Division of Infectious Diseases, Department of Medicine, School of Medicine, Johns Hopkins University, Baltimore, Maryland, USA.
Center for Nontuberculous Mycobacteria and Bronchiectasis, School of Medicine, Johns Hopkins University, Baltimore, Maryland, USA.
Antimicrob Agents Chemother. 2024 Aug 7;68(8):e0064824. doi: 10.1128/aac.00648-24. Epub 2024 Jul 17.
( or ) is a fast-growing mycobacterium that is ubiquitous in the environment and can cause opportunistic disease in people with lung comorbidity and immunodeficiency. There are no Food and Drug Administration-approved drugs for this disease, and repurposed antibiotics have a poor microbiological response. To address the need for effective new antibiotics, we determined the efficacy of epetraborole (EBO) against three clinical isolates in a mouse model of lung infection. Reduction in lung burden over 4 weeks of treatment was the study end point. EBO was administered orally once daily at doses of 25 and 50 mg/kg, which achieved exposures approximating the once-daily dosing of 250 mg and 500 mg, respectively, in humans. EBO administration led to a gradual reduction in the lung burden. After 4 weeks of treatment, the efficacies of 25 and 50 mg/kg EBO against isolates ATCC 19977 and M9501 were comparable. However, against isolate M9530, 50 mg/kg EBO was more efficacious than 25 mg/kg and comparable with parenteral imipenem, one of the most efficacious antibiotics against . We also undertook a dose-ranging study by evaluating the efficacies of once-daily oral administration of 0.5, 5, 10, 25, and 100 mg/kg EBO against M9501 over 4 weeks. Once-daily oral 100 mg/kg EBO was as effective as twice-daily 100 mg/kg imipenem injection. Our study suggests that EBO could address the unmet need for effective oral treatment options for lung disease, given the high rates of drug resistance and limited tolerable intravenous options.
(或)是一种快速生长的分枝杆菌,在环境中无处不在,可导致肺部合并症和免疫功能低下的人发生机会性疾病。目前尚无针对这种疾病的美国食品和药物管理局批准的药物,而重新利用的抗生素的微生物反应较差。为了解决有效新抗生素的需求,我们在肺部感染的小鼠模型中确定了埃培拉博尔(EBO)对三种临床分离株的疗效。治疗 4 周后肺部负荷的减少是研究终点。EBO 每天口服一次,剂量为 25 和 50mg/kg,分别在人体中达到了每天一次 250mg 和 500mg 的近似暴露量。EBO 给药导致肺部负荷逐渐减少。经过 4 周的治疗,25 和 50mg/kg EBO 对 ATCC 19977 和 M9501 分离株的疗效相当。然而,对 M9530 分离株,50mg/kg EBO 的疗效优于 25mg/kg,与最有效的抗生素之一——注射用亚胺培南相当。我们还通过评估每天口服 0.5、5、10、25 和 100mg/kg EBO 对 M9501 的疗效,进行了剂量范围研究,共 4 周。每天口服 100mg/kg EBO 与每天两次 100mg/kg 注射用亚胺培南的疗效相同。鉴于耐药率高且静脉耐受有限的选择,我们的研究表明,EBO 可能满足治疗肺部疾病的有效口服治疗方案的未满足需求。