Department of Pathology and Microbiology, College of Medicine, University of Nebraska Medical Center, Omaha, Nebraska 68198, United States.
Department of Internal Medicine, College of Medicine, University of Nebraska Medical Center, Omaha, Nebraska 68198, United States.
ACS Infect Dis. 2023 Apr 14;9(4):716-738. doi: 10.1021/acsinfecdis.3c00050. Epub 2023 Mar 30.
The treatment of infections is becoming more difficult due to emerging resistance of pathogens to existing drugs. As such, alternative druggable targets, particularly those that are essential for microbe viability and thus make it harder to develop resistance, are desperately needed. In turn, once identified, safe and effective agents that disrupt these targets must be developed. Microbial acquisition and use of iron is a promising novel target for antimicrobial drug development. In this Review we look at the various facets of iron metabolism critical to human infection with pathogenic microbes and the various ways in which it can be targeted, altered, disrupted, and taken advantage of to halt or eliminate microbial infections. Although a variety of agents will be touched upon, the primary focus will be on the potential use of one or more gallium complexes as a new class of antimicrobial agents. and data on the activity of gallium complexes against a variety of pathogens including ESKAPE pathogens, mycobacteria, emerging viruses, and fungi will be discussed in detail, as well as pharmacokinetics, novel formulations and delivery approaches, and early human clinical results.
由于病原体对现有药物的耐药性不断出现,感染的治疗变得更加困难。因此,迫切需要替代的可成药靶点,特别是那些对微生物生存至关重要的靶点,因为这些靶点更难产生耐药性。反过来,一旦确定了这些靶点,就必须开发出安全有效的能够破坏这些靶点的药物。微生物获取和利用铁是开发抗菌药物的一个有前途的新靶点。在这篇综述中,我们探讨了铁代谢对人类感染致病微生物至关重要的各个方面,以及可以针对这些方面进行靶向、改变、干扰和利用的各种方法,以阻止或消除微生物感染。虽然将涉及各种药物,但主要重点将放在一种或多种镓配合物作为一类新的抗菌药物的潜在用途上。将详细讨论镓配合物对各种病原体(包括 ESKAPE 病原体、分枝杆菌、新兴病毒和真菌)的活性数据,以及药代动力学、新型制剂和给药方法,以及早期人体临床结果。