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用于治疗严重革兰氏阳性菌感染的新型抗菌剂。

Novel antibacterial agents for the treatment of serious Gram-positive infections.

作者信息

Abbanat Darren, Macielag Mark, Bush Karen

机构信息

Johnson & Johnson Research & Development, 1000 Route 202, Raritan, NJ 08869, USA.

出版信息

Expert Opin Investig Drugs. 2003 Mar;12(3):379-99. doi: 10.1517/13543784.12.3.379.

Abstract

With the continuing development of clinical drug resistance among bacteria and the advent of resistance to the recently released agents quinupristin-dalfopristin and linezolid, the need for new, effective agents to treat multi-drug-resistant Gram-positive infections remains important. This review focuses on agents presently in clinical development for the treatment of serious multidrug-resistant staphylococcal, enterococcal and pneumococcal infections, including methicillin-resistant Staphylococcus aureus, vancomycin-resistant enterococci and penicillin-resistant Streptococcus pneumoniae. Agents to be discussed that affect the prokaryotic cell wall include the antimethicillin-resistant S. aureus cephalosporins BAL9141 and RWJ-54428, the glycopeptides oritavancin and dalbavancin and the lipopeptide daptomycin. Topoisomerase inhibitors include the fluoroquinolones gemifloxacin, sitafloxacin and garenoxacin. Protein synthesis inhibitors are represented by the ketolides telithromycin and cethromycin, the oxazolidinones and the glycylcycline tigecycline. Although each of these compounds has demonstrated antibacterial activity against antibiotic-resistant pathogens, their final regulatory approval will depend on an acceptable clinical safety profile.

摘要

随着细菌临床耐药性的持续发展以及对最近上市的药物奎奴普丁-达福普汀和利奈唑胺产生耐药性,开发新型有效药物来治疗多重耐药革兰氏阳性菌感染的需求仍然十分重要。本综述聚焦于目前正在临床研发中用于治疗严重多重耐药葡萄球菌、肠球菌和肺炎球菌感染的药物,包括耐甲氧西林金黄色葡萄球菌、耐万古霉素肠球菌和耐青霉素肺炎链球菌。将讨论的影响原核细胞壁的药物包括抗耐甲氧西林金黄色葡萄球菌头孢菌素BAL9141和RWJ-54428、糖肽类药物奥利万星和达巴万星以及脂肽类药物达托霉素。拓扑异构酶抑制剂包括氟喹诺酮类药物吉米沙星、西他沙星和加雷沙星。蛋白质合成抑制剂以酮内酯类药物泰利霉素和塞红霉素、恶唑烷酮类药物以及甘氨酰环素类药物替加环素为代表。尽管这些化合物均已显示出对耐药病原体的抗菌活性,但其最终获得监管批准将取决于可接受的临床安全性。

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