Ertl H C, Dietzschold B, Gore M, Otvos L, Larson J K, Wunner W H, Koprowski H
Wistar Institute of Anatomy and Biology, Philadelphia, Pennsylvania 19104-4268.
J Virol. 1989 Jul;63(7):2885-92. doi: 10.1128/JVI.63.7.2885-2892.1989.
The T-helper cell response to the internal proteins of rabies virus was investigated. The rabies virus nucleoprotein was shown to be a major target antigen for T-helper cells that cross-react between rabies and rabies-related viruses. T-helper cells were assayed in vitro by testing virus-induced lymphocytes for lymphokine secretion in response to antigen. Immunodominant T-helper cell epitopes of the viral nucleoprotein were identified in vitro by using synthetic peptides delineated from the amino acid sequence of the nucleoprotein. The response to synthetic peptides were under Ir gene control. Antigenic peptides were tested in vivo for stimulation of rabies virus-specific T-helper cells. Inoculation of mice with peptides bearing immunodominant T-helper cell epitopes resulted in an accelerated and enhanced neutralizing antibody response upon booster immunization with inactivated rabies virus.
研究了辅助性T细胞对狂犬病病毒内部蛋白的反应。狂犬病病毒核蛋白被证明是辅助性T细胞的主要靶抗原,这些辅助性T细胞在狂犬病病毒和狂犬病相关病毒之间发生交叉反应。通过检测病毒诱导的淋巴细胞对抗原刺激后的淋巴因子分泌,在体外对辅助性T细胞进行测定。利用从核蛋白氨基酸序列中划定的合成肽,在体外鉴定了病毒核蛋白的免疫显性辅助性T细胞表位。对合成肽的反应受Ir基因控制。在体内测试了抗原肽对狂犬病病毒特异性辅助性T细胞的刺激作用。用带有免疫显性辅助性T细胞表位的肽接种小鼠,在用灭活狂犬病病毒加强免疫后,中和抗体反应加快且增强。