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用表达日本脑炎病毒(JEV)prM和E基因的高度减毒痘苗病毒MVA株免疫小鼠,可保护其免受致死性日本脑炎病毒感染。

Protection against lethal Japanese encephalitis virus infection of mice by immunization with the highly attenuated MVA strain of vaccinia virus expressing JEV prM and E genes.

作者信息

Nam J H, Wyatt L S, Chae S L, Cho H W, Park Y K, Moss B

机构信息

Department of Viral Disease, Korean NIH, Seoul, Korea.

出版信息

Vaccine. 1999 Jan 21;17(3):261-8. doi: 10.1016/s0264-410x(98)00156-x.

Abstract

Genes encoding the glycosylated precursor of the membrane (prM) and envelope (E) proteins of a Korean strain of Japanese encephalitis virus (JEV) were inserted into the genome of the host-range restricted, highly attenuated, and safety-tested MVA strain of vaccinia virus. MVA recombinants containing the JEV genes, under strong synthetic or modified H5 vaccinia virus promoters, were isolated. Synthesis of JEV prM and E proteins was detected by immunofluorescence microscopy, flow cytometry, and polyacrylamide gel electrophoresis. Mice inoculated and boosted by various routes with either of the MVA recombinants produced JEV neutralizing antibodies, that had titres comparable with those induced by an inactivated JEV vaccine, as well as haemagglutination-inhibiting antibodies. Mice immunized with 2 x 10(6) infectious units of MVA/JEV recombinants by intramuscular or intraperitoneal routes were completely protected against a 10(5) LD50 JEV challenge at 9 weeks of age.

摘要

将编码一株韩国乙型脑炎病毒(JEV)膜(prM)和包膜(E)蛋白糖基化前体的基因插入宿主范围受限、高度减毒且经过安全性测试的痘苗病毒MVA株的基因组中。在强合成或修饰的H5痘苗病毒启动子控制下,分离出含有JEV基因的MVA重组体。通过免疫荧光显微镜、流式细胞术和聚丙烯酰胺凝胶电泳检测JEV prM和E蛋白的合成。用任一MVA重组体通过各种途径接种和加强免疫的小鼠产生了JEV中和抗体,其滴度与灭活JEV疫苗诱导的滴度相当,同时还产生了血凝抑制抗体。通过肌肉内或腹腔内途径用2×10⁶感染单位的MVA/JEV重组体免疫的小鼠在9周龄时完全抵抗了10⁵ LD50 JEV的攻击。

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