Kaminska Marta, Foley Susan, Maghni Karim, Storness-Bliss Claudine, Coxson Harvey, Ghezzo Heberto, Lemière Catherine, Olivenstein Ronald, Ernst Pierre, Hamid Qutayba, Martin James
Meakins-Christie Laboratories, Montreal, Quebec H2X 2P2, Canada.
J Allergy Clin Immunol. 2009 Jul;124(1):45-51.e1-4. doi: 10.1016/j.jaci.2009.03.049. Epub 2009 May 29.
The patterns of airway remodeling and the biomarkers that distinguish different subtypes of severe asthma are unknown.
We sought to characterize subjects with severe asthma with and without chronic persistent airflow obstruction with respect to airway wall remodeling (histopathologic and radiologic) and specific sputum biomarkers.
Subjects with severe asthma with chronic persistent (n = 16) or intermittent (n = 18) obstruction were studied. Endobronchial biopsy specimens were analyzed for airway smooth muscle area, epithelial detachment, basement membrane thickness, and submucosal fibrosis. Levels of eosinophil cationic protein, myeloperoxidase, matrix metalloproteinase 9, tissue inhibitor of matrix metalloproteinase 1 (ELISA), and 27 cytokines (multiplex assay) and differential cell counts were measured in induced sputum. Airway thickness was measured by means of high-resolution computed tomographic scanning.
Chronic persistent obstruction was associated with earlier age of onset, longer disease duration, more inflammatory cells in the sputum, and greater smooth muscle area (15.65% +/- 2.69% [n = 10] vs 8.96% +/- 1.99% [n = 14], P = .0325). No differences between groups were found for any of the biomarker molecules measured in sputum individually. However, principal component analysis revealed that the dominant variables in the chronic persistent obstruction group were IL-12, IL-13, and IFN-gamma, whereas IL-9, IL-17, monocyte chemotactic protein 1, and RANTES were dominant in the other group. Airway imaging revealed no differences between groups.
Subjects with severe asthma with chronic persistent obstruction have increased airway smooth muscle with ongoing T(H)1 and T(H)2 inflammatory responses. Neither airway measurements on high-resolution computed tomographic scans nor sputum analysis seem able to identify such patients.
气道重塑模式以及区分重度哮喘不同亚型的生物标志物尚不清楚。
我们试图根据气道壁重塑(组织病理学和放射学)及特定痰液生物标志物,对有和无慢性持续性气流阻塞的重度哮喘患者进行特征描述。
研究了患有慢性持续性(n = 16)或间歇性(n = 18)阻塞的重度哮喘患者。对支气管活检标本进行气道平滑肌面积、上皮剥脱、基底膜厚度和黏膜下纤维化分析。在诱导痰中测量嗜酸性粒细胞阳离子蛋白、髓过氧化物酶、基质金属蛋白酶9、基质金属蛋白酶组织抑制剂1(酶联免疫吸附测定)水平以及27种细胞因子(多重检测)水平和细胞分类计数。通过高分辨率计算机断层扫描测量气道厚度。
慢性持续性阻塞与发病年龄较早、病程较长、痰液中炎症细胞较多以及平滑肌面积较大有关(15.65%±2.69% [n = 10] 对8.96%±1.99% [n = 14],P = .0325)。两组间在痰液中单独测量的任何生物标志物分子方面均未发现差异。然而,主成分分析显示,慢性持续性阻塞组的主要变量是白细胞介素-12、白细胞介素-13和干扰素-γ,而另一组中白细胞介素-9、白细胞介素-17、单核细胞趋化蛋白1和调节激活正常T细胞表达和分泌因子是主要变量。气道成像显示两组间无差异。
患有慢性持续性阻塞的重度哮喘患者气道平滑肌增加,伴有持续的辅助性T细胞1型和辅助性T细胞2型炎症反应。高分辨率计算机断层扫描气道测量和痰液分析似乎均无法识别此类患者。