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. 1999 Nov 15;190(10):1439–1450. doi: 10.1084/jem.190.10.1439

Figure 3.

Figure 3

Instruction for IL-4 expression after primary activation of Th lymphocytes. Naive CD62L+CD4+ OVA-TCRtg/tg cells were either directly stimulated with PMA/ionomycin or they were labeled with CFSE and activated for 17 or 42 h with OVA323–339 and APCs in the presence of IL-4, anti–IL-12, and anti–IFN-γ before PMA/ionomycin recall. Intracellular IL-4 and IL-2 expression were examined among OVA-TCR+ cells. The specificity of the intracellular IL-4 staining was controlled by blocking the digoxigenized anti–IL-4 detection mAb with an excess of the unconjugated anti–IL-4 mAb. Indicated frequencies of IL-2–producing cells have been corrected for the background frequencies of the respective control stainings.