Figure 1.
Figure 1. Induction of autologous CLL-specific CTL responses by DCs transfected with whole-tumor RNA. Immature DCs generated from the peripheral blood of 2 patients with CLL (A, patient no. 1; B, patient no. 2) were electroporated with 10 μg whole-tumor RNA isolated from autologous malignant B cells. After further incubation with 10 ng/mL TNF-α for 24 hours DCs were used as APCs for in vitro CTL induction. Cytolytic activity of the CTLs was determined on day 5 after the last restimulation by using autologous purified leukemic cells or nonmalignant B lymphocytes as targets in a standard 51Cr-release assay. Blocking of HLA class I molecules with the monoclonal antibody W06/32 was performed to analyze the HLA class I restriction of the elicited CTL responses. K562 tumor cells were included to determine the NK cell activity. A cold target inhibition assay was performed to further assess the specificity of the CTLs induced with the DCs from patient no. 1 (C). The lysis of autologous CLL cells (pulsed with 51Cr, hot targets) could be blocked by addition of unpulsed autologous CLL cells (cold targets) but not by nonmalignant autologous peripheral blood mononuclear cells (PBMNCs).

Induction of autologous CLL-specific CTL responses by DCs transfected with whole-tumor RNA. Immature DCs generated from the peripheral blood of 2 patients with CLL (A, patient no. 1; B, patient no. 2) were electroporated with 10 μg whole-tumor RNA isolated from autologous malignant B cells. After further incubation with 10 ng/mL TNF-α for 24 hours DCs were used as APCs for in vitro CTL induction. Cytolytic activity of the CTLs was determined on day 5 after the last restimulation by using autologous purified leukemic cells or nonmalignant B lymphocytes as targets in a standard 51Cr-release assay. Blocking of HLA class I molecules with the monoclonal antibody W06/32 was performed to analyze the HLA class I restriction of the elicited CTL responses. K562 tumor cells were included to determine the NK cell activity. A cold target inhibition assay was performed to further assess the specificity of the CTLs induced with the DCs from patient no. 1 (C). The lysis of autologous CLL cells (pulsed with 51Cr, hot targets) could be blocked by addition of unpulsed autologous CLL cells (cold targets) but not by nonmalignant autologous peripheral blood mononuclear cells (PBMNCs).

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