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依拉卡托非/泰他卡托非/艾维雷司他韦联合治疗根除囊性纤维化患者分枝杆菌脓肿感染。

Eradication of Mycobacterium abscessus infection in cystic fibrosis with initiation of Elexacaftor/Tezacaftor/Ivacaftor.

机构信息

Department of Medicine, Dalhousie University, Halifax, NS, Canada.

Division of Respirology, Dalhousie University, Halifax, NS, Canada.

出版信息

J Cyst Fibros. 2024 Jan;23(1):38-40. doi: 10.1016/j.jcf.2023.03.021. Epub 2023 Apr 17.

Abstract

Mycobacterium abscessus is a nontuberculous mycobacterium that is often multi-drug resistant, difficult to eradicate and associated with a rapid decline in lung function in cystic fibrosis (CF). Elexacaftor/Tezacaftor/Ivacaftor (ETI) is a combination CFTR modulator that improves lung function and decreases exacerbations, but limited data exists about its impact on respiratory infections. A 23-year-old male with CF (F508del, unknown) was diagnosed with Mycobacterium abscessus subspecies abscessus infection. He completed 12-weeks of intensive therapy, followed by oral continuation therapy. Antimicrobials were later discontinued for optic neuritis secondary to linezolid. He remained off antimicrobials with persistently positive sputum cultures. He then initiated ETI, and bronchoscopy eight months later suggested eradication of M. abscessus. By modulating CFTR protein function, ETI may improve innate airway defence mechanisms, facilitating the clearance of infections such as M. abscessus. This case highlights the potential positive implications of ETI on the challenging treatment of M. abscessus infections in CF.

摘要

脓肿分枝杆菌是一种非结核分枝杆菌,通常具有多重耐药性,难以根除,并与囊性纤维化 (CF) 患者的肺功能迅速下降有关。Elexacaftor/Tezacaftor/Ivacaftor(ETI)是一种 CFTR 调节剂的联合用药,可改善肺功能并减少恶化,但关于其对呼吸道感染的影响的数据有限。一名 23 岁的男性 CF 患者(F508del,未知)被诊断为脓肿分枝杆菌亚种脓肿感染。他完成了 12 周的强化治疗,随后进行了口服维持治疗。由于利奈唑胺引起的视神经炎,后来停止使用抗生素。由于持续的痰培养阳性,他一直未使用抗生素。然后他开始使用 ETI,八个月后的支气管镜检查提示脓肿分枝杆菌已被根除。通过调节 CFTR 蛋白功能,ETI 可能改善先天气道防御机制,有助于清除脓肿分枝杆菌等感染。本病例强调了 ETI 在 CF 患者中治疗脓肿分枝杆菌感染的挑战性方面具有潜在的积极意义。

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