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比较一系列表达病毒蛋白的质粒DNA预防H5N1流感病毒感染的能力。

Comparing the ability of a series of viral protein-expressing plasmid DNAs to protect against H5N1 influenza virus.

作者信息

Chen Quanjiao, Kuang Haimen, Wang Huadong, Fang Fang, Yang Zhongdong, Zhang Zhiping, Zhang Xianen, Chen Ze

机构信息

State Key Laboratory of Virology, Wuhan Institute of Virology, Chinese Academy of Sciences, Wuhan, Hubei, 430071, China.

出版信息

Virus Genes. 2009 Feb;38(1):30-8. doi: 10.1007/s11262-008-0305-2. Epub 2008 Dec 10.

Abstract

Avian influenza has been regarded as a human health threat. A major measure to prevent its outbreak is vaccination. In this study, a series of expression plasmids carrying the hemagglutinin (HA), neuraminidase (NA), nucleoprotein (NP), matrix protein 1 (M1), and matrix protein 2 (M2) genes, respectively, of the avian influenza virus (AIV) A/Chicken/Henan/12/2004(H5N1) strain were constructed. These plasmids were administered to mice by electroporation (50 mug for each per administration, 1-5 times, at an interval of 2 weeks), and the mice were challenged with the homologous virus later. The mice immunized with HA plasmid once and the NA plasmid twice survived 100%, and those with NP plasmid showed 60-80% survival rate with at least three immunizations. The mice immunized with M1 plasmid survived 25% with five immunizations, while M2 plasmid had no protection even with five immunizations. The mixture of M1 and NP plasmids protected 95% of the mice against the homologous virus, and 80% of the mice against a challenge with heterologous H1N1 (PR8) virus. Moreover, the homologous protection lasted at least 6 months. Our data provided a basis for selecting multiple-component AIV vaccines.

摘要

禽流感已被视为对人类健康的威胁。预防其爆发的一项主要措施是接种疫苗。在本研究中,构建了一系列分别携带禽流感病毒(AIV)A/Chicken/Henan/12/2004(H5N1)株血凝素(HA)、神经氨酸酶(NA)、核蛋白(NP)、基质蛋白1(M1)和基质蛋白2(M2)基因的表达质粒。通过电穿孔法将这些质粒给予小鼠(每次每只50微克,共1 - 5次,间隔2周),随后用同源病毒对小鼠进行攻毒。单次接种HA质粒和两次接种NA质粒的小鼠100%存活,至少接种三次NP质粒的小鼠存活率为60% - 80%。五次接种M1质粒的小鼠存活率为25%,而即使五次接种M2质粒也没有保护作用。M1和NP质粒的混合物可保护95%的小鼠抵御同源病毒,80%的小鼠抵御异源H1N1(PR8)病毒的攻毒。此外,同源保护作用至少持续6个月。我们的数据为选择多组分禽流感疫苗提供了依据。

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