The epitope stability of a varicella-zoster virus (VZV) glycoprotein E (gE)
was analyzed with monoclonal antibodies (mAbs) in cells infected with diff
erent passages of various VZV strains and isolates. The gE-specific mAbs re
cognized same antigenic sites (epitopes) in VZV isolates with various passa
ge history. All VZV strains and virus-isolates reacted with an anti-gE mono
clonal antibody by immunoprecipitation, or indirect fluorescent antibody st
aining test. Sera from VZV seropositive individuals reacted with a truncate
d VZV gE glycoprotein, designated TgpI-511. Also, human mononuclear cells (
MNCs) stimulated with TgpI-511 glycoprotein were shown to produce VZV-speci
fic antibodies in vitro. The results demonstrated the stability of these gE
epitopes tested in this study in TgpI-511 and among the VZV-isolates obtai
ned from different passages. These results also suggest that VZV glycoprote
ins as well as live attenuated or killed varicella vaccines containing thes
e epitopes could be used as therapeutic booster vaccines in adults and the
elderly to prevent tester.