Dix R D
Department of Ophthalmology, University of Miami School of Medicine, Bascom Palmer Eye Institute, Florida 33101.
J Med Virol. 1990 Mar;30(3):192-5. doi: 10.1002/jmv.1890300309.
Four monoclonal antibodies directed against glycoprotein B of herpes simplex virus were evaluated for their ability to immunize mice passively against acute virus-induced neurological illness and death when administered intraperitoneally 2 hours prior to footpad challenge with type 1 or type 2 virus. Two monoclonal antibodies, H120 and H157, failed to reduce the severity of neurological disease in infected animals. In contrast, H233 and H368 antibodies provided significant protection in type-common and type-specific fashions, respectively. A direct correlation was observed between in vitro neutralization and in vivo protection. These results provide the first in vivo evidence that glycoprotein gB of herpes simplex virus expresses both type-common and type-specific determinants during the evolution of acute virus-induced neurological disease.
在以1型或2型病毒对小鼠足垫进行攻击前2小时腹腔注射4种针对单纯疱疹病毒糖蛋白B的单克隆抗体,评估其被动免疫小鼠抵抗急性病毒诱导的神经疾病和死亡的能力。两种单克隆抗体H120和H157未能减轻感染动物神经疾病的严重程度。相比之下,H233和H368抗体分别以共同型和特定型方式提供了显著保护。体外中和作用与体内保护作用之间存在直接相关性。这些结果提供了首个体内证据,表明单纯疱疹病毒糖蛋白gB在急性病毒诱导的神经疾病演变过程中表达共同型和特定型决定簇。