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复苏多黏菌素:成就、经验教训和未来之路。

Reviving Polymyxins: Achievements, Lessons and the Road Ahead.

机构信息

Biomedicine Discovery Institute, Infection & Immunity Program and Department of Microbiology, Monash University, Clayton Campus, Melbourne, VIC, Australia.

出版信息

Adv Exp Med Biol. 2019;1145:1-8. doi: 10.1007/978-3-030-16373-0_1.

DOI:10.1007/978-3-030-16373-0_1
PMID:31364067
Abstract

Antibiotic resistance has become the most significant threat to human health across the globe. Polymyxins are often used as the only available therapeutic option against Gram-negative 'superbugs', namely Acinetobacter baumannii, Pseudomonas aeruginosa and Klebsiella pneumoniae. The limited pharmacological and clinical knowledge on the polymyxins in the old literature substantially limited optimizing their clinical use. The current chapter provides a general introduction to this first-ever polymyxin book which comprehensively reviews the significant progress over the last two decades in the chemistry, microbiology, pharmacology, clinical use and drug discovery of polymyxins. In particular, recent pharmacological results have led to the first scientifically-based dosing recommendations and facilitated the discovery of new-generation polymyxins. Future challenges in polymyxin research are highlighted, aiming at improving the clinical utility of this last-line defence.

摘要

抗生素耐药性已成为全球范围内对人类健康的最大威胁。多黏菌素通常被用作针对革兰氏阴性“超级细菌”(即鲍曼不动杆菌、铜绿假单胞菌和肺炎克雷伯菌)的唯一有效治疗选择。旧文献中关于多黏菌素的药理学和临床知识有限,极大地限制了其临床应用的优化。本章提供了有史以来第一本多黏菌素书籍的概述,全面回顾了过去二十年在多黏菌素的化学、微生物学、药理学、临床应用和药物发现方面的重要进展。特别是,最近的药理学研究结果导致了首次基于科学的剂量建议,并促进了新一代多黏菌素的发现。突出了多黏菌素研究中的未来挑战,旨在提高这种最后防线药物的临床实用性。

相似文献

1
Reviving Polymyxins: Achievements, Lessons and the Road Ahead.复苏多黏菌素:成就、经验教训和未来之路。
Adv Exp Med Biol. 2019;1145:1-8. doi: 10.1007/978-3-030-16373-0_1.
2
Multidrug-Resistant Gram-Negative Pathogens: The Urgent Need for 'Old' Polymyxins.耐多药革兰氏阴性病原体:急需“老”多黏菌素。
Adv Exp Med Biol. 2019;1145:9-13. doi: 10.1007/978-3-030-16373-0_2.
3
Synergistic combinations of polymyxins.多粘菌素的协同组合。
Int J Antimicrob Agents. 2016 Dec;48(6):607-613. doi: 10.1016/j.ijantimicag.2016.09.014. Epub 2016 Oct 24.
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History, Chemistry and Antibacterial Spectrum.历史、化学和抗菌谱。
Adv Exp Med Biol. 2019;1145:15-36. doi: 10.1007/978-3-030-16373-0_3.
5
Rescuing the Last-Line Polymyxins: Achievements and Challenges.拯救最后一线多黏菌素:成就与挑战。
Pharmacol Rev. 2021 Apr;73(2):679-728. doi: 10.1124/pharmrev.120.000020.
6
Resistance to polymyxins in Gram-negative organisms.革兰氏阴性菌对多黏菌素的耐药性。
Int J Antimicrob Agents. 2017 May;49(5):526-535. doi: 10.1016/j.ijantimicag.2016.11.029. Epub 2017 Feb 3.
7
Pharmacology of polymyxins: new insights into an 'old' class of antibiotics.多黏菌素类抗生素的药理学:对一类“老”抗生素的新认识。
Future Microbiol. 2013 Jun;8(6):711-24. doi: 10.2217/fmb.13.39.
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Polymyxins for the treatment of lower respiratory tract infections: lessons learned from the integration of clinical pharmacokinetic studies and clinical outcomes.多黏菌素治疗下呼吸道感染:从药代动力学研究与临床结局整合中汲取的经验教训。
Int J Antimicrob Agents. 2021 Jun;57(6):106328. doi: 10.1016/j.ijantimicag.2021.106328. Epub 2021 Mar 27.
9
Polymyxins: a new hope in combating Gram-negative superbugs?多黏菌素:对抗革兰氏阴性超级细菌的新希望?
Future Med Chem. 2016 Jun;8(10):1017-25. doi: 10.4155/fmc-2016-0091. Epub 2016 Jun 21.
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Rediscovering the octapeptins.重新发现八肽菌素。
Nat Prod Rep. 2017 Mar 17;34(3):295-309. doi: 10.1039/c6np00113k.

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The pharmacokinetic-nephrotoxicity relationships of CMS and CMS-E2 from the perspective of plasma and kidney drug concentrations in rats.从大鼠血浆和肾脏药物浓度的角度探讨CMS和CMS-E2的药代动力学-肾毒性关系。
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Risk Factors for Acute Kidney Injury Induced by Intravenous Polymyxin B in Chinese Patients with Severe Infection.
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Infect Drug Resist. 2022 Apr 19;15:1957-1965. doi: 10.2147/IDR.S363944. eCollection 2022.
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Small Molecule Inhibitors of the Bacterioferritin (BfrB)-Ferredoxin (Bfd) Complex Kill Biofilm-Embedded Cells.细菌铁蛋白(BfrB)-铁氧化还原蛋白(Bfd)复合物的小分子抑制剂可杀死生物膜包裹的细胞。
ACS Infect Dis. 2021 Jan 8;7(1):123-140. doi: 10.1021/acsinfecdis.0c00669. Epub 2020 Dec 3.
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Polymyxin-Induced Cell Death of Human Macrophage-Like THP-1 and Neutrophil-Like HL-60 Cells Associated with the Activation of Apoptotic Pathways.多粘菌素诱导人巨噬细胞样THP-1细胞和中性粒细胞样HL-60细胞死亡,与凋亡途径的激活有关。
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