Yamaguchi Masafumi, Yamazaki Akio, Nakagawa Hiroaki, Kinose Daisuke, Nakano Yasutaka
Division of Respiratory Medicine, Department of Internal Medicine, Shiga University of Medical Science, Otsu, Japan.
J Asthma Allergy. 2025 Aug 28;18:1221-1227. doi: 10.2147/JAA.S541770. eCollection 2025.
Allergic bronchopulmonary aspergillosis is characterized by hypersensitivity to spp. and often causes intractable asthma. Studies have been conducted on biologics administered to patients with allergic bronchopulmonary aspergillosis; however, treatment may not always be successful. This may be due to the limitations of the current biologics that selectively target a single cytokine. Tezepelumab, a human monoclonal antibody that blocks the activity of thymic stromal lymphopoietin, broadly suppresses type 2 inflammation by regulating the upstream cascade of airway inflammation. Therefore, it is expected to have favorable effects in patients with allergic bronchopulmonary aspergillosis. We report three cases of allergic bronchopulmonary aspergillosis with uncontrolled symptoms despite the maximal use of conventional anti-asthmatic drugs such as inhalative agents, anti-leukotriene receptor antagonists, and antifungal drugs. None of the patients had previously received biologics. The addition of tezepelumab produced a marked clinical response in all three patients, which included fewer exacerbations and a reduced dosage of oral systemic corticosteroids and/or reduced as-needed short-acting beta-2 agonists. The patients' pulmonary symptoms were better controlled, peripheral blood eosinophil counts and immunoglobulin E levels decreased, and quality of life scores and respiratory function parameters improved. Mucous plugs accompanied by atelectasis and infiltrative shadows observed on chest computed tomography also improved. Tezepelumab may be a promising treatment option for allergic bronchopulmonary aspergillosis in patients with severe asthma, offering effective symptom control and enabling reduction in systemic corticosteroid use.
变应性支气管肺曲霉病的特征是对曲霉属物种过敏,常导致难治性哮喘。已有针对变应性支气管肺曲霉病患者使用生物制剂的研究;然而,治疗并非总能成功。这可能是由于目前选择性靶向单一细胞因子的生物制剂存在局限性。tezepelumab是一种阻断胸腺基质淋巴细胞生成素活性的人单克隆抗体,通过调节气道炎症的上游级联反应广泛抑制2型炎症。因此,预计它对变应性支气管肺曲霉病患者有良好疗效。我们报告了3例变应性支气管肺曲霉病患者,尽管最大程度地使用了吸入剂、抗白三烯受体拮抗剂和抗真菌药物等传统抗哮喘药物,但症状仍未得到控制。所有患者此前均未接受过生物制剂治疗。添加tezepelumab后,所有3例患者均产生了显著的临床反应,包括病情加重次数减少、口服全身性皮质类固醇剂量降低和/或按需使用的短效β2激动剂减少。患者的肺部症状得到更好控制,外周血嗜酸性粒细胞计数和免疫球蛋白E水平下降,生活质量评分和呼吸功能参数改善。胸部计算机断层扫描显示的伴有肺不张的黏液栓和浸润影也有所改善。对于重度哮喘合并变应性支气管肺曲霉病的患者,tezepelumab可能是一种有前景的治疗选择,可有效控制症状并减少全身性皮质类固醇的使用。