Maitra Arundhati, Bates Sadé, Shaik Monisha, Evangelopoulos Dimitrios, Abubakar Ibrahim, McHugh Timothy D, Lipman Marc, Bhakta Sanjib
Mycobacteria Research Laboratory, Department of Biological Sciences, Institute of Structural and Molecular Biology, Birkbeck, University of London, Malet Street, London WC1E 7HX, UK.
Centre for Clinical Microbiology, University College London, London NW3 2PF, UK.
Br Med Bull. 2016 Jun;118(1):138-48. doi: 10.1093/bmb/ldw019. Epub 2016 May 5.
The number of cases of drug-resistant Mycobacterium tuberculosis, the causative agent of tuberculosis (TB), has risen rapidly in recent years. This has led to the resurgence in repurposing existing drugs, such as non-steroidal anti-inflammatory drugs (NSAIDs), for anti-TB treatment.
Evidence from novel drug screening in vitro, in vivo, pharmacokinetic/pharmacodynamics analyses and clinical trials has been used for the preparation of this systematic review of the potential of NSAIDs for use as an adjunct in new TB chemotherapies.
Certain NSAIDs have demonstrated inhibitory properties towards actively replicating, dormant and drug-resistant clinical isolates of M. tuberculosis cells.
NSAIDs are a diverse class of drugs, which have reported off-target activities, and their endogenous antimicrobial mechanism(s) of action is still unclear.
It is essential that clinical trials of NSAIDs continue, in order to assess their suitability for addition to the current TB treatment regimen. Repurposing molecules such as NSAIDs is a vital, low-risk strategy to combat the trend of rapidly increasing antibiotic resistance.
近年来,结核病的病原体——耐多药结核分枝杆菌病例数迅速上升。这导致人们重新关注现有药物,如非甾体抗炎药(NSAIDs),用于抗结核治疗。
来自体外新药筛选、体内研究、药代动力学/药效学分析和临床试验的证据已被用于编写本系统评价,以评估NSAIDs作为新的结核病化疗辅助药物的潜力。
某些NSAIDs已显示出对结核分枝杆菌细胞的活跃复制、休眠和耐药临床分离株具有抑制特性。
NSAIDs是一类多样的药物,有报道称其存在脱靶活性,其内在抗菌作用机制仍不清楚。
继续进行NSAIDs的临床试验至关重要,以便评估它们是否适合添加到当前的结核病治疗方案中。重新利用NSAIDs等分子是应对抗生素耐药性迅速增加趋势的重要且低风险策略。