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[评估ERA狂犬病疫苗在不同免疫后时期对狂犬病病毒抗原变异株的效果]

[Evaluation of the ERA antirabies vaccine against antigenic variants of rabies virus in various post-immunization periods].

作者信息

Cordeiro C C, Silva E V, Miguel O, Germano P M

机构信息

Laboratório Regional de Apoio Animal (LARA), do Ministério da Agricultura, Campinas, SP, Brasil.

出版信息

Rev Saude Publica. 1990 Dec;24(6):512-7. doi: 10.1590/s0034-89101990000600010.

Abstract

Protection levels of an attenuated antirabies vaccine, of ERA origin, prepared in Kidney tissue culture, were evaluated in mice. Two schemes of vaccination were utilized: a single dose and 6 doses on alternate days. Animals of different experimental groups were challenged at 15, 30, 60 and 120 days postimmunization with six antigenic variants of rabies virus: strains of dog origin (S. Paulo, Brazil and Nigeria), vampire origin (DR-19 and Pernambuco, Brazil), fox origin (Rio Grande do Norte, Brazil), and CVS (Challenge Virus Standard). The results showed the effectiveness of the ERA vaccine against all antigenic variants of street and sylvatic rabies virus, independently of the vaccination scheme. Against the laboratory strains (DR-19 and CVS) the ERA vaccine was less effective, mainly in the groups vaccinated with a single dose.

摘要

对在肾组织培养物中制备的源自ERA的减毒抗狂犬病疫苗在小鼠中的保护水平进行了评估。采用了两种接种方案:单剂量和隔日接种6剂。不同实验组的动物在免疫后15、30、60和120天用狂犬病病毒的六种抗原变体进行攻击:犬源毒株(巴西圣保罗和尼日利亚)、吸血蝠源毒株(巴西DR - 19和伯南布哥)、狐源毒株(巴西北大河州)以及CVS(攻击病毒标准株)。结果表明,ERA疫苗对街毒株和野生动物狂犬病病毒的所有抗原变体均有效,与接种方案无关。对于实验室毒株(DR - 19和CVS),ERA疫苗效果较差,主要是在单剂量接种的组中。

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