Servicio de Microbiología, Instituto de Investigación Biomédica de A Coruña (INIBIC-CICA), Complejo Hospitalario Universitario A Coruña (CHUAC), As Xubias 84, 15006 A Coruña, Spain.
Int J Mol Sci. 2020 Dec 6;21(23):9308. doi: 10.3390/ijms21239308.
Carbapenem resistance is a major global health problem that seriously compromises the treatment of infections caused by nosocomial pathogens. Resistance to carbapenems mainly occurs via the production of carbapenemases, such as VIM, IMP, NDM, KPC and OXA, among others. Preclinical and clinical trials are currently underway to test a new generation of promising inhibitors, together with the recently approved avibactam, relebactam and vaborbactam. This review summarizes the main, most promising carbapenemase inhibitors synthesized to date, as well as their spectrum of activity and current stage of development. We particularly focus on β-lactam/β-lactamase inhibitor combinations that could potentially be used to treat infections caused by carbapenemase-producer pathogens of critical priority. The emergence of these new combinations represents a step forward in the fight against antimicrobial resistance, especially in regard to metallo-β-lactamases and carbapenem-hydrolysing class D β-lactamases, not currently inhibited by any clinically approved inhibitor.
碳青霉烯类耐药性是一个全球性的主要健康问题,严重影响了医院获得性病原体感染的治疗。碳青霉烯类耐药性主要通过产生碳青霉烯酶,如 VIM、IMP、NDM、KPC 和 OXA 等来实现。目前正在进行临床前和临床试验,以测试新一代有前途的抑制剂,以及最近批准的阿维巴坦、雷利巴坦和沃巴坦。这篇综述总结了迄今为止合成的主要的、最有前途的碳青霉烯酶抑制剂,以及它们的活性谱和当前的开发阶段。我们特别关注β-内酰胺/β-内酰胺酶抑制剂组合,这些组合可能有潜力用于治疗具有关键优先级的碳青霉烯酶产生病原体引起的感染。这些新组合的出现代表着在对抗抗菌药物耐药性方面向前迈进了一步,特别是在针对目前没有任何临床批准的抑制剂抑制的金属β-内酰胺酶和碳青霉烯水解类 Dβ-内酰胺酶方面。