Figure 4
Figure 4. siRNA4+ EBV-CTLs retain their immunophenotype, cytotoxic activity, and EBV-antigen specificity. (A) The immunophenotype of NT and irr-siRNA+ EBV-CTLs and of siRNA4+ EBV-CTLs cultured in the presence of FK506. Means ± SD are shown for the 6 CTL lines. No significant phenotypic differences were observed for siRNA4+ CTLs expanded in the presence of FK506. (B) The results of a standard 51Cr release assay of NT and irr-siRNA+ EBV-CTLs and of irr-siRNA+ and siRNA4+ EBV-CTLs cultured in the presence of FK506. Targets were K562, autologous LCLs, and allogeneic LCLs. Shown is the CTL/tumor cell ratio of 20:1. Bars represent the mean ± SD of the EBV-CTLs generated from 6 donors. No significant differences in cytotoxic activity were observed for siRNA4+ CTLs versus NT or irr-siRNA+ CTLs. (C) The frequencies of multimers recognizing latent EBV-associated antigens (EBNA3B-AVF and EBNA3B-IVT) in NT (left plots) and irr-siRNA+ (middle plots) EBV-CTLs and in siRNA4+ (right plots) EBV-CTLs cultured in the presence of FK506 for 3 weeks in 1 representative donor. (D) The frequency of CTLs responding to the indicated EBV-specific peptides assessed by IFNγ ELIspot assay in another representative donor.

siRNA4+ EBV-CTLs retain their immunophenotype, cytotoxic activity, and EBV-antigen specificity. (A) The immunophenotype of NT and irr-siRNA+ EBV-CTLs and of siRNA4+ EBV-CTLs cultured in the presence of FK506. Means ± SD are shown for the 6 CTL lines. No significant phenotypic differences were observed for siRNA4+ CTLs expanded in the presence of FK506. (B) The results of a standard 51Cr release assay of NT and irr-siRNA+ EBV-CTLs and of irr-siRNA+ and siRNA4+ EBV-CTLs cultured in the presence of FK506. Targets were K562, autologous LCLs, and allogeneic LCLs. Shown is the CTL/tumor cell ratio of 20:1. Bars represent the mean ± SD of the EBV-CTLs generated from 6 donors. No significant differences in cytotoxic activity were observed for siRNA4+ CTLs versus NT or irr-siRNA+ CTLs. (C) The frequencies of multimers recognizing latent EBV-associated antigens (EBNA3B-AVF and EBNA3B-IVT) in NT (left plots) and irr-siRNA+ (middle plots) EBV-CTLs and in siRNA4+ (right plots) EBV-CTLs cultured in the presence of FK506 for 3 weeks in 1 representative donor. (D) The frequency of CTLs responding to the indicated EBV-specific peptides assessed by IFNγ ELIspot assay in another representative donor.

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