Morrey John D, Day Craig W, Julander Justin G, Blatt Lawrence M, Smee Donald F, Sidwell Robert W
Institute for Antiviral Research, Department of Animal, Dairy & Veterinary Sciences, Utah State University, Logan, UT, USA.
Antivir Chem Chemother. 2004 Mar;15(2):101-9. doi: 10.1177/095632020401500202.
The recent West Nile virus (WNV) outbreak in the United States has increased the need to identify effective therapies. Studies were conducted in cell culture and in rodent animal models to determine the efficacy of interferon-alpha (IFN-alpha), interferon (IFN) inducers and ribavirin, alone or in combination with IFN, in treating WNV. Intraperitoneal injection of IFN-alpha B/D (qd for 7 days), polyI-polyC(12)U [Ampligen (every other day for 7 days)] and topically applied imiquimod (qd for 7 days), administered from 1 day before viral challenge, were effective in protecting, respectively, 100%, 100% and 70% of BALB/c mice from mortality induced by subcutaneous injection of WNV. When IFN-alpha B/D or Ampligen treatments were delayed to 4-6 h before viral challenge in mice, efficacy was greatly diminished. Infected Syrian golden hamsters treated with interferon alphacon-1 (Infergen) and Ampligen 4-6 h before viral challenge gained more weight and had a greater survival than saline-treated animals. A combination study of subcutaneously administered Infergen (5 to 0.05 microg/kg/day) and ribavirin (75 to 7.5 mg/kg/day) in >7 week old hamsters demonstrated that Infergen was slightly efficacious in reducing mortality and disease signs; however, it was not synergistic in its antiviral effects when combined with ribavirin. Ribavirin treatment alone increased mortality of infected hamsters. The reduced mortality correlated with reduced plasma viraemia. Since WNV-infected patients have already been treated with IFN and ribavirin and future clinical trials have been suggested, this first report of IFN alone or in combination with ribavirin in WNV-infected animal models might provide useful information for subsequent treatment of patients.
近期美国爆发的西尼罗河病毒(WNV)疫情增加了对有效治疗方法的需求。在细胞培养和啮齿动物模型中开展了研究,以确定α干扰素(IFN-α)、干扰素(IFN)诱导剂和利巴韦林单独使用或与IFN联合使用治疗WNV的疗效。从病毒攻击前1天开始,腹腔注射IFN-α B/D(每天1次,共7天)、聚肌胞苷酸(12)U [惠福仁(每隔1天1次,共7天)]以及局部应用咪喹莫特(每天1次,共7天),分别使100%、100%和70%的BALB/c小鼠免受皮下注射WNV所致的死亡。当在小鼠中把IFN-α B/D或惠福仁治疗推迟到病毒攻击前4 - 6小时时,疗效大大降低。在病毒攻击前4 - 6小时用干扰素α - con1(干复津)和惠福仁治疗的受感染叙利亚金黄地鼠比用生理盐水治疗的动物体重增加更多,存活时间更长。在7周龄以上的地鼠中皮下联合给予干复津(5至0.05微克/千克/天)和利巴韦林(75至7.5毫克/千克/天)的联合研究表明,干复津在降低死亡率和疾病体征方面有轻微疗效;然而,它与利巴韦林联合使用时在抗病毒作用上并无协同作用。单独使用利巴韦林治疗会增加受感染地鼠的死亡率。死亡率降低与血浆病毒血症降低相关。由于WNV感染患者已经接受过IFN和利巴韦林治疗,并且有人建议开展未来的临床试验,这份关于IFN单独或与利巴韦林联合用于WNV感染动物模型的首份报告可能会为后续患者治疗提供有用信息。