IL-5 is generally regarded as a Th2 cytokine involved in eosinophil maturat
ion and function and in B cell growth and antibody production, but without
any well-established effects on T cells. Early reports suggested that IL-5
could stimulate the production of cytotoxic T lymphocytes (CTL) in vitro, b
ut no evidence has been obtained to date for such a role in studies with IL
-5-deficient (IL-5(-/-)) mice. Here we demonstrate that when oxidized manna
n MUC1 fusion protein (M-FP) is used as an antigen in mice, IL-5 is require
d for the optimal generation of the CTL response. IL-5 was as effective as
IL-2 for the induction of CTL from spleen cells in vitro and both CD4(+) an
d CD8(+) T cells from M-FP-immunized animals could be shown to secrete IL-5
in culture, in IL-5(-/-) mice, CTLp frequency was greatly diminished resul
ting in the inability to reject MUC1(+) tumors. Clearly, IL-5 is produced b
y functional T cells, especially the Tc1 type, after M-FP immunization and
is required for an optimal CTL response to this antigen.