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一种对脊髓灰质炎病毒易感的转基因小鼠模型,可作为口服脊髓灰质炎疫苗猴神经毒力试验的可能替代方法。

A poliovirus-susceptible transgenic mouse model as a possible replacement for the monkey neurovirulence test of oral poliovirus vaccine.

作者信息

Dragunsky E, Taffs R, Chernokhvostova Y, Nomura T, Hioki K, Gardner D, Norwood L, Levenbook I

机构信息

Center for Biologics Evaluation and Research, Food and Drug Administration, Bethesda, Maryland 20892, USA.

出版信息

Biologicals. 1996 Jun;24(2):77-86. doi: 10.1006/biol.1996.0010.

Abstract

Two poliovirus-susceptible transgenic mouse (Tg PVR) strains, Tg1 and Tg21, were compared with the monkey test for their sensitivity to neurovirulence of live oral poliovirus vaccine (OPV). Intracerebral (i.c.) and intraspinal (i.s.) routes of inoculation were investigated to determine the most suitable combination of mouse strain and route. Evaluation of the mouse tests was performed using several indicators; clinical score and failure time were selected as the most efficient. Tg1 and Tg21 mice inoculated i.s. with type 2, and Tg21 mice inoculated i.s. with type 3 OPV were determined to be the most appropriate systems, whereas they are shown not to be suitable for type 1 OPV. The sensitivity of each of the two mouse models was at least equal to that of the monkey test, suggesting that these mouse systems might be considered as a potential replacement for the monkey test of OPV. However, more data are needed to establish regulatory criteria of acceptability for vaccine lots tested in Tg PVR mice. This is the first study conducted with Tg PVR mice with all three types of poliovirus vaccine preparations.

摘要

将两种对脊髓灰质炎病毒敏感的转基因小鼠(Tg PVR)品系Tg1和Tg21,与猴试验进行比较,以评估它们对口服脊髓灰质炎减毒活疫苗(OPV)神经毒力的敏感性。研究了脑内(i.c.)和脊髓内(i.s.)接种途径,以确定小鼠品系和接种途径的最合适组合。使用多个指标对小鼠试验进行评估;临床评分和发病时间被选为最有效的指标。确定经脊髓内接种2型OPV的Tg1和Tg21小鼠,以及经脊髓内接种3型OPV的Tg21小鼠是最合适的系统,然而,它们不适用于1型OPV。两种小鼠模型中每一种的敏感性至少与猴试验相当,这表明这些小鼠系统可被视为OPV猴试验的潜在替代方法。然而,需要更多数据来确立在Tg PVR小鼠中检测疫苗批次的可接受性监管标准。这是首次使用Tg PVR小鼠对所有三种脊髓灰质炎病毒疫苗制剂进行的研究。

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