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灭活脊髓灰质炎病毒疫苗可保护转基因脊髓灰质炎病毒受体小鼠免受3型脊髓灰质炎病毒攻击。

Inactivated poliovirus vaccine protects transgenic poliovirus receptor mice against type 3 poliovirus challenge.

作者信息

Taffs R E, Chernokhvostova Y V, Dragunsky E M, Nomura T, Hioki K, Beuvery E C, Fitzgerald E A, Levenbook I S, Asher D M

机构信息

Food and Drug Administration, Rockville, Maryland, USA.

出版信息

J Infect Dis. 1997 Feb;175(2):441-4. doi: 10.1093/infdis/175.2.441.

Abstract

Transgenic (Tg) mice expressing the human poliovirus receptor (PVR) were vaccinated with inactivated poliovirus vaccine (IPV) and evaluated for induced immunity against type 3 poliomyelitis. One injection of monovalent type 3 IPV elicited protective immunity against wild-type poliovirus. In contrast, 2 injections of trivalent IPV were required for protection. Neutralizing antibody response and protection were vaccine dose-dependent. Administration of polio-immune mouse plasma protected unimmunized mice, demonstrating that neutralizing antibody was sufficient for immunity. IPV heated to remove its D antigen component did not induce protection in Tg PVR mice. IPV derived from a wild-type poliovirus strain gave better protection against wild-type viral challenge than IPV derived from an attenuated poliovirus strain. The newly developed Tg PVR mouse-protection test may be useful in evaluating existing IPV potency tests and for attempts to improve formulations of trivalent IPV or combined vaccines for childhood immunization schedules.

摘要

用表达人脊髓灰质炎病毒受体(PVR)的转基因(Tg)小鼠接种灭活脊髓灰质炎疫苗(IPV),并评估其针对3型脊髓灰质炎诱导的免疫力。单次注射单价3型IPV可引发针对野生型脊髓灰质炎病毒的保护性免疫。相比之下,需要注射2次三价IPV才能提供保护。中和抗体反应和保护作用呈疫苗剂量依赖性。给予脊髓灰质炎免疫小鼠的血浆可保护未免疫的小鼠,这表明中和抗体足以提供免疫保护。加热去除其D抗原成分的IPV在Tg PVR小鼠中未诱导出保护作用。源自野生型脊髓灰质炎病毒株的IPV比源自减毒脊髓灰质炎病毒株的IPV对野生型病毒攻击提供更好的保护。新开发的Tg PVR小鼠保护试验可能有助于评估现有的IPV效力试验,并有助于尝试改进三价IPV或用于儿童免疫程序的联合疫苗的配方。

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