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抗生素新纪元:抗菌肽的临床潜力。

A New Era of Antibiotics: The Clinical Potential of Antimicrobial Peptides.

机构信息

School of Chemistry, University of New South Wales (UNSW) Sydney, Sydney 2052, Australia.

School of Optometry and Vision Science, University of New South Wales (UNSW) Sydney, Sydney 2052, Australia.

出版信息

Int J Mol Sci. 2020 Sep 24;21(19):7047. doi: 10.3390/ijms21197047.


DOI:10.3390/ijms21197047
PMID:32987946
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7582481/
Abstract

Antimicrobial resistance is a multifaceted crisis, imposing a serious threat to global health. The traditional antibiotic pipeline has been exhausted, prompting research into alternate antimicrobial strategies. Inspired by nature, antimicrobial peptides are rapidly gaining attention for their clinical potential as they present distinct advantages over traditional antibiotics. Antimicrobial peptides are found in all forms of life and demonstrate a pivotal role in the innate immune system. Many antimicrobial peptides are evolutionarily conserved, with limited propensity for resistance. Additionally, chemical modifications to the peptide backbone can be used to improve biological activity and stability and reduce toxicity. This review details the therapeutic potential of peptide-based antimicrobials, as well as the challenges needed to overcome in order for clinical translation. We explore the proposed mechanisms of activity, design of synthetic biomimics, and how this novel class of antimicrobial compound may address the need for effective antibiotics. Finally, we discuss commercially available peptide-based antimicrobials and antimicrobial peptides in clinical trials.

摘要

抗菌药物耐药性是一个多方面的危机,对全球健康构成严重威胁。传统的抗生素研发途径已经枯竭,促使人们研究替代抗菌策略。受自然启发,抗菌肽因其作为临床应用的潜力而受到广泛关注,因为它们具有优于传统抗生素的显著优势。抗菌肽存在于所有生命形式中,在先天免疫系统中发挥着关键作用。许多抗菌肽在进化上是保守的,耐药性的倾向有限。此外,可以对肽骨架进行化学修饰,以提高生物活性和稳定性,降低毒性。这篇综述详细介绍了基于肽的抗菌药物的治疗潜力,以及为实现临床转化而需要克服的挑战。我们探讨了活性的拟议机制、合成仿生物的设计,以及这一新型抗菌化合物如何满足对抗菌药物的有效需求。最后,我们讨论了临床上可获得的基于肽的抗菌药物和处于临床试验阶段的抗菌肽。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7504/7582481/fec9ac9f5979/ijms-21-07047-g003a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7504/7582481/00f4c15373c6/ijms-21-07047-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7504/7582481/4e0372311f0f/ijms-21-07047-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7504/7582481/fec9ac9f5979/ijms-21-07047-g003a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7504/7582481/00f4c15373c6/ijms-21-07047-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7504/7582481/4e0372311f0f/ijms-21-07047-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7504/7582481/fec9ac9f5979/ijms-21-07047-g003a.jpg

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Antimicrobial Peptides: Mechanisms, Applications, and Therapeutic Potential.

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[2]
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[4]
Expansion of the antibacterial spectrum of symmetrical amino acid-paired antifungal peptides through structural optimization.

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[5]
Modulating Antimicrobial Activity and Structure of the Peptide Esc(1-21) via Site-Specific Isopeptide Bond Formation.

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[6]
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[7]
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[8]
Anti-biofilm peptides can rescue fluconazole and amphotericin B efficacies against Candida albicans.

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[9]
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Iran J Microbiol. 2025-6

[10]
Ruthenium-quercetin coordinated nanotherapeutics with macrophage polarization regulation to rapidly promote bacterial-infected wound healing.

Mater Today Bio. 2025-6-20

本文引用的文献

[1]
The unusual structure of Ruminococcin C1 antimicrobial peptide confers clinical properties.

Proc Natl Acad Sci U S A. 2020-7-27

[2]
The value of antimicrobial peptides in the age of resistance.

Lancet Infect Dis. 2020-7-9

[3]
Antimicrobial Resistance in ESKAPE Pathogens.

Clin Microbiol Rev. 2020-6-17

[4]
Are Antimicrobial Peptide Dendrimers an Escape from ESKAPE?

Adv Wound Care (New Rochelle). 2020-5-19

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Biomed Res Int. 2020-3-10

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Antifungal Peptides as Therapeutic Agents.

Front Cell Infect Microbiol. 2020

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Synergy Pattern of Short Cationic Antimicrobial Peptides Against Multidrug-Resistant .

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Nat Rev Microbiol. 2019-11-19

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