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新型抗结核药物

New Drugs for the Treatment of Tuberculosis.

机构信息

Department of Medicine, Johns Hopkins University School of Medicine, 1830 Building Room 450B, 1830 East Monument Street, Baltimore, MD 21287, USA.

Department of Medicine, Center for Tuberculosis Research, Johns Hopkins University School of Medicine, 600 North Wolfe Street, Osler 527, Baltimore, MD, USA.

出版信息

Clin Chest Med. 2019 Dec;40(4):811-827. doi: 10.1016/j.ccm.2019.08.001.

DOI:10.1016/j.ccm.2019.08.001
PMID:31731986
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9178517/
Abstract

Tuberculosis (TB) has now surpassed HIV as the leading infectious cause of death, and treatment success rates are declining. Multidrug-resistant TB, extensively drug-resistant TB, and even totally drug-resistant TB threaten to further destabilize disease control efforts. The second wave in TB drug development, which includes the diarylquinoline, bedaquiline, and the nitroimidazoles delamanid and pretomanid, may offer options for simpler, shorter, and potentially all-oral regimens to treat drug-resistant TB. The "third wave" of TB drug development includes numerous promising compounds, including less toxic versions of older drug classes and candidates with novel mechanisms of action.

摘要

结核病(TB)现已超过艾滋病毒,成为导致死亡的主要传染病,且治疗成功率正在下降。耐多药结核病、广泛耐药结核病,甚至完全耐药结核病有可能进一步破坏疾病控制工作。TB 药物研发的第二波浪潮包括二芳基喹啉、贝达喹啉以及硝基咪唑类药物德拉马尼和普雷托马尼,它们可能为治疗耐药性结核病提供更简单、更短、且可能全口服的方案选择。TB 药物研发的“第三波浪潮”包括许多有前途的化合物,包括毒性较小的旧药类别和具有新型作用机制的候选药物。

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本文引用的文献

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Mutations in () as a Novel Determinant of Resistance to Pretomanid and Delamanid in Mycobacterium tuberculosis.() 突变是导致结核分枝杆菌对丙硫异烟胺和德拉马尼耐药的新决定因素。
Antimicrob Agents Chemother. 2020 Dec 16;65(1). doi: 10.1128/AAC.01948-20.
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Delamanid Central Nervous System Pharmacokinetics in Tuberculous Meningitis in Rabbits and Humans.德拉马尼在兔和人类结核性脑膜炎中的中枢神经系统药代动力学研究。
Antimicrob Agents Chemother. 2019 Sep 23;63(10). doi: 10.1128/AAC.00913-19. Print 2019 Oct.
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Efficacy and safety of delamanid in combination with an optimised background regimen for treatment of multidrug-resistant tuberculosis: a multicentre, randomised, double-blind, placebo-controlled, parallel group phase 3 trial.德拉马尼联合优化背景治疗方案治疗耐多药结核病的疗效和安全性:一项多中心、随机、双盲、安慰剂对照、平行分组 3 期临床试验。
Lancet Respir Med. 2019 Mar;7(3):249-259. doi: 10.1016/S2213-2600(18)30426-0. Epub 2019 Jan 7.
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A patient-level pooled analysis of treatment-shortening regimens for drug-susceptible pulmonary tuberculosis.药物敏感性肺结核治疗缩短方案的患者水平汇总分析。
Nat Med. 2018 Nov;24(11):1708-1715. doi: 10.1038/s41591-018-0224-2. Epub 2018 Nov 5.
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High treatment success rate for multidrug-resistant and extensively drug-resistant tuberculosis using a bedaquiline-containing treatment regimen.含贝达喹啉治疗方案治疗耐多药和广泛耐药结核病的高治疗成功率。
Eur Respir J. 2018 Dec 20;52(6). doi: 10.1183/13993003.01528-2018. Print 2018 Dec.
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Treatment correlates of successful outcomes in pulmonary multidrug-resistant tuberculosis: an individual patient data meta-analysis.肺耐多药结核病成功治疗结果的相关因素:一项个体患者数据荟萃分析。
Lancet. 2018 Sep 8;392(10150):821-834. doi: 10.1016/S0140-6736(18)31644-1.
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Improved Treatment Outcomes With Bedaquiline When Substituted for Second-line Injectable Agents in Multidrug-resistant Tuberculosis: A Retrospective Cohort Study.贝达喹啉替代二线注射剂治疗耐多药结核病的疗效改善:一项回顾性队列研究。
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Optimized Background Regimen for Treatment of Active Tuberculosis with the Next-Generation Benzothiazinone Macozinone (PBTZ169).优化背景治疗方案治疗活动期结核病与下一代苯并噻嗪酮 Macozinone (PBTZ169)。
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