Ten million syngeneic hepatocellular carcinoma (FAA-HTC1) cells inject
ed into liver are sufficient to kill Fischer rats within 2 months, Fis
cher rats became resistant to FAA-HTC1 cells by repeated sensitization
with MMC-treated FAA-HTC1 cells. Histopathological studies revealed m
assive accumulation of mononuclear cells in tumor tissues of sensitize
d rats that were rejecting syngeneic FAA-HTC1 cells, whereas very few
mononuclear cells were found in tumor tissues of control rats. Cell po
pulations infiltrating the tumor tissues were identified by immunohist
ochemical techniques and flow cytometric analysis. Mononuclear cells f
ound within the regressing tumors of the sensitized rats were mostly i
dentified as being T cells, and two-thirds of these T cells were CD8 p
ositive. Compared to control rats, killer activity of mononuclear cell
s infiltrating tumor tissues was significantly increased in the sensit
ized rats. Depletion of CD8(+) T cells significantly reduced the cytot
oxic ability of mononuclear cells infiltrating tumors obtained from se
nsitized rats. In contrast, depletion of CD16(+) cells significantly r
educed the cytotoxic ability of mononuclear cells infiltrating tumors
obtained from control rats.