Chapman Joanna, Abbott Elizabeth, Alber Dagmar G, Baxter Robert C, Bithell Sian K, Henderson Elisa A, Carter Malcolm C, Chambers Phil, Chubb Ann, Cockerill G Stuart, Collins Peter L, Dowdell Verity C L, Keegan Sally J, Kelsey Richard D, Lockyer Michael J, Luongo Cindy, Najarro Pilar, Pickles Raymond J, Simmonds Mark, Taylor Debbie, Tyms Stan, Wilson Lara J, Powell Kenneth L
Arrow Therapeutics Ltd., Britannia House, 7 Trinity Street, London SE1 1DB, United Kingdom.
Antimicrob Agents Chemother. 2007 Sep;51(9):3346-53. doi: 10.1128/AAC.00211-07. Epub 2007 Jun 18.
Respiratory syncytial virus (RSV) is the most common cause of lower respiratory tract infections worldwide, yet no effective vaccine or antiviral treatment is available. Here we report the discovery and initial development of RSV604, a novel benzodiazepine with submicromolar anti-RSV activity. It proved to be equipotent against all clinical isolates tested of both the A and B subtypes of the virus. The compound has a low rate of in vitro resistance development. Sequencing revealed that the resistant virus had mutations within the nucleocapsid protein. This is a novel mechanism of action for anti-RSV compounds. In a three-dimensional human airway epithelial cell model, RSV604 was able to pass from the basolateral side of the epithelium effectively to inhibit virus replication after mucosal inoculation. RSV604, which is currently in phase II clinical trials, represents the first in a new class of RSV inhibitors and may have significant potential for the effective treatment of RSV disease.
呼吸道合胞病毒(RSV)是全球下呼吸道感染最常见的病因,但目前尚无有效的疫苗或抗病毒治疗方法。在此,我们报告了RSV604的发现及初步研发情况,RSV604是一种新型苯二氮䓬类药物,具有亚微摩尔级别的抗RSV活性。事实证明,它对该病毒A和B亚型的所有测试临床分离株均具有同等效力。该化合物体外耐药性产生率较低。测序显示,耐药病毒的核衣壳蛋白发生了突变。这是抗RSV化合物一种新的作用机制。在三维人气道上皮细胞模型中,RSV604能够从上皮细胞的基底外侧有效转运,在黏膜接种后抑制病毒复制。目前处于II期临床试验阶段的RSV604代表了一类新型RSV抑制剂中的首个药物,可能对有效治疗RSV疾病具有巨大潜力。