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首页> 外文期刊>Vaccine >Expression of the B-cell and T-cell epitopes of the rabies virus nucleoprotein in Mycobacterium bovis BCG and induction of an humoral response in mice
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Expression of the B-cell and T-cell epitopes of the rabies virus nucleoprotein in Mycobacterium bovis BCG and induction of an humoral response in mice

机译:狂犬病病毒核蛋白中B细胞和T细胞表位在牛分枝杆菌BCG中的表达及体液反应的诱导

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摘要

Expression vectors containing rabies virus nucleoprotein B-cell and T-cell epitopes in Mycobacterium bovis BCG were constructed. The epitopes were subcloned into the M. leprae 18-kDa gene to ensure correct presentation to the host immune system. Expression of the 18-kDa::B+T epitope fusion protein was driven by either the hsp60 promoter, which is constitutively activated at a high level in M. bovis BCG, or the 18-kDa promoter, which is strongly induced in vivo. Mice were immunised intra-peritoneally with the recombinant BCG cultures and compared to a control group vaccinated with the commercial rabies vaccine Rai-SAD. Both of the expression vectors elicited a higher antibody titre than that of the rabies vaccine, with the highest response shown by M. bovis BCG (pUP203), expression controlled by the 18-kDa promoter. Immunisation. with M bovis BCG (pUP202), expression controlled by the hsp60 promoter, resulted in a continuously increasing antibody titre up to 60 days post immunisation. The mice antibodies were also capable of recognising the whole rabies virus and not only the synthetic peptide epitopes.
机译:构建了牛分枝杆菌BCG中含有狂犬病毒核蛋白B细胞和T细胞表位的表达载体。将表位亚克隆到麻风杆菌18-kDa基因中,以确保正确呈现给宿主免疫系统。 18-kDa :: B + T表位融合蛋白的表达受hsp60启动子(在牛分枝杆菌BCG中被高水平组成性激活)或18-kDa启动子(在体内强烈诱导)驱动。用重组BCG培养物腹膜内免疫小鼠,并与接种商业狂犬病疫苗Rai-SAD的对照组进行比较。两种表达载体均比狂犬病疫苗引起更高的抗体效价,牛分枝杆菌BCG(pUP203)显示出最高的应答,表达受18-kDa启动子控制。免疫。由hsp60启动子控制的M bovis BCG(pUP202)的表达导致抗体滴度持续提高,直至免疫后60天。小鼠抗体还能够识别整个狂犬病毒,而不仅仅是合成的肽表位。

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