Watkins Richard R, Lemonovich Tracy L, Vila Alejandro J, Bonomo Robert A
Division of Infectious Diseases, Northeast Ohio Medical University, Rootstown, Ohio, USA.
Division of Infectious Diseases, MetroHealth Medical Center, Cleveland, Ohio, USA.
J Infect Dis. 2025 Aug 14;232(2):278-284. doi: 10.1093/infdis/jiaf203.
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.
抗菌药物耐药性的持续传播迫切需要新型抗生素,尤其是针对多重耐药(MDR)革兰氏阴性病原体的抗生素。他尼硼巴坦(以前称为VNRX-5133)是一种新型双环硼酸酯β-内酰胺酶抑制剂,对安布勒A、B、C和D类酶具有强效、选择性和直接抑制活性,包括丝氨酸和金属β-内酰胺酶。他尼硼巴坦的抑制谱比目前任何其他β-内酰胺酶抑制剂都更广。头孢吡肟与他尼硼巴坦的联合用药正处于临床开发后期。研究人员正在研究头孢吡肟-他尼硼巴坦对革兰氏阴性病原体的活性,包括肠杆菌科细菌,如具有特征性碳青霉烯耐药机制的耐碳青霉烯肺炎克雷伯菌和多重耐药铜绿假单胞菌。在这篇综述中,我们讨论了促成头孢吡肟-他尼硼巴坦开发的药物化学进展、药代动力学和药效学、抗菌活性谱、临床潜在用途以及耐药机制。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确切适用范围。