Department of Chemistry, Aarhus University, Aarhus C, 8000, Denmark.
Department of Clinical Medicine, Aarhus University, Aarhus N, 8200, Denmark.
Adv Sci (Weinh). 2023 Aug;10(23):e2301340. doi: 10.1002/advs.202301340. Epub 2023 Jun 8.
The treatment of implant-associated bacterial infections and biofilms is an urgent medical need and a grand challenge because biofilms protect bacteria from the immune system and harbor antibiotic-tolerant persister cells. This need is addressed herein through an engineering of antibody-drug conjugates (ADCs) that contain an anti-neoplastic drug mitomycin C, which is also a potent antimicrobial against biofilms. The ADCs designed herein release the conjugated drug without cell entry, via a novel mechanism of drug release which likely involves an interaction of ADC with the thiols on the bacterial cell surface. ADCs targeted toward bacteria are superior by the afforded antimicrobial effects compared to the non-specific counterpart, in suspension and within biofilms, in vitro, and in an implant-associated murine osteomyelitis model in vivo. The results are important in developing ADC for a new area of application with a significant translational potential, and in addressing an urgent medical need of designing a treatment of bacterial biofilms.
治疗与植入物相关的细菌感染和生物膜是一项紧迫的医学需求和重大挑战,因为生物膜可以保护细菌免受免疫系统的攻击,并藏匿对抗生素具有耐受性的休眠细胞。通过工程设计抗体药物偶联物(ADC)来解决这一需求,ADC 中包含抗肿瘤药物丝裂霉素 C,它也是一种对抗生物膜的有效抗菌药物。本文设计的 ADC 可以通过一种新的药物释放机制在不进入细胞的情况下释放结合药物,这种机制可能涉及 ADC 与细菌细胞表面上的巯基相互作用。与非特异性 ADC 相比,针对细菌的 ADC 在体外的悬液中和生物膜内具有更好的抗菌效果,并且在体内植入物相关的骨髓炎模型中也具有更好的效果。这些结果对于开发用于具有重要转化潜力的新应用领域的 ADC 以及设计治疗细菌生物膜的方法具有重要意义。