Table 1.

Induction of redirected antileukemic T-cell cytotoxicity following stimulation with B7-1 immunoglobulin G-coated acute myeloid leukemia-M5 blasts in autologous mixed-lymphocyte tumor culture

Plastic-bound OKT3 (ng per well)Specific lysis from AML-M5 blasts by remission T cells (%) stimulated with AML-M5 blasts according to pretreatment of blasts
CD8 IgGB7-1(CD80) IgGP value*
7.8  ±  3.1 5.0  ±  0.5 —  
23.7  ±  1.0 26.3  ±  1.8 0.05  
26.0  ±  0.2 30.0  ±  3.6 0.05 
24.4  ±  1.6 28.5  ±  2.0 0.05 
Plastic-bound OKT3 (ng per well)Specific lysis from AML-M5 blasts by remission T cells (%) stimulated with AML-M5 blasts according to pretreatment of blasts
CD8 IgGB7-1(CD80) IgGP value*
7.8  ±  3.1 5.0  ±  0.5 —  
23.7  ±  1.0 26.3  ±  1.8 0.05  
26.0  ±  0.2 30.0  ±  3.6 0.05 
24.4  ±  1.6 28.5  ±  2.0 0.05 

Remission PHA blasts, 5 × 104 per well (activated for 3 days), of patient no. 39 with AML-M5a were stimulated with submitogenic concentrations of plastic-bound OKT3 as indicated, and with autologous mitomycin C-inactivated AML blasts (105per well) precoated with saturating concentrations of CD8 IgG and B7-1 IgG on day 0 and 7. Fusion cytokine binding was verified as stated in legend to Figure 3. On day 14 of mixed-lymphocyte tumor culture, cytotoxicity of responding T cells against autologous AML-M5 blasts (5 × 103 per well) in the presence of soluble OKT3 (80 ng/mL) was measured by standard 51Cr-release assay. Mean and SD of triplicate measurements are shown. Spontaneous51Cr-release was 18.2%.

AML indicates acute myloid leukemia; IgG, immunoglobulin G; PHA, phytohemagglutinin; 51Cr, 51chromium.

*

CD8 IgG-pretreated versus B7-1 IgG-pretreated stimulator cells compared by Wilcoxon test for unpaired rank sums.

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