联合核衣壳疫苗诱导强烈的SARS-CD8+ t细胞免疫反应。

Ali Azizi, Susan Aucoin, Helina Tadesse, Rita Frost, Masoud Ghorbani, Catalina Soare, Turaya Naas, Francisco Diaz-Mitoma
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引用次数: 3

摘要

一些研究表明,细胞介导的免疫反应在控制病毒复制中起着至关重要的作用。因此,候选SARS疫苗应引起广泛的CD8+ t细胞免疫反应。几组小鼠分别单独或联合sars -核衣壳免疫原免疫。在接受编码sars核衣壳、蛋白和XIAP的DNA作为佐剂的小鼠中,证实了高水平的特异性SARS-CD8+ t细胞应答。我们还观察到,在免疫小鼠中,同时给药表达核衣壳、重组蛋白和montanide/CpG的质粒可诱导高抗体滴度。此外,这种疫苗方法作为一种潜在的SARS候选疫苗值得进一步研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

A combined nucleocapsid vaccine induces vigorous SARS-CD8+ T-cell immune responses.

A combined nucleocapsid vaccine induces vigorous SARS-CD8+ T-cell immune responses.

A combined nucleocapsid vaccine induces vigorous SARS-CD8+ T-cell immune responses.

A combined nucleocapsid vaccine induces vigorous SARS-CD8+ T-cell immune responses.

Several studies have shown that cell-mediated immune responses play a crucial role in controlling viral replication. As such, a candidate SARS vaccine should elicit broad CD8+ T-cell immune responses. Several groups of mice were immunized alone or in combination with SARS-nucleocapsid immunogen. A high level of specific SARS-CD8+ T-cell response was demonstrated in mice that received DNA encoding the SARS-nucleocapsid, protein and XIAP as an adjuvant. We also observed that co-administration of a plasmid expressing nucleocapsid, recombinant protein and montanide/CpG induces high antibody titers in immunized mice. Moreover, this vaccine approach merits further investigation as a potential candidate vaccine against SARS.

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