表达单纯疱疹病毒基因的活痘苗病毒重组体。

J F Rooney, C R Wohlenberg, B Moss, A L Notkins
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引用次数: 12

摘要

表达单纯疱疹病毒(HSV)抗原的重组痘苗病毒已被测试作为预防单纯疱疹病毒感染的潜在活病毒疫苗。我们描述了三种牛痘病毒/HSV重组。第一个表达HSV-1糖蛋白D(痘苗/gD),第二个表达HSV-1糖蛋白B(痘苗/gB),第三个同时表达HSV-1糖蛋白D和流感A血凝素(痘苗/ hsv - gD/流感)。用牛痘/gD或牛痘/gB免疫的小鼠在体外产生了能够中和HSV的抗体,并对HSV的致死性和潜伏性感染都有保护作用。牛痘/gD免疫小鼠对HSV攻击的保护持续超过1年。牛痘/gD免疫小鼠对HSV的免疫应答可通过牛痘/gD加强接种而增强。然而,在牛痘/gD疫苗接种前,用表达非HSV基因的痘苗重组疫苗免疫的动物对HSV的免疫反应降低。在单独的实验中,构建了一种双价重组痘苗/HSVgD/流感病毒,并发现在免疫原性和对致命HSV攻击的保护作用方面与痘苗/gD单价重组痘苗/流感病毒相当。我们得出结论,痘苗/HSV重组体可以对小鼠的HSV感染提供保护,并且这些重组体可能为开发针对HSV的活病毒疫苗提供一种替代方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Live vaccinia virus recombinants expressing herpes simplex virus genes.

Vaccinia virus recombinants expressing antigens from herpes simplex virus (HSV) have been tested as potential live virus vaccines for prevention of HSV infection. We describe three vaccinia virus/HSV recombinants. The first expresses the HSV-1 glycoprotein D (vaccinia/gD), the second expresses the HSV-1 glycoprotein B (vaccinia/gB), and the third expresses both the HSV-1 glycoprotein D and the influenza A hemagglutinin (vaccinia/HSVgD/influenza). Mice immunized with vaccinia/gD or vaccinia/gB developed antibodies capable of neutralizing HSV in vitro and were protected against both lethal and latent infection with HSV. Protection against HSV challenge persisted for greater than 1 year in mice immunized with vaccinia/gD. The immune response to HSV in mice immunized with vaccinia/gD could be increased by a booster vaccination with vaccinia/gD. However, the immune response to HSV was decreased in animals immunized with a vaccinia recombinant that expressed non-HSV genes before vaccination with vaccinia/gD. In separate experiments, a bivalent vaccinia recombinant, vaccinia/HSVgD/influenza, was constructed and was found to be comparable to the vaccinia/gD single recombinant in immunogenicity and protective efficacy against lethal HSV challenge. We conclude that vaccinia/HSV recombinants can provide protection against HSV infection in mice and that these recombinants may provide an alternative approach in the development of a live virus vaccine against HSV.

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