Mattoli S
Avail Biomedical Research Institute, Scientific Direction and Project Management Centre, Basel, Switzerland.
Clin Exp Allergy. 2015 Oct;45(10):1497-509. doi: 10.1111/cea.12525.
Bloodborne fibrocytes are bone marrow-derived cells that participate in immune responses and exhibit pro-inflammatory and matrix remodelling properties. In patients with asthma receiving an adequate treatment, the blood fibrocyte count is very low and comparable to that obtained in healthy individuals. In these patients, a transient increase in fibrocyte numbers in the peripheral blood and in the airways occurs in concomitance with increased bronchial inflammation and reflects disease worsening and the need for more intensive treatment. Persistently elevated numbers of fibrocytes in the peripheral blood and in the bronchial mucosa are observed in chronically undertreated or corticosteroid-resistant asthma and are associated with persistent airway inflammation and ongoing remodelling of the bronchial wall. The asthmatic bronchial epithelium is the main source of fibrocyte chemoattractants in asthma and contributes with T helper type 2 lymphocytes and eosinophils to promote the proliferation and pro-remodelling function of recruited fibrocytes. The presence of elevated numbers of fibrocytes in the bronchial mucosa of allergic patients with undertreated or treatment-resistant asthma may also increase the risk of acute exacerbations because these cells can amplify T helper type 2 lymphocyte-driven inflammation on every exposure to the clinically relevant allergen and can promote further inflammation on rhinovirus infections by allowing viral replication and releasing additional pro-inflammatory factors. Improved methods for the isolation and functional analysis of pure populations of viable circulating fibrocytes have allowed a better understanding of the effector role of these cells. A reliable and clinically applicable assay has been developed to measure blood fibrocyte counts as outcome measure in future clinical trials. New therapeutic agents are needed to block both persistent inflammation and fibrocytosis in corticosteroid-resistant asthma.
血源纤维细胞是源自骨髓的细胞,参与免疫反应并具有促炎和基质重塑特性。在接受充分治疗的哮喘患者中,血纤维细胞计数非常低,与健康个体相当。在这些患者中,外周血和气道中纤维细胞数量的短暂增加与支气管炎症加剧同时出现,反映了疾病的恶化以及需要更强化的治疗。在外周血和支气管黏膜中持续出现纤维细胞数量升高的情况,见于长期治疗不足或对皮质类固醇耐药的哮喘患者,且与持续性气道炎症和支气管壁的持续重塑有关。哮喘支气管上皮是哮喘中纤维细胞趋化因子的主要来源,并与2型辅助性T淋巴细胞和嗜酸性粒细胞共同作用,促进募集的纤维细胞的增殖和促重塑功能。在未得到充分治疗或治疗抵抗的过敏性哮喘患者的支气管黏膜中,纤维细胞数量升高还可能增加急性加重的风险,因为这些细胞每次接触临床相关过敏原时都会放大2型辅助性T淋巴细胞驱动的炎症,并且在鼻病毒感染时通过允许病毒复制和释放额外的促炎因子来促进进一步的炎症。用于分离和功能分析活的循环纤维细胞纯群体的改进方法,使人们对这些细胞的效应作用有了更好的理解。已经开发出一种可靠且临床适用的检测方法,以测量血纤维细胞计数作为未来临床试验的结果指标。需要新的治疗药物来阻断皮质类固醇耐药性哮喘中的持续性炎症和纤维细胞增生。