Department of Microbiology, Yonsei University College of Medicine, Seoul, South Korea.
Institute for Immunology and Immunological Disease, Yonsei University College of Medicine, Seoul, South Korea.
Antimicrob Agents Chemother. 2022 Sep 20;66(9):e0076222. doi: 10.1128/aac.00762-22. Epub 2022 Aug 30.
Accumulating evidence suggests that drug repurposing has drawn attention as an anticipative strategy for controlling tuberculosis (TB), considering the dwindling drug discovery and development pipeline. In this study, we explored the antigout drug febuxostat and evaluated its antibacterial activity against Mycobacterium species. Based on MIC evaluation, we found that febuxostat treatment significantly inhibited mycobacterial growth, especially that of Mycobacterium tuberculosis (Mtb) and its phylogenetically close neighbors, M. bovis, M. kansasii, and M. shinjukuense, but these microorganisms were not affected by allopurinol and topiroxostat, which belong to a similar category of antigout drugs. Febuxostat concentration-dependently affected Mtb and durably mediated inhibitory functions (duration, 10 weeks maximum), as evidenced by resazurin microtiter assay, time-kill curve analysis, phenotypic susceptibility test, and the Bactec MGIT 960 system. Based on these results, we determined whether the drug shows antimycobacterial activity against Mtb inside murine bone marrow-derived macrophages (BMDMs). Notably, febuxostat markedly suppressed the intracellular growth of Mtb in a dose-dependent manner without affecting the viability of BMDMs. Moreover, orally administered febuxostat was efficacious in a murine model of TB with reduced bacterial loads in both the lung and spleen without the exacerbation of lung inflammation, which highlights the drug potency. Taken together, unexpectedly, our data demonstrated that febuxostat has the potential for treating TB.
越来越多的证据表明,考虑到药物发现和开发管道的减少,药物重定位已成为控制结核病 (TB) 的一种预期策略,引起了人们的关注。在这项研究中,我们探索了抗痛风药物非布司他,并评估了其对分枝杆菌属的抗菌活性。基于 MIC 评估,我们发现非布司他治疗可显著抑制分枝杆菌的生长,尤其是结核分枝杆菌 (Mtb) 及其亲缘关系密切的分枝杆菌,如牛分枝杆菌、堪萨斯分枝杆菌和辛久京分枝杆菌,但这些微生物不受别嘌醇和托匹司他的影响,别嘌醇和托匹司他属于类似的抗痛风药物类别。非布司他浓度依赖性地影响 Mtb 并持久介导抑制功能(最长 10 周),如 Resazurin 微量滴定测定、时间杀伤曲线分析、表型药敏试验和 Bactec MGIT 960 系统所证实。基于这些结果,我们确定该药物是否对 Mtb 在鼠骨髓来源的巨噬细胞 (BMDM) 内显示抗分枝杆菌活性。值得注意的是,非布司他以剂量依赖性方式显著抑制 Mtb 的细胞内生长,而不影响 BMDM 的活力。此外,口服给予非布司他在 TB 小鼠模型中有效,可降低肺部和脾脏中的细菌负荷,而不加重肺部炎症,突出了药物的功效。总的来说,出乎意料的是,我们的数据表明非布司他具有治疗结核病的潜力。