To investigate the precise role of antigen-specific Th1 and Th2. cells in t
umor immunity, we developed a novel adoptive tumor-immunotherapy model usin
g OVA-specific Th1 and Th2 cells and an OVA gene-transfected tumor. This th
erapeutic model demonstrated that both antigen-specific Th1 and Th2 cells h
ad strong antitumor activity in vivo with distinct mechanisms. However, imm
unological memory suitable for the generation of tumor-specific cytotoxic T
lymphocytes was induced only when tumor-bearing mice received Th1 cell the
rapy, but not Th2 cell therapy. Thus it was strongly suggested that Th1-dom
inant immunity is critically important for the induction of antitumor cellu
lar immunity in vivo. We also proposed that several immunomodulating protoc
ols using interleukin (IL)-12, IL-12 gene, the natural killer T cell ligand
alpha-galactosylceramide, or Th1 cytokine-conditioned dendritic cells migh
t be useful strategies for the induction of Th1-dominant immunity essential
for the development of tumor-specific immunotherapy.