Ridyard Kylen E, Overhage Joerg
Department of Health Sciences, Carleton University, Ottawa, ON K1S 5B6, Canada.
Antibiotics (Basel). 2021 May 29;10(6):650. doi: 10.3390/antibiotics10060650.
The rise in antimicrobial resistant bacteria threatens the current methods utilized to treat bacterial infections. The development of novel therapeutic agents is crucial in avoiding a post-antibiotic era and the associated deaths from antibiotic resistant pathogens. The human antimicrobial peptide LL-37 has been considered as a potential alternative to conventional antibiotics as it displays broad spectrum antibacterial and anti-biofilm activities as well as immunomodulatory functions. While LL-37 has shown promising results, it has yet to receive regulatory approval as a peptide antibiotic. Despite the strong antimicrobial properties, LL-37 has several limitations including high cost, lower activity in physiological environments, susceptibility to proteolytic degradation, and high toxicity to human cells. This review will discuss the challenges associated with making LL-37 into a viable antibiotic treatment option, with a focus on antimicrobial resistance and cross-resistance as well as adaptive responses to sub-inhibitory concentrations of the peptide. The possible methods to overcome these challenges, including immobilization techniques, LL-37 delivery systems, the development of LL-37 derivatives, and synergistic combinations will also be considered. Herein, we describe how combination therapy and structural modifications to the sequence, helicity, hydrophobicity, charge, and configuration of LL-37 could optimize the antimicrobial and anti-biofilm activities of LL-37 for future clinical use.
抗菌耐药细菌的增加威胁到目前用于治疗细菌感染的方法。开发新型治疗药物对于避免进入后抗生素时代以及避免因抗生素耐药病原体导致的相关死亡至关重要。人抗菌肽LL-37被认为是传统抗生素的一种潜在替代品,因为它具有广谱抗菌和抗生物膜活性以及免疫调节功能。虽然LL-37已显示出有前景的结果,但它尚未获得作为肽类抗生素的监管批准。尽管LL-37具有强大的抗菌特性,但它有几个局限性,包括成本高、在生理环境中活性较低、易受蛋白水解降解以及对人类细胞毒性高。本综述将讨论将LL-37转化为可行的抗生素治疗选择所面临的挑战,重点关注抗菌耐药性和交叉耐药性以及对亚抑制浓度肽的适应性反应。还将考虑克服这些挑战的可能方法,包括固定化技术、LL-37递送系统、LL-37衍生物的开发以及协同组合。在此,我们描述了联合疗法以及对LL-37的序列、螺旋度、疏水性、电荷和构象进行结构修饰如何能够优化LL-37的抗菌和抗生物膜活性以供未来临床使用。