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适用于人类的第一代爱泼斯坦-巴尔病毒疫苗制剂的验证。

Validation of a first-generation Epstein-Barr virus vaccine preparation suitable for human use.

作者信息

Morgan A J, Allison A C, Finerty S, Scullion F T, Byars N E, Epstein M A

机构信息

Department of Pathology, University of Bristol Medical School, University Walk, England.

出版信息

J Med Virol. 1989 Sep;29(1):74-8. doi: 10.1002/jmv.1890290114.

DOI:10.1002/jmv.1890290114
PMID:2555448
Abstract

The efficacy of a new vaccine preparation against Epstein-Barr (EB) virus was investigated in cotton-top tamarins. The vaccine consists of fast protein liquid chromatography-purified EB virus membrane antigen glycoprotein of 340 Kd (MA gp340) mixed with a synthetic muramyl dipeptide adjuvant emulsified in squalane containing a pluronic polymer; it is suitable for both scaled-up batch production and eventual administration to man. Vaccinated tamarins rapidly developed ELISA detectable high titre antibodies to MA gp340, and their sera became strongly EB virus-neutralising. After challenge with a massive 100% carcinogenic dose of EB virus, the vaccinated tamarins had a strikingly low level of circulating EB virus-carrying mononuclear cells, in contrast to a control animal, and remained entirely free of tumours. This first-generation vaccine has thus been validated in experimental animals and the way opened for a phase I human trial.

摘要

在棉顶狨猴中研究了一种针对爱泼斯坦 - 巴尔(EB)病毒的新型疫苗制剂的疗效。该疫苗由快速蛋白质液相色谱纯化的340Kd EB病毒膜抗原糖蛋白(MA gp340)与合成的胞壁酰二肽佐剂混合而成,该佐剂乳化在含有普朗尼克聚合物的角鲨烷中;它既适合大规模批量生产,最终也适合给人类使用。接种疫苗的狨猴迅速产生了ELISA可检测到的针对MA gp340的高滴度抗体,并且它们的血清具有很强的EB病毒中和能力。在用100%致癌剂量的EB病毒进行攻击后,与对照动物相比,接种疫苗的狨猴循环携带EB病毒的单核细胞水平极低,并且完全没有肿瘤。因此,这种第一代疫苗已在实验动物中得到验证,并为I期人体试验开辟了道路。

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J Med Virol. 1989 Sep;29(1):74-8. doi: 10.1002/jmv.1890290114.
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