IL-4 in combination with TGF-β favors an alternative pathway of Th1 development independent of IL-12

IL-4 was found to be the essential differentiation factor for Th2 cells and simultaneously to be a potent inhibitor of Th1 development that is induced by IFN-gamma and IL-12, Furthermore, it was demonstrated that TGF-beta can also inhibit Th1 development, In this work, we demonstrate that polyclonal activation of Mel-14(high)CD4(+) T cells by immobilized anti-alpha beta TCR mAb together with a mixture of IL-4 and TGF-P can lead to the development of both Th1 and Th2 cells, depending on the concentration of these cytokines, Additional experiments revealed that Th1 induction by a combination of IL-4 and TGF-beta depends on the presence of endogenous IFN-gamma and that this alternative Th1 development is further enhanced by IL-12, but is not dependent on this cytokine. Moreover, naive OVA(323-339)-specific Th cells that were stimulated by APCs and OVA(323-339) peptide differentiated toward Th1 cells after priming in the presence of IL-4 in combination with TGF-beta. Hence, this finding confirmed the results obtained by polyclonal activation of naive CD4(+) Th cells and implicates that this alternative Th1 development may also occur in vivo under the influence of TGF-beta and IL-4 independently of the Th1-promoting effect of IL-12.