Chen Z, Kadowaki S, Hagiwara Y, Yoshikawa T, Matsuo K, Kurata T, Tamura S
Department of Pathology, National Institute of Infectious Diseases, Toyama 1-23-1, Shinjuku-ku, 162-8640, Tokyo, Japan.
Vaccine. 2000 Aug 1;18(28):3214-22. doi: 10.1016/s0264-410x(00)00149-3.
Cross-protection against a lethal influenza virus infection was examined in BALB/c mice immunized with plasmid DNAs encoding the neuraminidase (NA) from different subtype A viruses. Each NA-DNA was administered twice, 3 weeks apart, at the 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 lethal doses of homologous or heterologous viruses and the ability of each NA-DNA to protect the mice from influenza was evaluated by determining the lung virus titers, body weight and survival rates. The H3N2 virus NA-DNA conferred cross-protection against lethal challenge with antigenic variants within the same subtype, but failed to provide protection against infection by a different subtype virus (H1N1). The degree of cross-protection against infection was related to titers of the cross-reacting antibodies. These results suggest that NA-DNA can be used as a vaccine component to provide effective protection against infection not only with homologous virus but also with drift viruses.
在用编码来自不同甲型病毒亚型神经氨酸酶(NA)的质粒DNA免疫的BALB/c小鼠中,检测了对致死性流感病毒感染的交叉保护作用。每种NA-DNA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,用致死剂量的同源或异源病毒攻击小鼠,并通过测定肺病毒滴度、体重和存活率来评估每种NA-DNA保护小鼠免受流感感染的能力。H3N2病毒NA-DNA对同一亚型内的抗原变异体的致死攻击具有交叉保护作用,但不能提供针对不同亚型病毒(H1N1)感染的保护。针对感染的交叉保护程度与交叉反应抗体的滴度有关。这些结果表明,NA-DNA可作为疫苗成分,不仅能有效保护免受同源病毒感染,还能抵御漂移病毒感染。