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

IF 4.7 3区 医学 Q1 INFECTIOUS DISEASES
Infectious Diseases and Therapy Pub Date : 2024-11-01 Epub Date: 2024-10-01 DOI:10.1007/s40121-024-01044-8
Beatrice Grabein, Francis F Arhin, George L Daikos, Luke S P Moore, V Balaji, Nathalie Baillon-Plot
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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.

引导产生金属-β-乳酰胺酶的革兰氏阴性菌感染的现有治疗方案:有哪些局限性?
产生碳青霉烯酶的革兰氏阴性病原体,尤其是产生金属-β-内酰胺酶(MBLs)的病原体的传播已成为一个重大的健康问题。MBLs 是分子上最多样化的碳青霉烯酶,由多种革兰氏阴性菌产生,包括肠杆菌属、假单胞菌属、鲍曼不动杆菌属和嗜麦芽气单胞菌属,可利用其活性位点中的金属离子辅助因子水解大多数 β-内酰胺类药物。多年来,全球,尤其是亚洲,携带 MBL 的分离菌株的流行率有所上升。在全球范围内,MBL 感染与不良临床结果有关,包括住院时间延长、入住重症监护室和死亡率上升。治疗 MBL 感染的最佳方法不仅取决于病原体,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。由于人们对 MBL 的关注度不断提高,而治疗方案却十分有限,因此需要开发专门针对 MBL 的药物。本综述将讨论 MBL 的流行情况、其临床影响、MBL 感染的现有治疗方案及其局限性。此外,本综述还将讨论目前正在研发的治疗 MBL 感染的药物。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Infectious Diseases and Therapy
Infectious Diseases and Therapy Medicine-Microbiology (medical)
CiteScore
8.60
自引率
1.90%
发文量
136
审稿时长
6 weeks
期刊介绍: Infectious Diseases and Therapy is an international, open access, peer-reviewed, rapid publication journal dedicated to the publication of high-quality clinical (all phases), observational, real-world, and health outcomes research around the discovery, development, and use of infectious disease therapies and interventions, including vaccines and devices. Studies relating to diagnostic products and diagnosis, pharmacoeconomics, public health, epidemiology, quality of life, and patient care, management, and education are also encouraged. Areas of focus include, but are not limited to, bacterial and fungal infections, viral infections (including HIV/AIDS and hepatitis), parasitological diseases, tuberculosis and other mycobacterial diseases, vaccinations and other interventions, and drug-resistance, chronic infections, epidemiology and tropical, emergent, pediatric, dermal and sexually-transmitted diseases.
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