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利巴韦林与干扰素α-1联合治疗仓鼠急性沙粒病毒病

Combinatorial ribavirin and interferon alfacon-1 therapy of acute arenaviral disease in hamsters.

作者信息

Gowen Brian B, Smee Donald F, Wong Min-Hui, Pace Anne M, Jung Kie-Hoon, Bailey Kevin W, Blatt Lawrence M, Sidwell Robert W

机构信息

Institute for Antiviral Research, Utah State University, Logan, UT, USA.

出版信息

Antivir Chem Chemother. 2006;17(4):175-83. doi: 10.1177/095632020601700402.

DOI:10.1177/095632020601700402
PMID:17066896
Abstract

Several arenaviruses endemic to South America (Junin, Machupo, and Guanarito) and Africa (Lassa) are known to cause frequently fatal haemorrhagic fever. With the exception of ribavirin, which has demonstrated efficacy in cases of Lassa fever, there is no other effective therapeutic for the treatment of arenaviral haemorrhagic fever. We have recently reported that consensus interferon-a (IFN alfacon-1) can protect hamsters from lethal Pichinde virus (PCV) infection, which serves as a model for acute arenaviral disease in humans. Here we demonstrate highly effective therapy through the combined use of ribavirin with IFN alfacon-1 for the treatment of PCV infection in hamsters. Ribavirin was given orally, twice per day for 7 days, and IFN alfacon-1 was administered intraperitoneally once per day for 10 days. Treatments were initiated 1-5 days post-virus challenge using various dose combinations, many of which were less than optimal when the drugs were given independently. Combining suboptimal doses of ribavirin (5-10 mg/kg/day) with IFN alfacon-1 (5-10 microg/kg/day), we were able to demonstrate increased protection from mortality, reduced viral burden and liver disease, and greatly extended survival times as compared to treatments where drugs were administered alone. Our data indicate that combination therapy results in synergistic activity that may slow down the progression of the disease and decrease fatality rates associated with severe arenaviral infections in humans. Further, combination therapy reduces the effective dosage of ribavirin, which would serve to limit its toxicity.

摘要

南美洲(胡宁病毒、马丘波病毒和瓜纳里托病毒)和非洲(拉沙病毒)特有的几种沙粒病毒已知会引发常常致命的出血热。除了在拉沙热病例中已证明有效的利巴韦林外,没有其他有效的疗法可用于治疗沙粒病毒出血热。我们最近报告称,共识干扰素-α(IFN alfacon-1)可保护仓鼠免受致死性皮钦德病毒(PCV)感染,PCV可作为人类急性沙粒病毒病的模型。在此,我们证明通过联合使用利巴韦林和IFN alfacon-1可对仓鼠的PCV感染进行高效治疗。利巴韦林口服给药,每天两次,共7天,IFN alfacon-1腹腔注射给药,每天一次,共10天。在病毒攻击后1 - 5天使用各种剂量组合开始治疗,其中许多剂量组合在单独使用药物时并非最佳剂量。将次优剂量的利巴韦林(5 - 10毫克/千克/天)与IFN alfacon-1(5 - 10微克/千克/天)联合使用,与单独给药治疗相比,我们能够证明可增强对死亡的保护、降低病毒载量和肝脏疾病,并大大延长存活时间。我们的数据表明,联合治疗产生协同活性,可能会减缓疾病进展并降低与人类严重沙粒病毒感染相关的死亡率。此外,联合治疗降低了利巴韦林的有效剂量,这将有助于限制其毒性。

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