Department of Internal Medicine, Northeast Ohio Medical University Rootstown, OH, USA ; Division of Infectious Diseases, Akron General Medical Center Akron, OH, USA.
Research Service, Louis Stokes Cleveland Department of Veterans Affairs Medical Center Cleveland, OH, USA ; Department of Medicine, Case Western Reserve University Cleveland, OH, USA.
Front Microbiol. 2013 Dec 24;4:392. doi: 10.3389/fmicb.2013.00392.
The increasing incidence and prevalence of multi-drug resistance (MDR) among contemporary Gram-negative bacteria represents a significant threat to human health. Since their discovery, β-lactam antibiotics have been a major component of the armamentarium against these serious pathogens. Unfortunately, a wide range of β-lactamase enzymes have emerged that are capable of inactivating these powerful drugs. In the past 30 years, a major advancement in the battle against microbes has been the development of β-lactamase inhibitors, which restore the efficacy of β-lactam antibiotics (e.g., ampicillin/sulbactam, amoxicillin/clavulanate, ticarcillin/clavulanate, and piperacillin/tazobactam). Unfortunately, many newly discovered β-lactamases are not inactivated by currently available inhibitors. Is there hope? For the first time in many years, we can anticipate the development and introduction into clinical practice of novel inhibitors. Although these inhibitors may still not be effective for all β-lactamases, their introduction is still welcome. This review focuses on the novel β-lactamase inhibitors that are closest to being introduced in the clinic.
当代革兰氏阴性菌中多药耐药(MDR)的发病率和患病率不断上升,这对人类健康构成了重大威胁。自发现以来,β-内酰胺类抗生素一直是对抗这些严重病原体的主要武器。不幸的是,出现了多种能够使这些强效药物失活的β-内酰胺酶。在过去的 30 年中,对抗微生物的一个主要进展是β-内酰胺酶抑制剂的开发,它恢复了β-内酰胺类抗生素的疗效(例如,氨苄西林/舒巴坦、阿莫西林/克拉维酸、替卡西林/克拉维酸和哌拉西林/他唑巴坦)。不幸的是,许多新发现的β-内酰胺酶不受现有抑制剂的抑制。有希望吗?多年来,我们首次可以预期新型抑制剂的开发和引入临床实践。尽管这些抑制剂可能对所有β-内酰胺酶仍然无效,但它们的引入仍然受到欢迎。这篇综述重点介绍了最接近引入临床的新型β-内酰胺酶抑制剂。