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拯救最后一线多黏菌素:成就与挑战。

Rescuing the Last-Line Polymyxins: Achievements and Challenges.

机构信息

Biomedicine Discovery Institute and Department of Microbiology, Monash University, Melbourne, Victoria, Australia (S.C.N., M.A.K.A., J.L.); Department of Pharmacology and Therapeutics, School of Biomedical Sciences, Faculty of Medicine, Dentistry and Health Sciences, University of Melbourne, Melbourne, Victoria, Australia (T.V.); and Department of Industrial and Physical Pharmacy, College of Pharmacy, Purdue University, West Lafayette, Indiana (Q.T.Z.).

Biomedicine Discovery Institute and Department of Microbiology, Monash University, Melbourne, Victoria, Australia (S.C.N., M.A.K.A., J.L.); Department of Pharmacology and Therapeutics, School of Biomedical Sciences, Faculty of Medicine, Dentistry and Health Sciences, University of Melbourne, Melbourne, Victoria, Australia (T.V.); and Department of Industrial and Physical Pharmacy, College of Pharmacy, Purdue University, West Lafayette, Indiana (Q.T.Z.)

出版信息

Pharmacol Rev. 2021 Apr;73(2):679-728. doi: 10.1124/pharmrev.120.000020.

Abstract

Antibiotic resistance is a major global health challenge and, worryingly, several key Gram negative pathogens can become resistant to most currently available antibiotics. Polymyxins have been revived as a last-line therapeutic option for the treatment of infections caused by multidrug-resistant Gram negative bacteria, in particular , , and Enterobacterales. Polymyxins were first discovered in the late 1940s but were abandoned soon after their approval in the late 1950s as a result of toxicities (e.g., nephrotoxicity) and the availability of "safer" antibiotics approved at that time. Therefore, knowledge on polymyxins had been scarce until recently, when enormous efforts have been made by several research teams around the world to elucidate the chemical, microbiological, pharmacokinetic/pharmacodynamic, and toxicological properties of polymyxins. One of the major achievements is the development of the first scientifically based dosage regimens for colistin that are crucial to ensure its safe and effective use in patients. Although the guideline has not been developed for polymyxin B, a large clinical trial is currently being conducted to optimize its clinical use. Importantly, several novel, safer polymyxin-like lipopeptides are developed to overcome the nephrotoxicity, poor efficacy against pulmonary infections, and narrow therapeutic windows of the currently used polymyxin B and colistin. This review discusses the latest achievements on polymyxins and highlights the major challenges ahead in optimizing their clinical use and discovering new-generation polymyxins. To save lives from the deadly infections caused by Gram negative "superbugs," every effort must be made to improve the clinical utility of the last-line polymyxins. SIGNIFICANCE STATEMENT: Antimicrobial resistance poses a significant threat to global health. The increasing prevalence of multidrug-resistant (MDR) bacterial infections has been highlighted by leading global health organizations and authorities. Polymyxins are a last-line defense against difficult-to-treat MDR Gram negative pathogens. Unfortunately, the pharmacological information on polymyxins was very limited until recently. This review provides a comprehensive overview on the major achievements and challenges in polymyxin pharmacology and clinical use and how the recent findings have been employed to improve clinical practice worldwide.

摘要

抗生素耐药性是一个全球性的主要健康挑战,令人担忧的是,几种关键的革兰氏阴性病原体可能对目前大多数可用的抗生素产生耐药性。多粘菌素已被重新用作治疗多药耐药革兰氏阴性菌引起的感染的最后一线治疗选择,特别是鲍曼不动杆菌、铜绿假单胞菌和肠杆菌科。多粘菌素于 20 世纪 40 年代末首次发现,但在 20 世纪 50 年代末获得批准后不久就因毒性(如肾毒性)和当时批准的“更安全”抗生素的可用性而被弃用。因此,直到最近,当世界各地的几个研究团队做出巨大努力来阐明多粘菌素的化学、微生物学、药代动力学/药效学和毒理学特性时,人们才对多粘菌素有了更多的了解。其中一项主要成就是制定了第一个基于科学的多粘菌素 E 剂量方案,这对于确保其在患者中的安全有效使用至关重要。虽然尚未为多粘菌素 B 制定指南,但目前正在进行一项大型临床试验,以优化其临床应用。重要的是,为了克服目前使用的多粘菌素 B 和多粘菌素 E 的肾毒性、对肺部感染疗效差和治疗窗窄的问题,已经开发了几种新型、更安全的多粘菌素样脂肽。本文综述了多粘菌素的最新研究进展,并强调了在优化其临床应用和发现新一代多粘菌素方面面临的主要挑战。为了挽救革兰氏阴性“超级细菌”引起的致命感染,必须尽一切努力提高最后一线多粘菌素的临床实用性。

重要性声明

抗生素耐药性对全球健康构成重大威胁。多药耐药(MDR)细菌感染的日益流行已被全球主要卫生组织和当局所强调。多粘菌素是治疗难以治疗的 MDR 革兰氏阴性病原体的最后一道防线。不幸的是,直到最近,人们对多粘菌素的药理学信息知之甚少。本综述全面概述了多粘菌素药理学和临床应用方面的主要成就和挑战,以及最近的发现如何被用于改善全球的临床实践。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/884b/7911091/3001814378fe/pharmrev.120.000020absf1.jpg

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