Interleukin (IL)-4 has an important role in regulating antibody production
and inflammation. The major IL-4 producers are CD4(+) T cells, but the deve
lopment of an IL-4-producing phenotype in these cells requires IL-4 signali
ng through the STAT6 pathway during differentiation. The cellular source of
this early IL-4 is not known, but mast cells are a possible candidate due
to their immediate and indiscriminate release of IL-4 upon activation. In t
his review we summarize the evidence that STATE signaling is not required f
or mast cell IL-4 production, which is consistent with their possible role
as a link between the innate immune response and T-cell activation. We also
describe an isoform of STATE that is expressed in mast cells and that appe
ars to act as a repressor of IL-4 transcription. This STAT6 signaling pathw
ay may be part of a feedback mechanism to protect surrounding tissues from
IL-4-mediated inflammation during an infection.