Ray N B, Ewalt L C, Lodmell D L
Laboratory of Persistent Viral Diseases, Rocky Mountain Laboratories, National Institute of Allergy and Infectious Diseases, Hemilton, MT 59840, USA.
Vaccine. 1997 Jun;15(8):892-5. doi: 10.1016/s0264-410x(96)00281-2.
Vaccination against virus infections has proven to be an effective strategy in the improvement of human health. In this study, we evaluated two plasmid DNA vaccines expressing the glycoprotein (G) gene of the challenge virus standard (CVS) rabies virus for their ability to elicit neutralizing antibody and protect BALB/cByJ mice against lethal rabies virus challenge. A single inoculation of 10 micrograms of plasmid DNA encoding G protected 100% of the intramuscularly (i.m.) vaccinated mice, and 0.1 microgram of DNA protected 83% of the intradermally (i.d.) vaccinated mice. All mice that survived had serum anti-rabies virus neutralizing antibody titers > or = 1:40 prior to virus challenge. The highest antibody titers were detected in mice that had been inoculated i.m. with 10-100 micrograms of DNA in regenerating muscle. The immunostimulant monophosphoryl lipid A enhanced the neutralizing antibody response of i.d.-vaccinated mice. Anti-rabies virus neutralizing antibody elicited by plasmid DNA vaccination cross-neutralized a global spectrum of rabies virus variants. These results indicate that DNA vaccines could be a solution for providing developing countries with an inexpensive vaccine that is simple to prepare, is highly efficacious and has excellent stability.
事实证明,针对病毒感染进行疫苗接种是改善人类健康的有效策略。在本研究中,我们评估了两种表达狂犬病病毒攻击病毒标准株(CVS)糖蛋白(G)基因的质粒DNA疫苗,它们引发中和抗体以及保护BALB/cByJ小鼠抵御致死性狂犬病病毒攻击的能力。单次接种10微克编码G的质粒DNA可保护100%经肌肉注射(i.m.)接种疫苗的小鼠,而0.1微克DNA可保护83%经皮内注射(i.d.)接种疫苗的小鼠。所有存活的小鼠在病毒攻击前血清抗狂犬病病毒中和抗体滴度均≥1:40。在经再生肌肉肌肉注射10 - 100微克DNA的小鼠中检测到最高抗体滴度。免疫刺激剂单磷酰脂质A增强了经皮内接种疫苗小鼠的中和抗体反应。质粒DNA疫苗引发的抗狂犬病病毒中和抗体可交叉中和全球范围内的狂犬病病毒变种。这些结果表明,DNA疫苗可能为发展中国家提供一种廉价疫苗,这种疫苗制备简单、高效且稳定性极佳。