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结核病——新药物、治疗方案、宿主导向疗法和生物标志物的研究进展。

Tuberculosis--advances in development of new drugs, treatment regimens, host-directed therapies, and biomarkers.

机构信息

Aurum Institute, Johannesburg, South Africa; Department of Medicine, Case Western Reserve University School of Medicine, Cleveland, OH, USA; Advancing Care for TB/HIV, Cape Town, South Africa.

Therapeutic Immunology, Departments of Laboratory Medicine and Microbiology, Tumour and Cell Biology, Karolinska Institute, Stockholm, Sweden.

出版信息

Lancet Infect Dis. 2016 Apr;16(4):e34-46. doi: 10.1016/S1473-3099(16)00070-0.

Abstract

Tuberculosis is the leading infectious cause of death worldwide, with 9·6 million cases and 1·5 million deaths reported in 2014. WHO estimates 480,000 cases of these were multidrug resistant (MDR). Less than half of patients who entered into treatment for MDR tuberculosis successfully completed that treatment, mainly due to high mortality and loss to follow-up. These in turn illustrate weaknesses in current treatment regimens and national tuberculosis programmes, coupled with operational treatment challenges. In this Review we provide an update on recent developments in the tuberculosis drug-development pipeline (including new and repurposed antimicrobials and host-directed drugs) as they are applied to new regimens to shorten and improve outcomes of tuberculosis treatment. Several new or repurposed antimicrobial drugs are in advanced trial stages for MDR tuberculosis, and two new antimicrobial drug candidates are in early-stage trials. Several trials to reduce the duration of therapy in MDR and drug-susceptible tuberculosis are ongoing. A wide range of candidate host-directed therapies are being developed to accelerate eradication of infection, prevent new drug resistance, and prevent permanent lung injury. As these drugs have been approved for other clinical indications, they are now ready for repurposing for tuberculosis in phase 2 clinical trials. We assess risks associated with evaluation of new treatment regimens, and highlight opportunities to advance tuberculosis research generally through regulatory innovation in MDR tuberculosis. Progress in tuberculosis-specific biomarkers (including culture conversion, PET and CT imaging, and gene expression profiles) can support this innovation. Several global initiatives now provide unique opportunities to tackle the tuberculosis epidemic through collaborative partnerships between high-income countries and middle-income and low-income countries for clinical trials training and research, allowing funders to coordinate several national and regional programmes for greatest overall effect.

摘要

结核病是全球导致死亡的首要传染病,2014 年报告发病 960 万例,死亡 150 万例。世卫组织估计,其中 48 万例为耐多药结核病。进入耐多药结核病治疗的患者中,不到一半成功完成治疗,主要原因是死亡率高和失访。这反过来又说明了现行治疗方案和国家结核病规划存在缺陷,再加上治疗操作方面的挑战。在本综述中,我们介绍了结核病药物研发管道(包括新的和重新利用的抗微生物药物和宿主导向药物)的最新进展,因为它们被应用于新的方案中,以缩短和改善结核病治疗的结果。有几种新的或重新利用的抗微生物药物处于耐多药结核病的后期试验阶段,有两种新的抗微生物候选药物处于早期试验阶段。有几个临床试验正在进行,以缩短耐多药和药物敏感结核病的治疗时间。正在开发广泛的宿主导向治疗候选药物,以加速清除感染,防止新的耐药性,并防止永久性肺损伤。由于这些药物已获准用于其他临床适应证,现在已准备好用于耐多药结核病的 2 期临床试验重新利用。我们评估了评估新治疗方案相关的风险,并强调了通过耐多药结核病监管创新推动结核病研究的机会。结核病特异性生物标志物(包括培养转换、PET 和 CT 成像以及基因表达谱)的进展可以支持这一创新。几个全球倡议现在通过高收入国家和中低收入国家之间的临床试验培训和研究合作伙伴关系,为通过协作伙伴关系应对结核病流行提供了独特的机会,使供资方能够协调几个国家和区域方案,以取得最大的总体效果。

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