Infectious Diseases, Medicinal Research Laboratories, Shionogi & Co, Ltd, Toyonaka, Osaka, Japan.
Antimicrob Agents Chemother. 2013 May;57(5):2286-94. doi: 10.1128/AAC.02324-12. Epub 2013 Mar 11.
The efficacy of intravenous peramivir against influenza A (H1N1) 2009 virus infection was evaluated in mice in which the immune system was suppressed by cyclophosphamide (CP) treatment. The mortality rate of the vehicle control group was 100%, and the mice lost 20% of their body weight on average by day 13 postinfection (p.i.). Repeated administration of peramivir (40 mg/kg of body weight once a day, given intravenously for 20 days), starting at 1 h p.i., significantly reduced mortality, body weight loss, viral titers, and cytokine production in infected mice compared with results for administration of vehicle (P < 0.01). In addition, repeated administration of peramivir, starting at 24 h, 48 h, or 72 h p.i., also resulted in increases in survival rates and reduction of viral titers in the lungs (P < 0.01). The mean days to death (MDD) of the vehicle group was 14.5 days, while in the groups treated with peramivir starting at 24 h, 48 h, and 72 h p.i., the MDDs were >23.0, 20.9, and 21.8 days, respectively. In comparison, repeated administration of oseltamivir phosphate (5 mg/kg twice a day, given orally for 20 days), starting at 24 h, 48 h, and 72 h p.i., also significantly prevented body weight loss, whereas no significant differences in mortality rates and viral titers in the lungs were observed compared with results for the vehicle group. These data indicated that repeated administration of peramivir was effective in promoting the survival and reducing virus replication in immunosuppressed mice infected with influenza A (H1N1) 2009 virus.
在环磷酰胺(CP)处理抑制免疫系统的小鼠中评估了静脉用帕拉米韦对甲型 H1N1 2009 流感病毒感染的疗效。载体对照组的死亡率为 100%,感染后第 13 天,小鼠平均体重减轻 20%。从感染后 1 小时开始,每天重复静脉注射帕拉米韦(40mg/kg 体重,连续 20 天)可显著降低感染小鼠的死亡率、体重减轻、病毒滴度和细胞因子产生,与载体组相比差异有统计学意义(P<0.01)。此外,从感染后 24、48 或 72 小时开始重复给予帕拉米韦,也可提高存活率并降低肺部的病毒滴度(P<0.01)。载体组的平均死亡天数(MDD)为 14.5 天,而从感染后 24、48 和 72 小时开始给予帕拉米韦治疗的组的 MDD 分别为>23.0、20.9 和 21.8 天。相比之下,从感染后 24、48 和 72 小时开始重复给予磷酸奥司他韦(5mg/kg,每天两次,连续 20 天,口服)也可显著防止体重减轻,但与载体组相比,死亡率和肺部病毒滴度无显著差异。这些数据表明,重复给予帕拉米韦可有效促进免疫抑制感染甲型 H1N1 2009 流感病毒的小鼠的存活并降低病毒复制。