Figure 2
Figure 2. Differentiation phenotype and IL-7 responsiveness of human tk+ mH antigen-specific CTLs. (A) The differentiation phenotype of tk+ mH antigen-specific CTLs after either 2 rounds (mH×2) or 4 rounds (mH×4) of antigenic stimulation was evaluated by flow cytometry and is expressed as the percentage of CD45RA−/CCR7− (left panel), of CD28−/CD27+ (middle panel), and of IL-15Rβ+/IL-7Rα+ cells (right panel). Each symbol represents the result from a single donor of a group of n = 2 HLA-A2pos/HA-1neg and n = 3 HLA-A2pos/H-Yneg donors. Results from a t test paired statistical analysis are shown (*P < .05). (B) The percentage of either mH×2 or mH×4 tk+ mH antigen-specific CTLs binding annexin V after culture in the absence of antigen and in the presence (■) or in the absence (□) of exogenous IL-7 was evaluated by flow cytometry. Means ± SD of the data from n = 2 HLA-A2pos/HA-1neg and n = 2 HLA-A2pos/H-Yneg donors and results from a paired t test statistical analysis are shown (*P < .05, **P < .01). (C) The expansion of mHx2 tk+ mH antigen-specific CTLs after multiple, weekly rounds of stimulation with PHA (x-axis) is expressed as fold growth (y-axis). (D) The percentage of IL-7Rα+ cells (y-axis) was evaluated by flow cytometry before each round of PHA stimulation (x-axis). Results from linear regression analysis are shown (exact P values).

Differentiation phenotype and IL-7 responsiveness of human tk+ mH antigen-specific CTLs. (A) The differentiation phenotype of tk+ mH antigen-specific CTLs after either 2 rounds (mH×2) or 4 rounds (mH×4) of antigenic stimulation was evaluated by flow cytometry and is expressed as the percentage of CD45RA/CCR7 (left panel), of CD28/CD27+ (middle panel), and of IL-15Rβ+/IL-7Rα+ cells (right panel). Each symbol represents the result from a single donor of a group of n = 2 HLA-A2pos/HA-1neg and n = 3 HLA-A2pos/H-Yneg donors. Results from a t test paired statistical analysis are shown (*P < .05). (B) The percentage of either mH×2 or mH×4 tk+ mH antigen-specific CTLs binding annexin V after culture in the absence of antigen and in the presence (■) or in the absence (□) of exogenous IL-7 was evaluated by flow cytometry. Means ± SD of the data from n = 2 HLA-A2pos/HA-1neg and n = 2 HLA-A2pos/H-Yneg donors and results from a paired t test statistical analysis are shown (*P < .05, **P < .01). (C) The expansion of mHx2tk+ mH antigen-specific CTLs after multiple, weekly rounds of stimulation with PHA (x-axis) is expressed as fold growth (y-axis). (D) The percentage of IL-7Rα+ cells (y-axis) was evaluated by flow cytometry before each round of PHA stimulation (x-axis). Results from linear regression analysis are shown (exact P values).

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