Figure 1.
Figure 1. Defective grzB/CTL-mediated cytotoxicity in HL cells. (A) PBMCs from healthy volunteer donors were activated at a density of 5 × 106 cells/mL by ConA (2 μg/mL) in complete RPMI medium for 5 days. Redirected CTL activity was assayed by coincubating for 4 hours 51Cr-labeled target cells at graded effector-target ratios with activated PBMCs in the presence of ConA (5 μg/mL). Thereafter, the activity of 51Cr was measured in the cell-free supernatants using a gamma counter. Jurkat T-cell as well as L1309 B-cell lines were used as positive controls for CTL-mediated target cells lysis. (B) Control L1309 B cells and Jurkat T cells (□) or L428 and L540 HL cells () (all 106) were treated with adenovirus at an moi of 100 with or without 600 ng/mL isolated human grzB and incubated for 4 hours at 37°C. Data are mean ± SD values from 3 different individual experiments performed in triplicate.

Defective grzB/CTL-mediated cytotoxicity in HL cells. (A) PBMCs from healthy volunteer donors were activated at a density of 5 × 106 cells/mL by ConA (2 μg/mL) in complete RPMI medium for 5 days. Redirected CTL activity was assayed by coincubating for 4 hours 51Cr-labeled target cells at graded effector-target ratios with activated PBMCs in the presence of ConA (5 μg/mL). Thereafter, the activity of 51Cr was measured in the cell-free supernatants using a gamma counter. Jurkat T-cell as well as L1309 B-cell lines were used as positive controls for CTL-mediated target cells lysis. (B) Control L1309 B cells and Jurkat T cells (□) or L428 and L540 HL cells () (all 106) were treated with adenovirus at an moi of 100 with or without 600 ng/mL isolated human grzB and incubated for 4 hours at 37°C. Data are mean ± SD values from 3 different individual experiments performed in triplicate.

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