Recent studies indicate that a large proportion of cytotoxic T cells are di
rected towards the Epstein-Barr virus (EBV) during both acute infection and
convalescence. The virus, in turn, has usurped cellular pathways to promot
e proliferation of infected cells and has pirated cellular genes into its g
enome to modulate the immune system to allow lifelong infection of humans.
Analysis of the immune response to the virus is leading to novel therapies
for EBV-associated malignancies, including the use of virus-specific cytoto
xic T cell infusions.