Robinson H L, Boyle C A, Feltquate D M, Morin M J, Santoro J C, Webster R G
Department of Pathology, University of Massachusetts Medical Center, Worcester 01655, USA.
J Infect Dis. 1997 Aug;176 Suppl 1:S50-5. doi: 10.1086/514176.
DNA-based immunizations have been used to analyze the ability of DNA-expressed hemagglutinin (HA) and nucleoprotein (NP) to protect BALB/c mice against a homologous influenza virus, A/PR/8/34 (H1N1), challenge. The HA DNA, but not the NP DNA, protected mice against the lethal viral challenge. For the HA DNA, single gene gun inoculations of 0.04 microg and boosted inoculations of 0.004 microg of DNA raised complete protection. For the NP DNA, boosted gene gun immunizations of 0.4 microg of DNA and boosted intradermal or intramuscular injections of 50 microg of DNA failed to protect. The protection elicited by the HA DNA vaccine correlated with the titers of neutralizing antibody.
基于DNA的免疫接种已被用于分析DNA表达的血凝素(HA)和核蛋白(NP)保护BALB/c小鼠免受同源流感病毒A/PR/8/34(H1N1)攻击的能力。HA DNA而非NP DNA可保护小鼠免受致死性病毒攻击。对于HA DNA,单次基因枪接种0.04微克DNA以及加强接种0.004微克DNA可产生完全保护。对于NP DNA,加强基因枪免疫接种0.4微克DNA以及加强皮内或肌肉注射50微克DNA均未能起到保护作用。HA DNA疫苗引发的保护作用与中和抗体滴度相关。