摘要
目前,耐多药结核病(Multidrug-resistant tuberculosis,MDR-TB)和广泛耐药结核病(Extensively drug-resistant tuberculosis,XDR-TB)治疗耗时长、方案复杂、药物毒性大、疗效差。MDR-TB治疗成功率低(52%)、病死率高(17%)、失访率高(15%),而XDR-TB治疗成功率仅26%,迫切需要开发新药和构建新化疗方案以提高疗效。德拉马尼(Delamanid,Dlm)在体内、外对处于复制、休眠期的结核分枝杆菌(Mycobacterium tuberculosis,MTB)均具有较强的杀灭作用。含Dlm的最佳背景方案(Optimised background regimen,OBR)治疗MDR-TB患者可增加2个月末的痰培养转阴率,并显著改善患者预后和降低病死率。本文主要对Dlm的药物特点、体外活性、动物实验、疗效和安全性的研究进展作一综述。
The treatment of multidrug-resistant tuberculosis(MDR-TB)and extensively drug-resistant tuberculosis(XDR-TB)is prone to more time-consuming,complex,toxic and ineffective.MDR-TB has low treatment success rate(52%)and high fatality rate(17%),as well as high rate of lost visits(15%),while the treatment success rate of XDR-TB is only 26%.It’s urgent to develop new drugs and chemotherapy regimens to improve the efficacy for MDR/XDR-TB.Delamanid(Dlm)has a strong killing effect on Mycobacterium tuberculosis(MTB)in vitro and in vivo.When MDR-TB patients are treated with optimized background regimen containing Dlm,the two-month sputum negative conversion rate is increased,case fatality is decreased and the prognosis is improved.This article reviews the progress on characteristics,in vitro activity,animal tests,clinical efficacy and safety of Dlm.
作者
王乐乐
杨松
Wang Lele;Yang Song(Chongqing Public Health Medical Center,Chongqing 400036,China)
出处
《中华临床感染病杂志》
CSCD
2020年第4期315-320,共6页
Chinese Journal of Clinical Infectious Diseases
基金
重庆市卫生健康委员会、重庆市科学技术局联合医学科研计划(2019ZDXM035)
重庆市卫生计生委医学科研项目(2019MSXM065)。
关键词
德拉马尼
耐多药结核病
广泛耐药结核病
疗效
安全性
Delamanid
Multidrug-resistant tuberculosis
Extensive drug-resistant tuberculosis
Efficacy
Safety