Cefiderocol: a novel siderophore cephalosporin

被引:62
作者
Choi, Justin J. [1 ]
McCarthy, Matthew W. [2 ]
机构
[1] Weill Cornell Med Coll, Dept Med, New York, NY USA
[2] New York Presbyterian Hosp, Div Gen Internal Med, New York, NY USA
关键词
Siderophore; carbapenemase; resistance; Gram negative; urinary tract infection; NEGATIVE BACTERIAL-INFECTIONS; KLEBSIELLA-PNEUMONIAE; IMIPENEM RESISTANCE; EMERGENCE; SPREAD; AGENTS; DELHI; NDM-1;
D O I
10.1080/13543784.2018.1426745
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Introduction: The emergence of multidrug-resistant bacterial pathogens has led to a global public health emergency and novel therapeutic options and drug-delivery systems are urgently needed. Cefiderocol is a siderophore cephalosporin antibiotic that has recently been developed to combat a variety of bacterial pathogens, including beta-lactam- and carbapenem-resistant organisms. Areas covered: This paper provides an overview of the mutational and plasmid-mediated mechanisms of beta-lactam and carbapenem resistance, the biochemical pathways of siderophores in bacterial iron metabolism, and how cefiderocol may be able to provide better targeted antimicrobial therapy that escape these drug-resistant mechanisms. We also explore the pharmacokinetics of this new compound as well as results from preclinical and clinical studies. Expert opinion: There is an urgent need for novel antimicrobial agents to address the emergence of multidrug-resistant pathogens, which are an increasing cause of morbidity and mortality worldwide. Our understanding of multidrug-resistance and bacterial biochemical pathways continues to expand, and the development of cefiderocol specifically targeting siderophore-mediated iron transport shows potential in escaping mechanisms of drug resistance. Cefiderocol, which demonstrates a favorable side effect profile, has the potential to become first-line therapy for our most aggressive and lethal multidrug-resistant Gram-negative pathogens.
引用
收藏
页码:193 / 197
页数:5
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