Fig. 4.
Fig. 4. Phenotypic features of CD4lo cells. / CD4lo cells show phenotypic features of activated T lymphocytes. (A) CD3 expression on CD4lo cells is lower than on CD4+ and CD4− T cells. Bar graph of mean fluorescence intensities (mean ± SEM, n = 27) of peripheral blood lymphocytes stained with Cychrome–anti-CD4 and FITC–anti-CD3 and analyzed after setting up the regions as in a representative density plot (A inset, R1-CD4+, R2-CD4lo). Statistically significant (paired ttest) differences were observed between the FITC-CD3 fluorescence intensities of CD4lo cells (▪) and CD4+lymphocytes (░; *P = .022) and between CD4loand CD3− cells (■; ***P = .00004). (B-C) Lowered expression of CD4 is associated with high expression of activation antigens CD25 and HLA-DR (B and C insets show representative density plots). Bar graph in panel B shows statistically significant difference between the expression of CD4 on cells from the R2 region of the inset expressing CD25 (□) and the CD25− T cells from region R1 (▪) (*mean ± SEM, n = 5, P = .0001). Panel C shows a similar difference between HLA-DR+ (■) and HLA-DR− cells (▪; *mean ± SEM, n = 5,P = .0001). (D) The proportion of CD4lo and CD4+ cells expressing CD45RA antigen was similar (bar graph), but the intensity of its expression was higher on CD4lo cells (inset).

Phenotypic features of CD4lo cells.

CD4lo cells show phenotypic features of activated T lymphocytes. (A) CD3 expression on CD4lo cells is lower than on CD4+ and CD4 T cells. Bar graph of mean fluorescence intensities (mean ± SEM, n = 27) of peripheral blood lymphocytes stained with Cychrome–anti-CD4 and FITC–anti-CD3 and analyzed after setting up the regions as in a representative density plot (A inset, R1-CD4+, R2-CD4lo). Statistically significant (paired ttest) differences were observed between the FITC-CD3 fluorescence intensities of CD4lo cells (▪) and CD4+lymphocytes (░; *P = .022) and between CD4loand CD3 cells (■; ***P = .00004). (B-C) Lowered expression of CD4 is associated with high expression of activation antigens CD25 and HLA-DR (B and C insets show representative density plots). Bar graph in panel B shows statistically significant difference between the expression of CD4 on cells from the R2 region of the inset expressing CD25 (□) and the CD25 T cells from region R1 (▪) (*mean ± SEM, n = 5, P = .0001). Panel C shows a similar difference between HLA-DR+ (■) and HLA-DR cells (▪; *mean ± SEM, n = 5,P = .0001). (D) The proportion of CD4lo and CD4+ cells expressing CD45RA antigen was similar (bar graph), but the intensity of its expression was higher on CD4lo cells (inset).

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