In mice infected with the non‐lethal malaria parasite Plasmodium chabaudi chabaudi AS, a prominent switch from a Th1 to a Th2 type of response occurs in CD4⁺ T cells at the time of peak parasitemia or shortly thereafter (9 – 15 days after infection). This is accompanied by a major increase in IL‐4, and a similar decrease in IFN‐γ‐producing cells. Non‐B‐non‐T cells have been shown to be the main source of the IL‐4 in these mice. The IL‐4‐producing cells are hyperresponsive to IL‐3, indicating mast cell or basophil origin. To further characterize this cell population we have studied various organs at different time points of malarial infection by Northern blot analysis. No significant increase in the expression of any of the classical mouse mast cell serine proteases (MMCP)‐1 to 7 or carboxypeptidase A was detected in the spleen during the entire infection. However, a marked increase in the expression of MMCP‐8 was observed in the spleen at around day 15 post infection. Isolation of IgE receptor‐positive cells from spleen shortly after peak parasitemia led to a prominent enrichment of MMCP‐8‐expressing cells. Fifty thousand of these cells were, after IL‐3 stimulation, found to produce IL‐4 to levels comparable with more than one million fully activated T cells. Our results show that basophil‐like cells are very potent producers of IL‐4 and that IL‐4 produced by these cells may be of major importance for the initiation of a Th2 response. In addition, the detection of MMCP‐8 in these cells has led to the identification of the first basophil‐specific differentiation marker in the mouse.