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Single immunization with MF59-adjuvanted inactivated whole-virion H7N9 influenza vaccine provides early protection against H7N9 virus challenge in mice

机译:用MF59辅助灭活的全部病毒虫H7N9流感疫苗的单一免疫为小鼠的H7N9病毒攻击提供早期保护

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摘要

Abstract H7N9 influenza infection in humans would result in severe respiratory illness. Vaccination is the best way to prevent influenza virus. In this paper, we investigated the effect of early protection provided by inactivated whole-virion H7N9 influenza vaccine in a mouse model. Mice were immunized intramuscularly once with different doses of inactivated whole-virion H7N9 influenza vaccine alone or in combination with MF59 adjuvant. Specific IgM and IgG antibody titers in sera of mice were detected by ELISA 3, 5 and 7days after immunization. To evaluate the early protection provided by the vaccine, mice were challenged with lethal dose (40LD 50 ) of homologous virus 3, 5 and 7 days after immunization respectively. The survival rate and body weight change of mice during 21 days after challenge and the residual lung virus titer on 3rd day after challenge were determined. The results demonstrated that mice could obtain effective protection 3 days after immunization with the vaccine at a high dose, and 5–7 days after immunization even at a low dose. Thus early immune responses induced by inactivated whole-virion H7N9 vaccine could provide effective protection.
机译:摘要H7N9人类流感感染会导致严重的呼吸道疾病。疫苗接种是预防流感病毒的最佳方法。在本文中,我们研究了在小鼠模型中灭活的全部病毒虫H7N9流感疫苗提供的早期保护的影响。用不同剂量的灭活的全部病毒素H7N9流感疫苗单独或与MF59佐剂组合使用不同剂量的颗粒中的肌肉内肌肉内免疫。免疫后,通过ELISA 3,5和7ds检测小鼠血清中的特异性IgM和IgG抗体滴度。为了评估疫苗提供的早期保护,小鼠分别与免疫后的同源病毒3,5和7天的致命剂量(40LD 50)攻击。确定了攻击后21天后小鼠的存活率和体重变化和攻击后第3天的残留肺病毒滴度。结果表明,小鼠在用高剂量的疫苗免疫后3天可以获得有效的保护,并且在免疫后5-7天甚至在低剂量后免疫。因此,由灭活的全部病毒虫H7N9疫苗引起的早期免疫应答可以提供有效的保护。

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