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新型多黏菌素类抗生素的发现。

Discovery of Novel Polymyxin-Like Antibiotics.

机构信息

Department of Pharmacology and Therapeutics, University of Melbourne, Parkville, VIC, Australia.

Biomedicine Discovery Institute and Department of Microbiology, Monash University, Clayton, VIC, Australia.

出版信息

Adv Exp Med Biol. 2019;1145:343-362. doi: 10.1007/978-3-030-16373-0_20.

Abstract

The antimicrobial lipopeptides polymyxin B and colistin (polymyxin E) are used as a 'last-line' therapy for infections caused by multidrug-resistant (MDR) Gram-negative pathogens. However, their effective use as antibiotic drugs in the clinical setting is still plagued by significant toxicity issues, in particular their potential for nephrotoxicity. Furthermore, resistance to the polymyxins has begun to emerge in the clinic, which implies a total lack of antibiotics for the treatment of life-threatening infections caused by the Gram-negative 'superbugs'. This chapter details our current understanding of polymyxin structure-activity relationships as well as recent pre-clinical and clinical drug development efforts aimed at generating new polymyxin antibiotics with improved safety and efficacy.

摘要

抗菌脂肽多黏菌素 B 和多黏菌素 E(多黏菌素)被用作治疗多重耐药(MDR)革兰氏阴性病原体引起的感染的“最后一线”疗法。然而,它们在临床环境中作为抗生素药物的有效使用仍然受到严重毒性问题的困扰,特别是它们潜在的肾毒性。此外,对多黏菌素的耐药性已开始在临床上出现,这意味着对于革兰氏阴性“超级细菌”引起的危及生命的感染,完全没有抗生素可用。本章详细介绍了我们目前对多黏菌素结构-活性关系的理解,以及最近旨在生成具有更好安全性和疗效的新型多黏菌素抗生素的临床前和临床药物开发工作。

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