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尽管组织炎症受到抑制,但仍存在严重哮喘:U-BIOPRED 研究的结果。

Severe asthma exists despite suppressed tissue inflammation: findings of the U-BIOPRED study.

机构信息

Faculty of Medicine, University of Southampton and NIHR Respiratory Biomedical Research Unit, University of Southampton NHS Foundation Trust, Southampton, UK

Faculty of Medicine, University of Southampton and NIHR Respiratory Biomedical Research Unit, University of Southampton NHS Foundation Trust, Southampton, UK.

出版信息

Eur Respir J. 2016 Nov;48(5):1307-1319. doi: 10.1183/13993003.01129-2016. Epub 2016 Oct 6.

DOI:10.1183/13993003.01129-2016
PMID:27799384
Abstract

The U-BIOPRED study is a multicentre European study aimed at a better understanding of severe asthma. It included three steroid-treated adult asthma groups (severe nonsmokers (SAn group), severe current/ex-smokers (SAs/ex group) and those with mild-moderate disease (MMA group)) and healthy controls (HC group). The aim of this cross-sectional, bronchoscopy substudy was to compare bronchial immunopathology between these groups.In 158 participants, bronchial biopsies and bronchial epithelial brushings were collected for immunopathologic and transcriptomic analysis. Immunohistochemical analysis of glycol methacrylate resin-embedded biopsies showed there were more mast cells in submucosa of the HC group (33.6 mm) compared with both severe asthma groups (SAn: 17.4 mm, p<0.001; SAs/ex: 22.2 mm, p=0.01) and with the MMA group (21.2 mm, p=0.01). The number of CD4 lymphocytes was decreased in the SAs/ex group (4.7 mm) compared with the SAn (11.6 mm, p=0.002), MMA (10.1 mm, p=0.008) and HC (10.6 mm, p<0.001) groups. No other differences were observed.Affymetrix microarray analysis identified seven probe sets in the bronchial brushing samples that had a positive relationship with submucosal eosinophils. These mapped to COX-2 (cyclo-oxygenase-2), ADAM-7 (disintegrin and metalloproteinase domain-containing protein 7), SLCO1A2 (solute carrier organic anion transporter family member 1A2), TMEFF2 (transmembrane protein with epidermal growth factor like and two follistatin like domains 2) and TRPM-1 (transient receptor potential cation channel subfamily M member 1); the remaining two are unnamed.We conclude that in nonsmoking and smoking patients on currently recommended therapy, severe asthma exists despite suppressed tissue inflammation within the proximal airway wall.

摘要

U-BIOPRED 研究是一项多中心的欧洲研究,旨在更好地了解严重哮喘。它包括三组接受类固醇治疗的成年哮喘患者(严重非吸烟者(SAn 组)、严重现吸烟者/曾吸烟者(SAs/ex 组)和轻度至中度疾病患者(MMA 组))和健康对照组(HC 组)。本横断面支气管镜亚研究的目的是比较这些组之间的支气管免疫病理学。在 158 名参与者中,收集支气管活检和支气管上皮刷检进行免疫病理学和转录组学分析。糖甲氧基树脂包埋活检的免疫组织化学分析显示,与严重哮喘组(SAn:17.4mm,p<0.001;SAs/ex:22.2mm,p=0.01)和 MMA 组(21.2mm,p=0.01)相比,HC 组(33.6mm)的粘膜下肥大细胞更多。与 SAn 组(11.6mm,p=0.002)、MMA 组(10.1mm,p=0.008)和 HC 组(10.6mm,p<0.001)相比,SAs/ex 组的 CD4 淋巴细胞数量减少。Affymetrix 微阵列分析在支气管刷检样本中确定了七个与粘膜下嗜酸性粒细胞呈正相关的探针集。这些探针集映射到 COX-2(环氧化酶-2)、ADAM-7(解整合素和金属蛋白酶域蛋白 7)、SLCO1A2(溶质载体有机阴离子转运家族成员 1A2)、TMEFF2(跨膜蛋白与表皮生长因子样和两个卵泡抑素样结构域 2)和 TRPM-1(瞬时受体电位阳离子通道亚家族 M 成员 1);其余两个未命名。我们得出结论,在接受目前推荐治疗的非吸烟和吸烟患者中,尽管近端气道壁的组织炎症受到抑制,但仍存在严重哮喘。

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