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. 2010 Mar 31;354(1-2):68–79. doi: 10.1016/j.jim.2010.02.002

Fig. 2.

Fig. 2

Impact of polyclonal expansion on T cell memory phenotype in blood. Representative plots showing (A) naive and antigen-experienced cells (total memory) based on differential staining with CD27 and CD45RO; and (B) differentiation markers expression (CD45RO, CD27, and CCR7) on CD8+ T cells from blood. Eight distinct memory subsets were defined from these markers: Central memory cells, (CD45RO+CD27+CCR7+), transitional memory cells (CD45RO+CD27+CCR7), effector memory cells (CD45RO+CD27+CCR7+), CD45RO+CD27CCR7+, naive T cells (CD45ROCD27+CCR7+), intermediate memory cells (CD45ROCD27+CCR7), effector (CD45ROCD27CCR7) and CD45ROCD27CCR7cells. (C) Comparison of the frequency of total, effector memory and central memory subsets expressed as percentages of total CD4+ and CD8+ T cells in chronically HIV-infected individuals (n = 5) before and after expansion using seven different protocols. Each box and whisker plot shows the median (central line), IQR (outer lines of box) and 5–95% range (error bars) of 5 HIV-infected individuals. * indicates p < 0.05 while ** indicates p < 0.01 using Wilcoxon rank test.