Department of Immunology and Infectious Diseases, Harvard T.H. Chan School of Public Health, Boston, Massachusetts 02115, United States.
Bioengineering Laboratory, Department of Chemical and Biological Engineering, Monash University, Clayton, VIC 3800, Australia.
ACS Nano. 2024 Jan 30;18(4):2564-2577. doi: 10.1021/acsnano.3c11045. Epub 2024 Jan 16.
Antibiotic resistance is a major driver of morbidity and mortality worldwide, necessitating alternatives. Due to their mechanism of action, bacteriophages, endolysins, and antimicrobial peptides (coined herein as nonantibiotic antibacterials, NAA) have risen to tackle this problem and led to paradigms in treating antibiotic-resistant bacterial infections. However, their clinical applications remain challenging and have been seriously hampered by cytotoxicity, instability, weak bioactivity, low on-target bioavailability, high pro-inflammatory responses, shorter half-life, and circulatory properties. Hence, to transit preclinical phases and beyond, it has become imperative to radically engineer these alternatives into innovative and revolutionary therapeutics to overcome recalcitrant infections. This perspective highlights the promise of these agents, their limitations, promising designs, nanotechnology, and delivery approaches that can be harnessed to transform these agents. Finally, I provide an outlook on the remaining challenges that need to be tackled for their widespread clinical administration.
抗生素耐药性是全球发病率和死亡率的主要驱动因素,因此需要寻找替代品。由于其作用机制,噬菌体、内溶素和抗菌肽(本文称为非抗生素抗菌剂,NAA)已被用于解决这一问题,并引领了治疗抗生素耐药性细菌感染的新范式。然而,它们的临床应用仍然具有挑战性,并且一直受到细胞毒性、不稳定性、生物活性弱、靶标生物利用度低、高炎症反应、半衰期短和循环特性等因素的严重阻碍。因此,为了实现从临床前阶段到更深入的研究,必须将这些替代品彻底设计为创新和革命性的治疗方法,以克服耐药性感染。本文观点强调了这些药物的潜力、局限性、有前途的设计、纳米技术和给药方法,这些都可以被利用来改变这些药物。最后,我对广泛临床应用所需解决的剩余挑战进行了展望。