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基于病毒颗粒结构和分子研究的新一代非洲马瘟病毒疫苗。

New generation of African horse sickness virus vaccines based on structural and molecular studies of the virus particles.

作者信息

Roy P, Sutton G

机构信息

Department of Biochemistry, University of Oxford, U.K.

出版信息

Arch Virol Suppl. 1998;14:177-202. doi: 10.1007/978-3-7091-6823-3_17.

Abstract

African horse sickness virus (AHSV) is a member of the genus Orbivirus, which also includes bluetongue virus (BTV) and epizootic haemorrhagic disease (EHDV) virus. These orbiviruses have similar morphological and biochemical properties, with distinctive pathobiological properties and host ranges. Sequencing studies of the capsid proteins have revealed evolutionary relationships between these viruses. Biochemical studies of the viruses together with the expression of individual proteins and protein complexes have resulted in the development of new generation vaccines. Baculovirus expressed AHSV VP2 provides protection against death caused by AHSV challenge. Similarly, BTV VP2 alone elicits protective neutralising antibodies against BTV in sheep, which is enhanced in the presence of VP5. Recent developments in biotechnology (multiple gene expression baculovirus systems) have made it possible to synthesise orbivirus particles that biochemically and immunologically mimic authentic virions but lack the genetic material. Particle doses as low as 10 micrograms elicit responses that are sufficient to protect sheep 15 months post vaccination, against virulent virus challenge. Moreover, knowledge of the three dimensional structure of these particles enables us to engineer them to deliver multiple foreign peptide components representing other viral epitopes (e.g. foot and mouth disease virus and influenza virus) in order to elicit protective immunity.

摘要

非洲马瘟病毒(AHSV)是环状病毒属的成员,该属还包括蓝舌病病毒(BTV)和流行性出血病病毒(EHDV)。这些环状病毒具有相似的形态和生化特性,但具有独特的病理生物学特性和宿主范围。对衣壳蛋白的测序研究揭示了这些病毒之间的进化关系。对这些病毒的生化研究以及单个蛋白质和蛋白质复合物的表达促成了新一代疫苗的研发。杆状病毒表达的AHSV VP2可提供针对AHSV攻击所致死亡的保护作用。同样,单独的BTV VP2可在绵羊体内引发针对BTV的保护性中和抗体,在VP5存在时这种抗体水平会增强。生物技术的最新进展(多基因表达杆状病毒系统)使得合成在生化和免疫方面模拟真实病毒体但缺乏遗传物质的环状病毒颗粒成为可能。低至10微克的颗粒剂量所引发的反应足以在接种疫苗15个月后保护绵羊免受强毒病毒攻击。此外,对这些颗粒三维结构的了解使我们能够对其进行改造,以递送代表其他病毒表位(如口蹄疫病毒和流感病毒)的多种外源肽成分,从而引发保护性免疫。

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