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在小鼠脑内水疱性口炎病毒增殖开始后启动的外源性干扰素治疗的疗效。

Efficacy of exogenous interferon treatment initiated after onset of multiplication of vesicular stomatitis virus in the brains of mice.

作者信息

Gresser I, Tovey M G, Bourali-Maury C

出版信息

J Gen Virol. 1975 Jun;27(3):395-8. doi: 10.1099/0022-1317-27-3-395.

DOI:10.1099/0022-1317-27-3-395
PMID:167120
Abstract

Initiation of treatment with potent interferon preparations (6-4 x 10-6 units per dose) 4 days after intranasal inoculation of VSV (at a time when virus has already multiplied in the brains of most mice) resulted in a marked increase in mouse survival. In a series of 6 experiments only 11 to 18% of control mice survived whereas 52% of interferon treated mice survival. These results suggest the usefulness of exogenous interferon even when treatment is begun late in the course of an acute virus disease.

摘要

在用VSV经鼻接种4天后(此时病毒已在大多数小鼠的脑中增殖)开始用强效干扰素制剂进行治疗(每剂6 - 4×10⁻⁶单位),可使小鼠存活率显著提高。在一系列6个实验中,对照小鼠仅有11%至18%存活,而接受干扰素治疗的小鼠有52%存活。这些结果表明,即使在急性病毒病病程后期开始治疗,外源性干扰素也是有用的。

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Efficacy of exogenous interferon treatment initiated after onset of multiplication of vesicular stomatitis virus in the brains of mice.在小鼠脑内水疱性口炎病毒增殖开始后启动的外源性干扰素治疗的疗效。
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Mediators of protection against lethal systemic vesicular stomatitis virus infection in hamsters: defective interfering particles, polyinosinate-polycytidylate, and interferon.
仓鼠抵抗致死性系统性水疱性口炎病毒感染的保护介质:缺陷干扰颗粒、聚肌苷酸-聚胞苷酸和干扰素。
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4
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Infect Immun. 1980 Nov;30(2):513-22. doi: 10.1128/iai.30.2.513-522.1980.
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Animal models in interferon research: some current trends.干扰素研究中的动物模型:当前的一些趋势。
Experientia. 1989 Jun 15;45(6):558-62. doi: 10.1007/BF01990506.
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