Evolving resistance landscape in gram-negative pathogens: An update on β-lactam and β-lactam-inhibitor treatment combinations for carbapenem-resistant organisms.

IF 2.9 3区 医学 Q2 PHARMACOLOGY & PHARMACY
Pharmacotherapy Pub Date : 2024-08-01 Epub Date: 2024-07-01 DOI:10.1002/phar.2950
Christina Koenig, Joseph L Kuti
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引用次数: 0

Abstract

Antibiotic resistance has become a global threat as it is continuously growing due to the evolution of β-lactamases diminishing the activity of classic β-lactam (BL) antibiotics. Recent antibiotic discovery and development efforts have led to the availability of β-lactamase inhibitors (BLIs) with activity against extended-spectrum β-lactamases as well as Klebsiella pneumoniae carbapenemase (KPC)-producing carbapenem-resistant organisms (CRO). Nevertheless, there is still a lack of drugs that target metallo-β-lactamases (MBL), which hydrolyze carbapenems efficiently, and oxacillinases (OXA) often present in carbapenem-resistant Acinetobacter baumannii. This review aims to provide a snapshot of microbiology, pharmacology, and clinical data for currently available BL/BLI treatment options as well as agents in late stage development for CRO harboring various β-lactamases including MBL and OXA-enzymes.

革兰氏阴性病原体耐药性的演变:针对耐碳青霉烯类病菌的β-内酰胺和β-内酰胺抑制剂治疗组合的最新进展。
由于β-内酰胺酶的进化削弱了传统β-内酰胺(BL)抗生素的活性,抗生素耐药性不断增加,已成为一种全球性威胁。最近的抗生素发现和开发工作促使β-内酰胺酶抑制剂(BLIs)的出现,它们对广谱β-内酰胺酶以及产生碳青霉烯耐药菌(CRO)的肺炎克雷伯菌碳青霉烯酶(KPC)具有活性。然而,目前仍缺乏针对金属-β-内酰胺酶(MBL)和氧青霉素酶(OXA)的药物,金属-β-内酰胺酶能有效水解碳青霉烯类药物,而氧青霉素酶通常存在于耐碳青霉烯类鲍曼不动杆菌中。本综述旨在简要介绍目前可用的 BL/BLI 治疗方案的微生物学、药理学和临床数据,以及针对携带各种 β-内酰胺酶(包括 MBL 和 OXA 酶)的 CRO 的处于后期开发阶段的药物。
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
Pharmacotherapy
Pharmacotherapy 医学-药学
CiteScore
7.80
自引率
2.40%
发文量
93
审稿时长
4-8 weeks
期刊介绍: Pharmacotherapy is devoted to publication of original research articles on all aspects of human pharmacology and review articles on drugs and drug therapy. The Editors and Editorial Board invite original research reports on pharmacokinetic, bioavailability, and drug interaction studies, clinical trials, investigations of specific pharmacological properties of drugs, and related topics.
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