The majority of human hepatocellular carcinomas overexpress alpha-fetoprote
in (AFP), Two genetic immunization strategies were used to determine whethe
r AFP could serve as a target for T-cell immune responses. Dendritic cells
engineered to express AFP produced potent T-cell responses in mice, as evid
enced by the generation of AFP-specific CTLs, cytokine-producing T cells, a
nd protective immunity. AFP plasmid-based immunization generated less poten
t responses, These novel observations demonstrate that this oncofetal antig
en can serve as an effective tumor rejection antigen. This provides a ratio
nal, gene therapy-based strategy for this disease, which is responsible for
the largest number of cancer-related deaths worldwide.