Dendritic cells (DCs) generated in vitro from bone marrow precursors using
granulocyte-macrophage colony-stimulating factor (GM-CSF) secrete interleukin-2
(IL-2) upon activation, an event probably associated to the initiation of adaptive
immune responses. Additionally, they produce IL-12, a cytokine related to T-cell
polarization. To analyse the effect of IL-4 on DC differentiation and function, we
assessed the capacity of murine bone marrow dendritic cells (BMDCs) differentiated with GM-CSF in the presence or absence of IL-4 to produce IL-2 and
IL-12 upon lipopolysaccharide (LPS) activation. We found that although IL-4
enhanced DC IL-12p70 production, it strongly impaired IL-2 secretion by
BMDCs. This inhibition, which depends on the presence of IL-4 during LPS
activation, is DC specific, as IL-4 did not affect IL-2 secretion by T cells.
Interestingly, inhibition of DC IL-2 production did not prevent DC priming of
T lymphocytes. These results illustrate a new putative role for IL-4 on the
regulation of the immune response and should help clarify the controversial
reports on the effect of IL-4 on DCs.