Infection Innovative Medicines Unit, AstraZeneca R&D, Bangalore, India.
Antimicrob Agents Chemother. 2014;58(1):495-502. doi: 10.1128/AAC.01903-13. Epub 2013 Nov 4.
Treatment of tuberculosis (TB) is impaired by the long duration and complexity of therapy and the rising incidence of drug resistance. There is an urgent need for new agents with improved efficacy, safety, and compatibility with combination chemotherapies. Oxazolidinones offer a potential new class of TB drugs, and linezolid-the only currently approved oxazolidinone-has proven highly effective against extensively drug-resistant (XDR) TB in experimental trials. However, widespread use of linezolid is prohibited by its significant toxicities. AZD5847, a novel oxazolidinone, demonstrates improved in vitro bactericidal activity against both extracellular and intracellular M. tuberculosis compared to that of linezolid. Killing kinetics in broth media and in macrophages indicate that the rate and extent of kill obtained with AZD5847 are superior to those obtained with linezolid. Moreover, the efficacy of AZD5847 was additive when tested along with a variety of conventional TB agents, indicating that AZD5847 may function well in combination therapies. AZD5847 appears to function similarly to linezolid through impairment of the mycobacterial 50S ribosomal subunit. Future studies should be undertaken to further characterize the pharmacodynamics and pharmacokinetics of AZD5847 in both in vitro and animal models as well is in human clinical trials.
结核病(TB)的治疗受到治疗时间长、复杂性以及耐药性不断上升的影响。急需具有更高疗效、更高安全性且与联合化疗更兼容的新型药物。恶唑烷酮类药物提供了一种潜在的新型结核病药物,而利奈唑胺是目前唯一获批的恶唑烷酮,在实验性试验中已被证明对广泛耐药性(XDR)结核病具有高度疗效。然而,由于其严重的毒性,利奈唑胺的广泛使用受到限制。新型恶唑烷酮 AZD5847 与利奈唑胺相比,对细胞外和细胞内结核分枝杆菌均显示出体外杀菌活性的显著提高。在肉汤培养基和巨噬细胞中的杀菌动力学研究表明,AZD5847 的杀菌速度和程度优于利奈唑胺。此外,AZD5847 与多种常规结核病药物联合使用时具有增效作用,表明 AZD5847 可能在联合治疗中发挥良好作用。AZD5847 似乎通过抑制分枝杆菌 50S 核糖体亚基而与利奈唑胺发挥相似的作用。未来的研究应进一步在体外和动物模型中以及在人体临床试验中对 AZD5847 的药代动力学和药效学进行更全面的表征。