Pégorier Sophie, Arouche Nassim, Dombret Marie-Christine, Aubier Michel, Pretolani Marina
Inserm U700, Paris, and Université Paris 7, Faculté de Médecine Denis Diderot, site Xavier Bichat, Paris, France.
J Allergy Clin Immunol. 2007 Dec;120(6):1301-7. doi: 10.1016/j.jaci.2007.09.023. Epub 2007 Nov 9.
Airway remodeling in patients with severe steroid-refractory asthma might result from a reduced ability of steroid therapy to limit the transcription of remodeling factors by the bronchial epithelium.
We sought to compare the levels of transcripts encoding remodeling factors in bronchial epithelium of healthy volunteers and of asthmatic patients with either steroid-sensitive or steroid-refractory disease and to correlate these levels with hallmarks of airway remodeling.
By means of real-time quantitative PCR, we assessed the levels of 14 transcripts encoding remodeling factors, matrix metalloproteinases, and extracellular matrix proteins in laser-capture microdissected bronchial epithelium of healthy volunteers, patients with mild steroid-untreated asthma, and patients with steroid-sensitive and steroid-refractory asthma (n = 8-10 in each group). Histologic features of airway remodeling and endothelin-1 (EDN1) immunolocalization were determined by using frozen specimens.
Patients with steroid-refractory asthma had greater levels of EDN1 transcripts (4.1-fold increase, P = .026) and protein (P = .0009) in their bronchial epithelium compared with patients with steroid-sensitive asthma. EDN1 mRNA levels and protein expression in asthmatic patients were negatively correlated with prebronchodilator and postbronchodilator FEV(1) value (r(2) >or= 0.193, P <or= .03), and they were positively related to airway smooth muscle areas (r(2) = 0.253, P = .01 and r(2) = 0.281, P = .005 for EDN1 mRNA and protein expression, respectively).
Increased EDN1 synthesis by the bronchial epithelium characterizes severe refractory asthma and correlates with airway remodeling and airflow obstruction.
Targeting EDN1 might represent a novel therapeutic strategy for severe steroid-refractory asthma.
重度激素抵抗型哮喘患者的气道重塑可能是由于激素疗法限制支气管上皮重塑因子转录的能力降低所致。
我们试图比较健康志愿者以及激素敏感型或激素抵抗型哮喘患者支气管上皮中编码重塑因子的转录本水平,并将这些水平与气道重塑的特征相关联。
通过实时定量聚合酶链反应,我们评估了健康志愿者、轻度未治疗哮喘患者、激素敏感型和激素抵抗型哮喘患者(每组8 - 10例)经激光捕获显微切割的支气管上皮中14种编码重塑因子、基质金属蛋白酶和细胞外基质蛋白的转录本水平。使用冷冻标本确定气道重塑的组织学特征和内皮素-1(EDN1)免疫定位。
与激素敏感型哮喘患者相比,激素抵抗型哮喘患者支气管上皮中的EDN1转录本水平(增加4.1倍,P = 0.026)和蛋白水平(P = 0.0009)更高。哮喘患者的EDN1 mRNA水平和蛋白表达与支气管扩张剂使用前和使用后的第一秒用力呼气容积(FEV₁)值呈负相关(r²≥0.193,P≤0.03),并且它们与气道平滑肌面积呈正相关(EDN1 mRNA和蛋白表达的r²分别为0.253,P = 0.01和r² = 0.281,P = 0.005)。
支气管上皮中EDN1合成增加是重度难治性哮喘的特征,并且与气道重塑和气流阻塞相关。
靶向EDN1可能是重度激素抵抗型哮喘的一种新型治疗策略。