Cytotoxic T lymphocytes (Tc) play a central role in cellular immunity again
st cancers. The cytotoxic potential of freshly isolated tumor-infiltrating
lymphocytes (TILs) is usually not expressed. This suggests the possible exi
stence of as yet unspecified and perhaps complex immunosuppressive factors
or cytokines that affect the anti-tumor capacity of these TILs in the tumor
milieu. In the present study, we demonstrated for the first time that TILs
derived from human cervical cancer tissue consist mainly of Th2/Tc2 phenot
ypes. In vitro kinetic assays further revealed that cancer cells could dire
ct the tumor-encountered T cells toward the Th2/Tc2 polarity. Cancer cells
promote the production of IL-4 and down-regulate the production of IFN-gamm
a in cancer-encountered T cells. The regulatory effects of cervical cancer
cells are mediated mainly by IL-10, and TGF-beta plays only a synergistic r
ole. The cancer-derived effects can be reversed by neutralizing anti-IL-10
and anti-TGF-beta Abs. IL-10 and TGF-beta are present in cancer tissue and
weakly expressed in precancerous tissue, but not in normal cervical epithel
ial cells. Our study strongly suggests important regulatory roles of IL-10
and TGF-beta in cancer-mediated immunosuppression.