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应对产金属β-内酰胺酶革兰氏阴性菌感染的当前治疗格局:存在哪些局限性?

Navigating the Current Treatment Landscape of Metallo-β-Lactamase-Producing Gram-Negative Infections: What are the Limitations?

作者信息

Grabein Beatrice, Arhin Francis F, Daikos George L, Moore Luke S P, Balaji V, Baillon-Plot Nathalie

机构信息

LMU Hospital Munich, Munich, Germany.

Pfizer, Kirkland, Canada.

出版信息

Infect Dis Ther. 2024 Nov;13(11):2423-2447. doi: 10.1007/s40121-024-01044-8. Epub 2024 Oct 1.

DOI:10.1007/s40121-024-01044-8
PMID:39352652
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11499561/
Abstract

The spread of carbapenemase-producing gram-negative pathogens, especially those producing metallo-β-lactamases (MBLs), has become a major health concern. MBLs are molecularly the most diverse carbapenemases, produced by a wide spectrum of gram-negative organisms, including the Enterobacterales, Pseudomonas spp., Acinetobacter baumannii, and Stenotrophomonas maltophilia, and can hydrolyze most β-lactams using metal ion cofactors in their active sites. Over the years, the prevalence of MBL-carrying isolates has increased globally, particularly in Asia. MBL infections are associated with adverse clinical outcomes including longer length of hospital stay, ICU admission, and increased mortality across the globe. The optimal treatment for MBL infections not only depends on the pathogen but also on the underlying resistance mechanisms. Currently, there are only few drugs or drug combinations that can efficiently offset MBL-mediated resistance, which makes the treatment of MBL infections challenging. The rising concern of MBLs along with the limited treatment options has led to the need and development of drugs that are specifically targeted towards MBLs. This review discusses the prevalence of MBLs, their clinical impact, and the current treatment options for MBL infections and their limitations. Furthermore, this review will discuss agents currently in the pipeline for treatment of MBL infections.

摘要

产碳青霉烯酶革兰氏阴性病原体的传播,尤其是那些产生金属β-内酰胺酶(MBL)的病原体,已成为一个主要的健康问题。MBL在分子层面上是种类最多样化的碳青霉烯酶,由多种革兰氏阴性菌产生,包括肠杆菌科细菌、假单胞菌属、鲍曼不动杆菌和嗜麦芽窄食单胞菌,并且可以利用其活性位点中的金属离子辅因子水解大多数β-内酰胺类抗生素。多年来,携带MBL的分离株在全球范围内的流行率有所上升,尤其是在亚洲。MBL感染与不良临床结局相关,包括全球范围内更长的住院时间、入住重症监护病房以及死亡率增加。MBL感染的最佳治疗不仅取决于病原体,还取决于潜在的耐药机制。目前,只有少数药物或药物组合能够有效抵消MBL介导的耐药性,这使得MBL感染的治疗具有挑战性。对MBL的日益关注以及有限的治疗选择导致了针对MBL的特异性药物的需求和开发。本综述讨论了MBL的流行情况、它们的临床影响、MBL感染的当前治疗选择及其局限性。此外,本综述还将讨论目前正在研发的用于治疗MBL感染的药物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/26f6/11499561/feb10aae14fa/40121_2024_1044_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/26f6/11499561/feb10aae14fa/40121_2024_1044_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/26f6/11499561/feb10aae14fa/40121_2024_1044_Fig1_HTML.jpg

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