Erkoç Merve, Aydın Ömür, Bavbek Sevim
Division of İmmunology and Allergy, Department of Chest Diseases, Ankara University Faculty of Medicine, Ankara, Turkey.
Tuberk Toraks. 2021 Mar;69(1):84-93. doi: 10.5578/tt.20219910.
Allergic Bronchopulmonary Aspergillosis (ABPA) is a pulmonary disease characterized by recurrent pulmonary opacities and bronchiectasis caused by Type 1 hypersensitivity to A. fumigatus. Asthma is an important part of the disease and is generally in severe form. It is thought that immunoglobulins against A. fumigatus, Th2-derived cytokines such as IL-4, IL-5 and IL-13 and eosinophilic inflammation play a role in the pathogenesis of the disease. Monoclonal antibody treatments targeting IL-4, IL-5, IL-13 and IgE, which are involved in pathogenesis, have been used in asthmatic patients before. The main treatment of ABPA for exacerbations and remissions is oral corticosteroids (OCS). However, in cases where the corticosteroid dose cannot be reduced or side effects develop, monoclonal agents may be added to the treatment. Monoclonal agents such as omalizumab, mepolizumab, benralizumab and dupilumab targeting cytokines involved to the patogenesis have been used in patients with ABPA. Omalizumab has shown a reduction in exacerbations and OCS requirements, improvement in asthma symptoms and improvement in pulmonary function parameters. With mepolizumab, a decrease in OCS dose, decrease in blood eosinophil count, clinical improvement and radiological improvement were observed. Benralizumab reduced, the number of eosinophil or even almost nullified as well as clinical recovery alongside with radiological improvement. With dupilumab, improvement in symptoms, discontinuation of OCS, but increase in eosinophil count at the beginning of treatment was reported. As a result, monoclonal antibodies were generally found to be successful and safe in patients with ABPA.
变应性支气管肺曲霉病(ABPA)是一种肺部疾病,其特征为对烟曲霉的1型超敏反应导致反复出现肺部混浊和支气管扩张。哮喘是该疾病的重要组成部分,且通常较为严重。据认为,针对烟曲霉的免疫球蛋白、Th2衍生的细胞因子如白细胞介素-4(IL-4)、白细胞介素-5(IL-5)和白细胞介素-13以及嗜酸性粒细胞炎症在该疾病的发病机制中起作用。此前,针对参与发病机制的IL-4、IL-5、IL-13和IgE的单克隆抗体疗法已用于哮喘患者。ABPA急性加重期和缓解期的主要治疗方法是口服糖皮质激素(OCS)。然而,在无法减少糖皮质激素剂量或出现副作用的情况下,可在治疗中添加单克隆药物。针对参与发病机制的细胞因子的单克隆药物,如奥马珠单抗、美泊利单抗、贝那利珠单抗和度普利尤单抗,已用于ABPA患者。奥马珠单抗已显示出可减少急性加重次数和对OCS的需求,改善哮喘症状并改善肺功能参数。使用美泊利单抗时,观察到OCS剂量减少、血液嗜酸性粒细胞计数降低、临床改善和影像学改善。贝那利珠单抗减少了嗜酸性粒细胞数量甚至几乎使其归零,同时临床恢复并伴有影像学改善。使用度普利尤单抗时,报告症状改善、停用OCS,但在治疗开始时嗜酸性粒细胞计数增加。结果,一般发现单克隆抗体对ABPA患者有效且安全。