Roque-Borda Cesar Augusto, Primo Laura Maria Duran Gleriani, Medina-Alarcón Kaila Petronila, Campos Isabella C, Nascimento Camila de Fátima, Saraiva Mauro M S, Berchieri Junior Angelo, Fusco-Almeida Ana Marisa, Mendes-Giannini Maria José Soares, Perdigão João, Pavan Fernando Rogério, Albericio Fernando
Department of Biological Sciences, School of Pharmaceutical Sciences, Universidade Estadual Paulista (UNESP), Araraquara, Sao Paulo, 14800-903, Brazil.
iMed.ULisboa-Institute for Medicines Research, Faculty of Pharmacy, University of Lisbon, Lisbon, 1649004, Portugal.
Adv Sci (Weinh). 2025 Jan;12(1):e2410893. doi: 10.1002/advs.202410893. Epub 2024 Nov 12.
Polymicrobial biofilms adhere to surfaces and enhance pathogen resistance to conventional treatments, significantly contributing to chronic infections in the respiratory tract, oral cavity, chronic wounds, and on medical devices. This review examines antimicrobial peptides (AMPs) as a promising alternative to traditional antibiotics for treating biofilm-associated infections. AMPs, which can be produced as part of the innate immune response or synthesized therapeutically, have broad-spectrum antimicrobial activity, often disrupting microbial cell membranes and causing cell death. Many specifically target negatively charged bacterial membranes, unlike host cell membranes. Research shows AMPs effectively inhibit and disrupt polymicrobial biofilms and can enhance conventional antibiotics' efficacy. Preclinical and clinical research is advancing, with animal studies and clinical trials showing promise against multidrug-resistant bacteria and fungi. Numerous patents indicate increasing interest in AMPs. However, challenges such as peptide stability, potential cytotoxicity, and high production costs must be addressed. Ongoing research focuses on optimizing AMP structures, enhancing stability, and developing cost-effective production methods. In summary, AMPs offer a novel approach to combating biofilm-associated infections, with their unique mechanisms and synergistic potential with existing antibiotics positioning them as promising candidates for future treatments.
多种微生物形成的生物膜会附着在表面,并增强病原体对传统治疗的抵抗力,这在很大程度上导致了呼吸道、口腔、慢性伤口以及医疗器械上的慢性感染。本综述探讨了抗菌肽(AMPs)作为治疗生物膜相关感染的一种有前景的传统抗生素替代物。抗菌肽可作为先天性免疫反应的一部分产生,也可通过治疗性合成,具有广谱抗菌活性,通常会破坏微生物细胞膜并导致细胞死亡。与宿主细胞膜不同,许多抗菌肽特异性靶向带负电荷的细菌膜。研究表明,抗菌肽能有效抑制和破坏多种微生物形成的生物膜,并可增强传统抗生素的疗效。临床前和临床研究正在推进,动物研究和临床试验显示出对抗多重耐药细菌和真菌的前景。众多专利表明人们对抗菌肽的兴趣与日俱增。然而,必须解决诸如肽稳定性、潜在细胞毒性和高生产成本等挑战。正在进行的研究集中在优化抗菌肽结构、增强稳定性以及开发具有成本效益的生产方法。总之,抗菌肽提供了一种对抗生物膜相关感染的新方法,其独特的作用机制以及与现有抗生素的协同潜力使其成为未来治疗的有希望的候选者。