Peterson M W, Monick M, Hunninghake G W
Chest. 1987 Jul;92(1):51-6. doi: 10.1378/chest.92.1.51.
Idiopathic pulmonary fibrosis (IPF) and pulmonary fibrosis associated with a collagen vascular disorder (PF-CVD) are chronic inflammatory lung disorders which may be characterized in various subgroups of patients by increased numbers of macrophages, neutrophils, lymphocytes, and/or eosinophils. Previous studies have suggested that the cell populations recovered with bronchoalveolar lavage (BAL) may be important in predicting disease progression and response to therapy. We evaluated this hypothesis in 27 patients by determining if the cell populations recovered with BAL differed between patients who improved, remained stable, or worsened in their pulmonary functions (as defined by at least a 15 percent change in forced vital capacity) over a six-month observation period. The findings suggested that BAL eosinophilia may be a marker of progressive lung disease in patients with IPF and PF-CVD.
特发性肺纤维化(IPF)和与胶原血管疾病相关的肺纤维化(PF-CVD)是慢性炎症性肺部疾病,在不同亚组患者中,其特征可能是巨噬细胞、中性粒细胞、淋巴细胞和/或嗜酸性粒细胞数量增加。先前的研究表明,通过支气管肺泡灌洗(BAL)回收的细胞群在预测疾病进展和治疗反应方面可能很重要。我们通过确定在六个月观察期内肺功能改善、保持稳定或恶化(定义为用力肺活量至少有15%的变化)的患者中,BAL回收的细胞群是否存在差异,对27名患者进行了这一假设的评估。研究结果表明,BAL嗜酸性粒细胞增多可能是IPF和PF-CVD患者进行性肺病的一个标志物。