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A DNA vaccine induces SARS coronavirus neutralization and protective immunity in mice

机译:脱氧核糖核酸疫苗诱导SARS冠状病毒中和和小鼠保护性免疫

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Public health measures have successfully identified and contained outbreaks of the severe acute respiratory syndrome (SARS) coronavirus (SARS-CoV), but concerns remain over the possibility of future recurrences. Finding a vaccine for this virus therefore remains a high priority. Here, we show that a DNA vaccine encoding the spike (S) glycoprotein of the SARS-CoV induces T cell and neutralizing antibody responses, as well as protective immunity, in a mouse model. Alternative forms of S were analysed by DNA immunization. These expression vectors induced robust immune responses mediated by CD4 and CD8 cells, as well as significant antibody titres, measured by enzyme-linked immunosorbent assay. Moreover, antibody responses in mice vaccinated with an expression vector encoding a form of S that includes its transmembrane domain elicited neutralizing antibodies. Viral replication was reduced by more than six orders of magnitude in the lungs of mice vaccinated with these S plasmid DNA expression vectors, and protection was mediated by a humoral but not a T-cell-dependent immune mechanism. Gene-based vaccination for the SARS-CoV elicits effective immune responses that generate protective immunity in an animal model.
机译:公共卫生措施已成功识别并遏制了严重急性呼吸系统综合症(SARS)冠状病毒(SARS-CoV)的暴发,但对未来复发的可能性仍然存在担忧。因此,寻找这种病毒的疫苗仍然是高度优先事项。在这里,我们显示了编码SARS-CoV的尖峰(S)糖蛋白的DNA疫苗在小鼠模型中诱导T细胞和中和抗体反应以及保护性免疫。通过DNA免疫分析S的替代形式。这些表达载体诱导了由CD4和CD8细胞介导的强大免疫反应,以及通过酶联免疫吸附测定法测量的显着抗体滴度。此外,用编码S形式的表达载体(包括其跨膜结构域)接种的小鼠中的抗体应答引发中和抗体。用这些S质粒DNA表​​达载体接种的小鼠肺部病毒复制减少了六个数量级以上,并且保护作用是通过体液而非T细胞依赖性免疫机制介导的。 SARS-CoV的基于基因的疫苗接种可引发有效的免疫反应,从而在动物模型中产生保护性免疫。

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