Bottlenecks and opportunities in antibiotic discovery against Mycobacterium tuberculosis

被引:12
|
作者
Craggs, Peter D. [1 ,2 ]
de Carvalho, Luiz Pedro S. [1 ]
机构
[1] Francis Crick Inst, Mycobacterial Metab & Antibiot Res Lab, London NW1 1AT, England
[2] GlaxoSmithKline, GSK Francis Crick Inst, Linklabs Med Sci & Technol, Stevenage SG1 2NY, England
基金
英国惠康基金; 英国医学研究理事会;
关键词
ANTITUBERCULOSIS AGENTS; BETA-LACTAMASE; DRUG DISCOVERY; INHIBITION;
D O I
10.1016/j.mib.2022.102191
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Tuberculosis (TB) persists as a major global health issue and a leading cause of death by a single infectious agent. The global burden of TB is further exacerbated by the continuing emergence and dissemination of strains of Mycobacterium tuberculosis resistant to multiple antibiotics. The need for novel drugs that can be used to shorten the course for current TB drug regimens as well as combat the persistent threat of antibiotic resistance has never been greater. There have been significant advances in the discovery of de novo TB treatments, with the first TB-specific drugs in 45 years approved for use. However, there are still issues that restrict the pipeline of new antitubercular chemotherapies. The rate of failure of TB drug candidates in clinical trials remains high, while the validation of new TB drug targets and subsequent identification of novel inhibitors remains modest.
引用
收藏
页数:8
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