Center for Anti-Infective Research and Development, Hartford Hospital, Hartford, Connecticut, USA.
Department of Intensive Care Medicine, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
Pharmacotherapy. 2024 Aug;44(8):658-674. doi: 10.1002/phar.2950. Epub 2024 Jul 1.
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.
由于β-内酰胺酶的不断进化导致经典β-内酰胺(BL)抗生素的活性降低,抗生素耐药性已成为全球性威胁。最近的抗生素发现和开发工作已经产生了针对扩展谱β-内酰胺酶以及产肺炎克雷伯菌碳青霉烯酶(KPC)的碳青霉烯类耐药菌(CRO)的β-内酰胺酶抑制剂(BLIs)。然而,仍然缺乏针对金属β-内酰胺酶(MBL)的药物,这些酶能够有效地水解碳青霉烯类药物,以及经常存在于碳青霉烯类耐药鲍曼不动杆菌中的耐甲氧西林青霉素酶(OXA)。本综述旨在提供有关目前可用于治疗 CRO 的 BL/BLI 治疗选择以及处于后期开发阶段的针对各种β-内酰胺酶(包括 MBL 和 OXA 酶)的药物的微生物学、药理学和临床数据的概述。