Institute for Lung Health, Department of Infection, Immunity and Inflammation, University of Leicester, Leicester, United Kingdom.
J Allergy Clin Immunol. 2010 Oct;126(4):722-729.e2. doi: 10.1016/j.jaci.2010.05.046. Epub 2010 Jul 31.
Epithelial dysfunction has been implicated in asthma pathophysiology, but no studies have directly assessed ciliary function in asthma.
To study the ciliary function and epithelial ultrastructure of patients with asthma and healthy controls.
We studied ciliary beat frequency and beat pattern by using digital high-speed video imaging and ultrastructure by transmission electron microscopy of bronchial epithelial strips from 7 subjects with mild, 7 with moderate, and 19 with severe asthma and 9 healthy controls.
The median (interquartile range) ciliary beat frequency was decreased in moderate (6.5 [4.4-8.5] Hz) and severe asthma (6.7 [6.1-7.6] Hz) compared with controls (10.5 [9.7-11.8] Hz; P < .01). Dyskinesia and immotility indices were higher in severe asthma (65% [43%-75%]; 6.3% [1%-9.5%], respectively) compared with controls (4% [0%-6.7%; 0%, respectively; P < .01). These abnormalities were related to disease severity (ciliary beat frequency, r(s) = -0.68; dyskinesia index, r(s) = 0.86; immotility index, r(s) = 0.65; P < .0001). The ultrastructure of the epithelium was abnormal in severe asthma with a reduction in ciliated cells, an increase in dead cells, and ciliary disorientation compared with all other groups (P < .05). Compared with patients with mild asthma and healthy controls, patients with severe asthma showed increased ciliary depletion, microtubular defects, mitochondrial damage, and cytoplasmic blebbing (P < .01). All of these changes were related to disease severity.
Ciliary dysfunction and ultrastructural abnormalities are closely related to asthma severity. Ciliary dysfunction is a feature of moderate to severe asthma, and profound ultrastructural abnormalities are restricted to severe disease. Whether these changes contribute to the development of severe asthma phenotype remains to be determined.
上皮功能障碍与哮喘病理生理学有关,但尚无研究直接评估哮喘患者的纤毛功能。
研究哮喘患者和健康对照者的纤毛功能和上皮超微结构。
我们使用数字高速视频成像研究了支气管上皮条带的纤毛摆动频率和摆动模式,并通过透射电子显微镜研究了超微结构,研究对象为 7 名轻度哮喘患者、7 名中度哮喘患者、19 名重度哮喘患者和 9 名健康对照者。
与对照组(10.5 [9.7-11.8] Hz)相比,中度(6.5 [4.4-8.5] Hz)和重度(6.7 [6.1-7.6] Hz)哮喘患者的中位(四分位距)纤毛摆动频率降低(P <.01)。重度哮喘患者的纤毛运动障碍指数(65% [43%-75%])和不动指数(6.3% [1%-9.5%])均高于对照组(4% [0%-6.7%]和 0%,分别;P <.01)。这些异常与疾病严重程度相关(纤毛摆动频率,rs = -0.68;纤毛运动障碍指数,rs = 0.86;不动指数,rs = 0.65;P <.0001)。与其他所有组相比,重度哮喘患者的上皮超微结构异常,表现为纤毛细胞减少、死细胞增加和纤毛方向紊乱(P <.05)。与轻度哮喘患者和健康对照者相比,重度哮喘患者的纤毛损耗、微管缺陷、线粒体损伤和细胞质泡状化增加(P <.01)。所有这些变化都与疾病严重程度相关。
纤毛功能障碍和超微结构异常与哮喘严重程度密切相关。纤毛功能障碍是中重度哮喘的特征,而严重的超微结构异常仅见于重度疾病。这些变化是否有助于严重哮喘表型的发展仍有待确定。