a reduction in the number of terminal bronchioles as well as a decrease in the luminal areas, wall volumes and alveolar attachments to the walls of TB, TB-1 and TB-2 bronchioles. The combination of microCT and histology showed increased B-cell infiltration into the walls of TB-1 and TB-2 bronchioles, and this change was correlated with a reduced number of alveolar attachments in COPD.Small airways disease extends from 2 mm diameter airways to the terminal bronchioles in COPD. Destruction of alveolar attachments may be driven by a B-cell-mediated immune response in the preterminal bronchioles.
小气道是慢性阻塞性肺疾病(COPD)的主要阻塞部位。本研究使用多排螺旋 CT(MDCT)、微计算机断层扫描(microCT)和组织学的新组合来检查小气道病理学。在标本 MDCT 上可见的气道分支进行计数,并计算第三至第五代气道的尺寸,而用 microCT 和组织学检查在八个终末期 COPD 离体肺和七个未使用的供体肺中检查末端细支气管(TB)、前末端细支气管(TB-1)和前前末端细支气管(TB-2)。在 MDCT 上,COPD 肺显示 2-2.5mm 直径气道数量和第五代气道管腔面积减少,而在 microCT 上,末端细支气管数量减少,管腔面积、壁体积和肺泡与 TB、TB-1 和 TB-2 细支气管壁的附着减少。microCT 和组织学的组合显示 B 细胞浸润到 TB-1 和 TB-2 细支气管壁增加,这种变化与 COPD 中肺泡附着减少相关。小气道疾病从小气道直径 2mm 延伸到末端细支气管。终末细支气管的肺泡附着破坏可能是由前末端细支气管中的 B 细胞介导的免疫反应驱动的。