Figure 3
Figure 3. CD25 and CD71 are highly expressed on alloreactive T cells. (A) Kinetics of surface marker and cytokine expression in proliferating alloreactive T cells (n = 5). Normal donor PBMCs were cocultured with HLA-mismatched DCs, and the expression of surface markers and intracellular cytokines in the proliferating alloreactive T-cell population was determined by gating on the CFSEdim population using FACS analysis. Data shown are means ± SD. (B) CD71 is highly expressed in proliferating CD25− alloreactive T cells (n = 5). CFSE labeled T cells were cocultured with HLA-mismatched DCs, and the kinetics of expression of surface markers and intracellular cytokines in the proliferating alloreactive CD25− population were determined flow cytometrically by gating on the CFSEdimCD25− cells. Results are means ± SD.

CD25 and CD71 are highly expressed on alloreactive T cells. (A) Kinetics of surface marker and cytokine expression in proliferating alloreactive T cells (n = 5). Normal donor PBMCs were cocultured with HLA-mismatched DCs, and the expression of surface markers and intracellular cytokines in the proliferating alloreactive T-cell population was determined by gating on the CFSEdim population using FACS analysis. Data shown are means ± SD. (B) CD71 is highly expressed in proliferating CD25 alloreactive T cells (n = 5). CFSE labeled T cells were cocultured with HLA-mismatched DCs, and the kinetics of expression of surface markers and intracellular cytokines in the proliferating alloreactive CD25 population were determined flow cytometrically by gating on the CFSEdimCD25 cells. Results are means ± SD.

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