Cold immunolabeling combined with negative staining (GINS) provides a valua
ble immunocytochemical approach that allows a direct ultrastructural defini
tion of all viral vaccine constituents that share common antigenic features
with pathogenic viral particles. These results have implications for the d
evelopment of viral vaccines since it has been demonstrated that incomplete
viral particles such as natural empty capsides and Rotavirus-like particle
s lacking the infective genome are potential candidates for the production
of neutralizing antibodies. Furthermore comparative results of the applicat
ion of GINS to either inactivated vaccines or unfixed samples provide direc
t evidence that even after inactivation specific antigenic sites are still
available for gold immunolabeling. (C) 2001 Academie des sciences/Editions
scientifiques et medicales Elsevier SAS.