Department of Environmental and Prevention Sciences, University of Ferrara, 44121 Ferrara, Italy.
Faculty of Chemistry, University of Wrocław, 50-383 Wrocław, Poland.
Molecules. 2022 Jul 18;27(14):4584. doi: 10.3390/molecules27144584.
The emergence of antimicrobial-resistant infections is still a major concern for public health worldwide. The number of pathogenic microorganisms capable of resisting common therapeutic treatments are constantly increasing, highlighting the need of innovative and more effective drugs. This phenomenon is strictly connected to the rapid metabolism of microorganisms: due to the huge number of mutations that can occur in a relatively short time, a colony can "adapt" to the pharmacological treatment with the evolution of new resistant species. However, the shortage of available antimicrobial drugs in clinical use is also caused by the high costs involved in developing and marketing new drugs without an adequate guarantee of an economic return; therefore, the pharmaceutical companies have reduced their investments in this area. The use of antimicrobial peptides (AMPs) represents a promising strategy for the design of new therapeutic agents. AMPs act as immune defense mediators of the host organism and show a poor ability to induce antimicrobial resistance, coupled with other advantages such as a broad spectrum of activity, not excessive synthetic costs and low toxicity of both the peptide itself and its own metabolites. It is also important to underline that many antimicrobial peptides, due to their inclination to attack cell membranes, have additional biological activities, such as, for example, as anti-cancer drugs. Unfortunately, they usually undergo rapid degradation by proteolytic enzymes and are characterized by poor bioavailability, preventing their extensive clinical use and landing on the pharmaceutical market. This review is focused on the strength and weak points of antimicrobial peptides as therapeutic agents. We give an overview on the AMPs already employed in clinical practice, which are examples of successful strategies aimed at overcoming the main drawbacks of peptide-based drugs. The review deepens the most promising strategies to design modified antimicrobial peptides with higher proteolytic stability with the purpose of giving a comprehensive summary of the commonly employed approaches to evaluate and optimize the peptide potentialities.
抗微生物药物耐药性感染的出现仍然是全球公共卫生的主要关注点。能够抵抗常见治疗方法的致病微生物的数量不断增加,这突出表明需要创新和更有效的药物。这种现象与微生物的快速代谢密切相关:由于在相对较短的时间内可能发生大量突变,一个菌落可以通过进化出新的耐药物种来“适应”药理治疗。然而,临床上可用的抗微生物药物短缺也是由于开发和销售新药物的高成本,而没有足够的经济回报保证;因此,制药公司减少了在这一领域的投资。抗菌肽 (AMPs) 的使用代表了设计新治疗剂的有前途的策略。AMPs 作为宿主生物体的免疫防御介质发挥作用,并且显示出诱导抗微生物耐药性的能力较差,此外还具有其他优点,例如广谱活性、不过度的合成成本以及肽本身及其自身代谢物的低毒性。同样重要的是要强调的是,由于许多抗菌肽倾向于攻击细胞膜,因此具有额外的生物学活性,例如作为抗癌药物。不幸的是,它们通常会被蛋白酶迅速降解,并且具有较差的生物利用度,这阻止了它们的广泛临床应用和在制药市场上的应用。这篇综述重点介绍了作为治疗剂的抗菌肽的优势和弱点。我们概述了已经在临床实践中使用的 AMPs,它们是旨在克服基于肽的药物主要缺点的成功策略的范例。综述深入探讨了设计具有更高蛋白酶稳定性的改良抗菌肽的最有前途的策略,目的是全面总结评估和优化肽潜力的常用方法。