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. 1999 Mar;96(3):358–364. doi: 10.1046/j.1365-2567.1999.00712.x

Figure 1.

Figure 1

The expression of IFN-γ and IL-4 by PB and SF CD4+ and CD8+ T cells. PBMC or SFMC were activated for 5 hr in the presence or absence of PMA (10 ng/ml)+ ionomycin (0·5 μg/ml), or anti-CD3 mAb (1 μg/ml)+ anti-CD28 mAb (10 μg/ml). Brefeldin A (10 μg/ml) was added to the cultures to prevent cytokine secretion. Activated cells were stained with PerCP-conjugated anti-CD4 or anti-CD8 mAb, fixed, permeabilized in 0·1% saponin and stained with FITC-conjugated anti-human IFN-γ and PE-conjugated anti-human IL-4 mAb. CD4+ or CD8+ cells were gated and quadrants were set on the basis of FITC- and PE-conjugated IgG1 isotype controls. The values denote the percentage of cells in each quadrant.