The efficacy of a recombinant vaccinia virus (rvv-GM-CSF) expressing the gr
anulocyte macrophage colony stimulating factor (GM-CSF) as tumor vaccine wa
s evaluated in the murine B16-F10 melanoma model. The vaccine was prepared
by infection of irradiated tumor cells with rvv-GM-CSF. Control vaccine was
B-16 cells infected with a recombinant vaccinia virus expressing Escherich
ia coli beta-galactosidase (rvv-lacZ), Pre-vaccination of naive C57BL/6 mic
e later inoculated with tumor cells and treatment of mice bearing armors wi
th GM-CSF vaccine inhibited tumor. development and prolonged survival. Lung
metastasis of B-16 was also inhibited by treatment with GM-CSF vaccine. Th
e vaccine effects appeared to be tumor cell specific. The efficacy of the v
accine was comparable to a retroviral vaccine (MFG-muGM-CSF) in this system
. The vaccine was also effective when rvv-GM-CSF was directly injected into
the tumor: These data suggest that this vaccine approach has potential for
use in cancer treatment, especially for patients with easily accessible tu
mors.