Tian Xinrui, Tian Xinli, Huo Rujie, Chang Qin, Zheng Guoping, Du Yan, Chen Yan, Niu Bo
a Department of Respiratory Medicine , The Second Hospital of Shanxi Medical University , Taiyuan , China.
b Heart and Lung Center, Chinese PLA General Hospital of Beijing Military Region , Beijing , China.
Hum Vaccin Immunother. 2017 Aug 3;13(8):1758-1764. doi: 10.1080/21645515.2017.1313366. Epub 2017 Apr 25.
Bacillus Calmette-Guerin (BCG) is a potent agent for the prevention of tuberculosis. Current studies have regarded BCG as an immunomodulator. However, there is little information on whether it can be used to inhibit airway inflammation and airway remodeling caused by asthma. Therefore, in this study, we investigate the role of epithelial-mesenchymal transition (EMT) in airway inflammation and airway remodeling as well as the possible therapeutic mechanism of BCG for the treatment of asthma. Wistar rats were sensitized and challenged by ovalbumin for 2 weeks or 8 weeks. BCG was subcutaneously administered daily before every ovalbumin challenge to determine its therapeutic effects. The 2 weeks model group showed extensive eosinophilia, chronic inflammatory responses, bronchial wall thickening, airway epithelium damage, increased levels of transforming growth factor β 1 (TGF-β) in both bronchoalveolar lavage fluid and sera, decreased expression of epithelial marker E-cadherin, and increased expressions of mesenchymal markers α-smooth muscle actin (α-SMA) and Fibronectin (Fn). Except for inflammatory responses, all responses were more significant in the 8 weeks model group which displayed characteristics of airway remodeling including subepithelial fibrosis, smooth muscle hypertrophy, and goblet cell hyperplasia. When compared with the model groups, BCG administration inhibited airway inflammation and airway remodeling, decreased TGF-β levels, upregulated expression of E-cadherin, and downregulated expression of α-SMA and Fn. The present study suggests for the first time that increased secretion of TGF- β induced by asthmatic chronic inflammation may result in EMT, which is one of the most important mechanisms of airway inflammation and airway remodeling seen with asthma. BCG alleviates airway inflammation and airway remodeling by preventing TGF-β induced EMT, therefore BCG may be a new therapy for treating asthma.
卡介苗(BCG)是预防结核病的一种有效制剂。目前的研究已将卡介苗视为一种免疫调节剂。然而,关于它是否可用于抑制哮喘引起的气道炎症和气道重塑,相关信息甚少。因此,在本研究中,我们探究了上皮-间质转化(EMT)在气道炎症和气道重塑中的作用以及卡介苗治疗哮喘的可能机制。将Wistar大鼠用卵清蛋白致敏并激发2周或8周。在每次卵清蛋白激发前每日皮下注射卡介苗以确定其治疗效果。2周模型组表现出广泛的嗜酸性粒细胞增多、慢性炎症反应、支气管壁增厚、气道上皮损伤、支气管肺泡灌洗液和血清中转化生长因子β1(TGF-β)水平升高、上皮标志物E-钙黏蛋白表达降低以及间充质标志物α-平滑肌肌动蛋白(α-SMA)和纤连蛋白(Fn)表达增加。除炎症反应外,所有这些反应在8周模型组中更为显著,该组表现出气道重塑的特征,包括上皮下纤维化、平滑肌肥大和杯状细胞增生。与模型组相比,给予卡介苗可抑制气道炎症和气道重塑,降低TGF-β水平,上调E-钙黏蛋白表达,并下调α-SMA和Fn表达。本研究首次表明,哮喘慢性炎症诱导的TGF-β分泌增加可能导致EMT,这是哮喘所见气道炎症和气道重塑的最重要机制之一。卡介苗通过预防TGF-β诱导的EMT减轻气道炎症和气道重塑,因此卡介苗可能是一种治疗哮喘的新疗法。