Cefepime-Taniborbactam-a Novel Combination Therapy for Multidrug-Resistant Pathogens.

Richard R Watkins,Tracy L Lemonovich,Alejandro J Vila,Robert A Bonomo
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Abstract

The ongoing spread of antimicrobial resistance has generated an urgent need for new antibiotics, especially against multidrug-resistant (MDR) gram-negative pathogens. Taniborbactam (previously VNRX-5133) is a novel bicyclic boronate β-lactamase inhibitor with potent, selective, and direct inhibitory activity against Ambler class A, B, C, and D enzymes, including serine and metallo-β-lactamases. Taniborbactam has a broader spectrum of inhibition than any other current β-lactamase inhibitor. The combination of cefepime with taniborbactam is in advanced clinical development. Investigators are studying the activity of cefepime-taniborbactam against gram-negative pathogens, including Enterobacterales species like carbapenem-resistant Klebsiella pneumoniae and MDR Pseudomonas aeruginosa with characterized carbapenem resistance mechanisms. In this review, we discuss the advances in medicinal chemistry that led to the development of cefepime-taniborbactam, the pharmacokinetics and pharmacodynamics, the antimicrobial spectrum of activity, potential uses in the clinic, and mechanisms of resistance. We propose future clinical scenarios to better explore the precise niche of this novel inhibitor combination.
头孢吡肟-塔尼波巴坦-一种治疗多重耐药病原体的新型联合疗法。
抗菌素耐药性的持续蔓延导致迫切需要新的抗生素,特别是针对多重耐药(MDR)革兰氏阴性病原体。Taniborbactam(以前的VNRX-5133)是一种新型的双环硼酸β-内酰胺酶抑制剂,对Ambler a、B、C和D类酶具有有效的、选择性的和直接的抑制活性,包括丝氨酸和金属β-内酰胺酶。Taniborbactam具有比目前任何其他β-内酰胺酶抑制剂更广泛的抑制谱。头孢吡肟联合坦尼波巴坦的临床研究处于后期阶段。研究人员正在研究头孢吡肟-taniborbactam对革兰氏阴性病原体的活性,包括碳青霉烯耐药肺炎克雷伯菌和耐多药铜绿假单胞菌等具有碳青霉烯耐药机制的肠杆菌。本文综述了头孢吡肟-他尼波巴坦在药物化学方面的研究进展、药代动力学和药效学、抗菌活性谱、临床应用前景和耐药机制。我们提出了未来的临床方案,以更好地探索这种新型抑制剂组合的精确利基。
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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