Tracy Michael C, Okorie Caroline U A, Foley Elizabeth A, Moss Richard B
Center for Excellence in Pulmonary Biology, Department of Pediatrics, Stanford University School of Medicine, 770 Welch Road suite 350, Palo Alto, CA 94304, USA.
J Fungi (Basel). 2016 Jun 6;2(2):17. doi: 10.3390/jof2020017.
Allergic bronchopulmonary aspergillosis (ABPA), a progressive fungal allergic lung disease, is a common complication of asthma or cystic fibrosis. Although ABPA has been recognized since the 1950s, recent research has underscored the importance of Th2 immune deviation and granulocyte activation in its pathogenesis. There is also strong evidence of widespread under-diagnosis due to the complexity and lack of standardization of diagnostic criteria. Treatment has long focused on downregulation of the inflammatory response with prolonged courses of oral glucocorticosteroids, but more recently concerns with steroid toxicity and availability of new treatment modalities has led to trials of oral azoles, inhaled amphotericin, pulse intravenous steroids, and subcutaneously-injected anti-IgE monoclonal antibody omalizumab, all of which show evidence of efficacy and reduced toxicity.
变应性支气管肺曲霉病(ABPA)是一种进行性真菌过敏性肺部疾病,是哮喘或囊性纤维化的常见并发症。尽管自20世纪50年代以来就已认识到ABPA,但最近的研究强调了Th2免疫偏移和粒细胞活化在其发病机制中的重要性。由于诊断标准复杂且缺乏标准化,也有强有力的证据表明存在广泛的诊断不足。长期以来,治疗一直侧重于通过长期口服糖皮质激素来下调炎症反应,但最近对类固醇毒性的担忧以及新治疗方式的出现,导致了口服唑类、吸入两性霉素、脉冲静脉注射类固醇和皮下注射抗IgE单克隆抗体奥马珠单抗的试验,所有这些都显示出疗效证据且毒性降低。