Caselli E, Grandi P, Argnani R, Balboni P G, Selvatici R, Manservigi R
Department of Experimental and Diagnostic Medicine (Section of Microbiology), University of Ferrara, Italy.
Intervirology. 2001;44(1):1-7. doi: 10.1159/000050023.
Intramuscularly (i.m.) delivered plasmid DNA encoding a secreted form of glycoprotein B of herpes simplex virus type 1 (HSV-1 gB1s) was evaluated for the ability to elicit a protective immune response in Balb/c mice. Animals received three i.m. injections of a gB1s expression plasmid (pRP-RSV-gB1s) or of a wild-type transmembrane gB1 coding plasmid (pRP-RSV-gB1), while control mice were injected with the vector alone (pRP-RSV). A specific antibody response was observed in almost all immunized animals, and in most cases antibodies were also detected after 1 month in the absence of further vaccine boosts. Serum antibodies mostly displayed neutralizing activity against HSV-1. Glycoprotein B1s DNA immunization was also effective in protecting animals against the primary infection induced by a subsequent HSV-1 challenge and limited HSV-1 infection of sensitive ganglia.
对肌肉注射编码1型单纯疱疹病毒糖蛋白B分泌形式(HSV-1 gB1s)的质粒DNA在Balb/c小鼠中引发保护性免疫反应的能力进行了评估。动物接受了三次肌肉注射gB1s表达质粒(pRP-RSV-gB1s)或野生型跨膜gB1编码质粒(pRP-RSV-gB1),而对照小鼠仅注射载体(pRP-RSV)。在几乎所有免疫动物中均观察到特异性抗体反应,并且在大多数情况下,在没有进一步疫苗加强接种的情况下,1个月后也检测到了抗体。血清抗体大多表现出对HSV-1的中和活性。糖蛋白B1s DNA免疫在保护动物免受随后HSV-1攻击诱导的原发性感染以及限制敏感神经节的HSV-1感染方面也有效。