Chen Z, Kadowaki S, Hagiwara Y, Yoshikawa T, Sata T, Kurata T, Tamura S
Department of Pathology, National Institute of Infectious Diseases, Toyama 1-23-1, Shinjuku-ku, 162-8640, Tokyo, Japan.
Vaccine. 2001 Jan 8;19(11-12):1446-55. doi: 10.1016/s0264-410x(00)00351-0.
Protection against a lethal influenza B virus infection was examined in BALB/c mice immunized with plasmid DNAs encoding hemagglutinin (HA), neuraminidase (NA and NB) and nucleoprotein (NP) from the B/Ibaraki/2/85 virus. Each DNA vaccine was administered twice, 3 weeks apart, at a dose of 1 microg per mouse by particle-mediated DNA transfer to the epidermis (gene gun) or at a dose of 30 microg per mouse by electroporation into the muscle. Three weeks after the second vaccination, the mice were challenged with a lethal dose of homologous virus. HA and NA DNAs conferred complete protection against the lethal viral challenge, whereas NB and NP DNAs failed to provide protection against infection. Furthermore, protection in different strains of mice, BALB/c, B10 and C3H, immunized with HA and NA DNAs was compared. Both HA and NA DNAs conferred complete protection against the lethal challenge in all the tested mouse strains. These results suggest that both the HA and NA molecules can be used as vaccine components to provide effective protection against influenza B virus infection.
在用编码来自B/茨城/2/85病毒的血凝素(HA)、神经氨酸酶(NA和NB)和核蛋白(NP)的质粒DNA免疫的BALB/c小鼠中,检测了对致死性乙型流感病毒感染的保护作用。每种DNA疫苗通过粒子介导的DNA转移至表皮(基因枪)以每只小鼠1微克的剂量或通过电穿孔导入肌肉以每只小鼠30微克的剂量,间隔3周给药两次。第二次接种后3周,用致死剂量的同源病毒攻击小鼠。HA和NA DNA对致死性病毒攻击提供了完全保护,而NB和NP DNA未能提供针对感染的保护。此外,比较了用HA和NA DNA免疫的不同品系小鼠(BALB/c、B10和C3H)中的保护作用。HA和NA DNA在所有测试的小鼠品系中均对致死性攻击提供了完全保护。这些结果表明,HA和NA分子均可用作疫苗成分,以提供针对乙型流感病毒感染的有效保护。