Bot A, Bot S, Bona C
Department of Microbiology, Mount Sinai School of Medicine, New York, NY 10029, USA.
Vaccine. 1998 Oct;16(17):1675-82. doi: 10.1016/s0264-410x(98)00054-1.
Effective immunization of neonates is an important goal for vaccinology. We show that inoculation of newborn mice with a mixture of plasmids expressing influenza hemagglutinin (HA) and nucleoprotein (NP) genes leads to an enhanced protection subsequent to the lethal challenge with two distinct strains. In sharp contrast, neonatal injection with UV-inactivated influenza virus strain WSN, failed to induce protection against the homologous challenge. Our results show that while plasmid immunization of neonates elicits a protective immunity, the immunization with inactivated virus does not.
新生儿的有效免疫是疫苗学的一个重要目标。我们发现,用表达流感血凝素(HA)和核蛋白(NP)基因的质粒混合物接种新生小鼠,在受到两种不同毒株的致死性攻击后可增强保护作用。与之形成鲜明对比的是,用紫外线灭活的流感病毒株WSN对新生儿进行注射,未能诱导出针对同源攻击的保护作用。我们的结果表明,虽然新生儿进行质粒免疫可引发保护性免疫,但用灭活病毒进行免疫则不能。