• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

豚鼠模型中的沙粒病毒感染:用重组α干扰素、免疫调节剂CL246,738和利巴韦林进行抗病毒治疗。

Arenavirus infection in the guinea pig model: antiviral therapy with recombinant interferon-alpha, the immunomodulator CL246,738 and ribavirin.

作者信息

Lucia H L, Coppenhaver D H, Baron S

机构信息

Department of Pathology, Microbiology and Pediatrics, University of Texas Medical Branch, Galveston 77550.

出版信息

Antiviral Res. 1989 Dec;12(5-6):279-92. doi: 10.1016/0166-3542(89)90055-7.

DOI:10.1016/0166-3542(89)90055-7
PMID:2561334
Abstract

Human arenaviral infections have a high mortality, and are dangerous to work with in the laboratory. There is a need for good antiviral agents to treat these infections. Pichinde virus infection of the inbred strain 13 guinea pig is a relatively safe, good animal model for human arenavirus infections. Mortality is consistently 100% between days 12 and 25 (mean 14.8) days after infection. When infected animals were treated with recombinant human interferon alpha A, or with CL246,783, an immunomodulator known to induce interferon, no beneficial effect was noted. When animals received ribavirin, 25 mg/kg/day for the first 14 days of infection, the course of infection was prolonged, with death occurring a mean of 22.5 days after infection. If ribavirin was administered for 28 days, mortality was reduced to 25%, with those animals dying a mean of 21.0 days after infection. These results confirm the studies that indicate that ribavirin is a useful agent for treating arenaviral infections. However, treatment with this agent must be prolonged. They also demonstrate the potential usefulness of Pichinde virus infection in strain 13 guinea pigs as an animal model of human disease.

摘要

人类沙粒病毒感染死亡率很高,在实验室中处理这类病毒很危险。因此需要优良的抗病毒药物来治疗这些感染。近交系13豚鼠感染皮钦德病毒是一种相对安全的、用于人类沙粒病毒感染的良好动物模型。感染后第12至25天(平均14.8天)死亡率始终为100%。用重组人αA干扰素或CL246,783(一种已知可诱导干扰素的免疫调节剂)治疗感染动物,未观察到有益效果。感染动物在感染的前14天接受25mg/kg/天的利巴韦林治疗时,感染病程延长,平均在感染后22.5天死亡。如果利巴韦林给药28天,死亡率降至25%,这些动物平均在感染后21.0天死亡。这些结果证实了表明利巴韦林是治疗沙粒病毒感染有用药物的研究。然而,使用该药物治疗必须延长疗程。它们还证明了13系豚鼠感染皮钦德病毒作为人类疾病动物模型的潜在用途。

相似文献

1
Arenavirus infection in the guinea pig model: antiviral therapy with recombinant interferon-alpha, the immunomodulator CL246,738 and ribavirin.豚鼠模型中的沙粒病毒感染:用重组α干扰素、免疫调节剂CL246,738和利巴韦林进行抗病毒治疗。
Antiviral Res. 1989 Dec;12(5-6):279-92. doi: 10.1016/0166-3542(89)90055-7.
2
Combinatorial ribavirin and interferon alfacon-1 therapy of acute arenaviral disease in hamsters.利巴韦林与干扰素α-1联合治疗仓鼠急性沙粒病毒病
Antivir Chem Chemother. 2006;17(4):175-83. doi: 10.1177/095632020601700402.
3
Effect of ribavirin on junin virus infection in guinea pigs.利巴韦林对感染瓜那利托病毒豚鼠的影响。
Zoonoses Public Health. 2012 Jun;59(4):278-85. doi: 10.1111/j.1863-2378.2011.01447.x. Epub 2012 Jan 2.
4
Treatment of late stage disease in a model of arenaviral hemorrhagic fever: T-705 efficacy and reduced toxicity suggests an alternative to ribavirin.在沙粒病毒出血热模型中对晚期疾病的治疗:T-705的疗效及毒性降低表明其可作为利巴韦林的替代药物。
PLoS One. 2008;3(11):e3725. doi: 10.1371/journal.pone.0003725. Epub 2008 Nov 14.
5
Interferon alfacon-1 protects hamsters from lethal pichinde virus infection.干扰素α-1可保护仓鼠免受致死性皮钦德病毒感染。
Antimicrob Agents Chemother. 2005 Jun;49(6):2378-86. doi: 10.1128/AAC.49.6.2378-2386.2005.
6
In vitro and in vivo activities of T-705 against arenavirus and bunyavirus infections.T-705 对沙粒病毒和布尼亚病毒感染的体外及体内活性
Antimicrob Agents Chemother. 2007 Sep;51(9):3168-76. doi: 10.1128/AAC.00356-07. Epub 2007 Jul 2.
7
Effect of ribavirin and tributylribavirin on argentine hemorrhagic fever (Junin virus) in guinea pigs.利巴韦林和三丁基利巴韦林对豚鼠阿根廷出血热(胡宁病毒)的影响。
Antimicrob Agents Chemother. 1986 Mar;29(3):521-3. doi: 10.1128/AAC.29.3.521.
8
Treatment of lethal Pichinde virus infections in weanling LVG/Lak hamsters with ribavirin, ribamidine, selenazofurin, and ampligen.用利巴韦林、硝唑咪、硒唑嘌呤和安普利近治疗断奶期LVG/Lak仓鼠的致死性皮钦德病毒感染。
Antiviral Res. 1993 Jan;20(1):57-70. doi: 10.1016/0166-3542(93)90059-r.
9
Varying role of alpha/beta interferon in the antiviral efficacy of synthetic immunomodulators against Semliki Forest virus infection.α/β干扰素在合成免疫调节剂抗塞姆利基森林病毒感染的抗病毒疗效中的不同作用。
Antiviral Res. 1991 Mar-Apr;15(3):241-54. doi: 10.1016/0166-3542(91)90070-8.
10
Characterization of murine Caraparu Bunyavirus liver infection and immunomodulator-mediated antiviral protection.小鼠卡拉帕鲁布尼亚病毒肝脏感染及免疫调节剂介导的抗病毒保护作用的特征分析
Antiviral Res. 1993 Feb;20(2):155-71. doi: 10.1016/0166-3542(93)90005-4.

引用本文的文献

1
Development of real-time reverse transcriptase qPCR assays for the detection of Punta Toro virus and Pichinde virus.用于检测蓬塔托罗病毒和皮钦德病毒的实时逆转录定量聚合酶链反应检测方法的开发。
Virol J. 2016 Mar 31;13:54. doi: 10.1186/s12985-016-0509-3.
2
Viral quasispecies evolution.病毒准种进化。
Microbiol Mol Biol Rev. 2012 Jun;76(2):159-216. doi: 10.1128/MMBR.05023-11.
3
Junín virus infection activates the type I interferon pathway in a RIG-I-dependent manner.胡宁病毒感染通过 RIG-I 依赖性方式激活 I 型干扰素通路。
PLoS Negl Trop Dis. 2012;6(5):e1659. doi: 10.1371/journal.pntd.0001659. Epub 2012 May 22.
4
Effective oral favipiravir (T-705) therapy initiated after the onset of clinical disease in a model of arenavirus hemorrhagic Fever.在沙粒病毒出血热模型中,于临床疾病发作后开始有效的口服法匹拉韦(T-705)治疗。
PLoS Negl Trop Dis. 2011 Oct;5(10):e1342. doi: 10.1371/journal.pntd.0001342. Epub 2011 Oct 11.
5
Ribavirin can be mutagenic for arenaviruses.利巴韦林可能使沙粒病毒产生突变。
J Virol. 2011 Jul;85(14):7246-55. doi: 10.1128/JVI.00614-11. Epub 2011 May 11.
6
Evaluation of Lassa antiviral compound ST-193 in a guinea pig model.评价拉沙抗病毒化合物 ST-193 在豚鼠模型中的作用。
Antiviral Res. 2011 Apr;90(1):70-9. doi: 10.1016/j.antiviral.2011.02.012. Epub 2011 Mar 1.
7
Interferon alfacon-1 protects hamsters from lethal pichinde virus infection.干扰素α-1可保护仓鼠免受致死性皮钦德病毒感染。
Antimicrob Agents Chemother. 2005 Jun;49(6):2378-86. doi: 10.1128/AAC.49.6.2378-2386.2005.