Lamont Elise A, Dillon Nicholas A, Baughn Anthony D
Department of Microbiology and Immunology, University of Minnesota Medical School, Minneapolis, Minnesota, USA.
Department of Microbiology and Immunology, University of Minnesota Medical School, Minneapolis, Minnesota, USA
Microbiol Mol Biol Rev. 2020 Mar 4;84(2). doi: 10.1128/MMBR.00070-19. Print 2020 May 20.
Pyrazinamide (PZA) is a cornerstone antimicrobial drug used exclusively for the treatment of tuberculosis (TB). Due to its ability to shorten drug therapy by 3 months and reduce disease relapse rates, PZA is considered an irreplaceable component of standard first-line short-course therapy for drug-susceptible TB and second-line treatment regimens for multidrug-resistant TB. Despite over 60 years of research on PZA and its crucial role in current and future TB treatment regimens, the mode of action of this unique drug remains unclear. Defining the mode of action for PZA will open new avenues for rational design of novel therapeutic approaches for the treatment of TB. In this review, we discuss the four prevailing models for PZA action, recent developments in modulation of PZA susceptibility and resistance, and outlooks for future research and drug development.
吡嗪酰胺(PZA)是一种专门用于治疗结核病(TB)的基石性抗菌药物。由于其能够将药物治疗疗程缩短3个月并降低疾病复发率,PZA被认为是敏感结核病一线标准短程治疗以及耐多药结核病二线治疗方案中不可替代的组成部分。尽管对PZA已经进行了60多年的研究,且其在当前和未来结核病治疗方案中发挥着关键作用,但这种独特药物的作用方式仍不明确。明确PZA的作用方式将为合理设计治疗结核病的新型治疗方法开辟新途径。在本综述中,我们讨论了PZA作用的四种主流模型、PZA敏感性和耐药性调控的最新进展以及未来研究和药物开发的前景。