Brown J R, Kleimberg J, Marini M, Sun G, Bellini A, Mattoli S
Diagnostic Centre for Respiratory and Allergic Diseases, Institute of Experimental Medicine, Milano, Italy.
Clin Exp Immunol. 1998 Nov;114(2):137-46. doi: 10.1046/j.1365-2249.1998.00688.x.
We investigated the kinetics of allergen-induced eotaxin expression and its relationship to eosinophil accumulation and activation in the airways of patients with allergic asthma. Twenty-four patients with allergic asthma and late asthmatic responses to allergen inhalation were randomly allocated into three groups of eight patients each, who received bronchoscopy with bronchial biopsies and BAL at 2, 4 and 24 h, respectively, after the inhalation of the diluent and the allergen. The expression of eotaxin mRNA and protein and eotaxin release were evaluated by in situ hybridization, immunohistochemistry, immunocytochemistry, and radioimmunoassay. Increased transcription from the eotaxin gene preceded the appearance of the late asthmatic response and the influx of activated eosinophils in bronchial tissue and BAL fluid (BALF). This was followed by increased cell expression of eotaxin protein (P<0.001) and increased eotaxin release (P<0.001), which correlated with the numbers of total and activated eosinophils and the level of airflow obstruction at 4 h after allergen exposure (P<0.05 for all correlations). At 24 h after allergen inhalation, enhanced eotaxin expression declined without a similar reduction in the numbers of eosinophils in bronchial biopsies and when there was a further increase in the number of these cells in BALF (P<0.05). These results indicate that eotaxin contributes to the early phase of allergen-induced recruitment of activated eosinophils into the airways of patients with allergic asthma and that other factors are implicated in the persistence of eosinophil infiltration.
我们研究了变应原诱导的嗜酸性粒细胞趋化因子表达动力学及其与过敏性哮喘患者气道中嗜酸性粒细胞积聚和活化的关系。24例对变应原吸入有迟发性哮喘反应的过敏性哮喘患者被随机分为三组,每组8例,分别在吸入稀释剂和变应原后2小时、4小时和24小时接受支气管镜检查并进行支气管活检和支气管肺泡灌洗(BAL)。通过原位杂交、免疫组织化学、免疫细胞化学和放射免疫测定法评估嗜酸性粒细胞趋化因子mRNA和蛋白的表达以及嗜酸性粒细胞趋化因子的释放。嗜酸性粒细胞趋化因子基因转录增加先于迟发性哮喘反应的出现以及支气管组织和支气管肺泡灌洗液(BALF)中活化嗜酸性粒细胞的流入。随后嗜酸性粒细胞趋化因子蛋白的细胞表达增加(P<0.001)以及嗜酸性粒细胞趋化因子释放增加(P<0.001),这与变应原暴露后4小时的总嗜酸性粒细胞和活化嗜酸性粒细胞数量以及气流阻塞水平相关(所有相关性P<0.05)。在变应原吸入后24小时,增强的嗜酸性粒细胞趋化因子表达下降,但支气管活检中嗜酸性粒细胞数量没有类似减少,而BALF中这些细胞数量进一步增加(P<0.05)。这些结果表明,嗜酸性粒细胞趋化因子有助于变应原诱导的活化嗜酸性粒细胞早期募集到过敏性哮喘患者的气道中,并且其他因素与嗜酸性粒细胞浸润的持续存在有关。