Figure 6.
Figure 6. Enhancement of CD30-specific CTL cytotoxicity in XIAP down-regulated H-RS cells. Specificity of target cell lysis mediated by CD30-specific T cells. Isolated peripheral blood CD3+ T cells grafted by retroviral gene transfer with the CD30-specific HRS3scFv-Fc-zeta immunoreceptor and nontransduced T cells were incubated with CD30- Colo320 (A) or CD30+ L540 (B) cells (each 5 × 105 cells/well) for 24 hours. Viability of target cells was monitored by an XTT-based colorimetric assay. XIAP down-regulation improves antigen-specific CTL cytotoxicity against HL cells. Nontransduced and HRS3scFv-Fc-zeta receptor-grafted CD3+ T cells were incubated for 24 hours with L540-scr-shRNA or L540-XIAP-shRNA target cells (each 5 × 105 cells/well). Viability of target cells was monitored by an XTT-based colorimetric assay. Data are mean ± SD values from 3 individual experiments performed in triplicate.

Enhancement of CD30-specific CTL cytotoxicity in XIAP down-regulated H-RS cells. Specificity of target cell lysis mediated by CD30-specific T cells. Isolated peripheral blood CD3+ T cells grafted by retroviral gene transfer with the CD30-specific HRS3scFv-Fc-zeta immunoreceptor and nontransduced T cells were incubated with CD30- Colo320 (A) or CD30+ L540 (B) cells (each 5 × 105 cells/well) for 24 hours. Viability of target cells was monitored by an XTT-based colorimetric assay. XIAP down-regulation improves antigen-specific CTL cytotoxicity against HL cells. Nontransduced and HRS3scFv-Fc-zeta receptor-grafted CD3+ T cells were incubated for 24 hours with L540-scr-shRNA or L540-XIAP-shRNA target cells (each 5 × 105 cells/well). Viability of target cells was monitored by an XTT-based colorimetric assay. Data are mean ± SD values from 3 individual experiments performed in triplicate.

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