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. 2011 Nov 19;18(2):479–489. doi: 10.1007/s12253-011-9471-y

Fig. 1.

Fig. 1

CD28 expression in peripheral blood CD8+ T cells from patients with CC and from healthy controls before and after 24 h, 48 h and 72 h stimulation with anti-CD3 MoAb + rIL-2. The dot plots and histograms show representative data, illustrating the analysis method for identification of CD3+/CD8+ cells expressing CD28 following three-color staining. (a) The dot plots show the forward scatter/side scatter (FSC/SSC) distribution and the gate (region R1) was used to select lymphocytes for analysis. The R1 gated events were then analyzed for CD3/PerCP and CD8/FITC staining and double-positive cells (CD3 + CD8+) were gated (region R2). The dot plots show representative data from one patient with CC. (b) The final histograms. The double-gated populations were then analyzed for CD28/RPE. The gray histograms represent the isotype controls. The numbers located on the histograms represent the percentage of CD3 + CD8+ cells expressing CD28 molecule