Figure 7
Figure 7. GVT effect is maintained after ECP treatment. (A) Specific killing of target (T) tumor cell lines A20 (left) and Bcl1 (right) by effector CD8+ T cells (E) is shown. CD8+ T cells were isolated from ECP-treated (ECP) or nontreated (Tcon) mice 10 days after BMT and were added to 51Cr-labeled target cells at an E:T ratio of 20:1 and 5:1. Specific killing occurred in both target cells, but with reduced efficiency in ECP-treated mice. (B) GVT effects in vivo are maintained in ECP-treated mice in a Bcl1 tumor model. Recipients were injected with 5 × 103 luc+Bcl1 cells 9 days prior to BMT. Tumor-bearing recipients were transplanted with Tcon alone (blue, ▲), or additionally received ECP-treated splenocytes from healthy mice (red, ▼) 48 hours prior to BMT. Results are done in triplicates and are representative of 2 individual experiments (A) or are compiled from 2 experiments with 10 mice per group (B).

GVT effect is maintained after ECP treatment. (A) Specific killing of target (T) tumor cell lines A20 (left) and Bcl1 (right) by effector CD8+ T cells (E) is shown. CD8+ T cells were isolated from ECP-treated (ECP) or nontreated (Tcon) mice 10 days after BMT and were added to 51Cr-labeled target cells at an E:T ratio of 20:1 and 5:1. Specific killing occurred in both target cells, but with reduced efficiency in ECP-treated mice. (B) GVT effects in vivo are maintained in ECP-treated mice in a Bcl1 tumor model. Recipients were injected with 5 × 103luc+Bcl1 cells 9 days prior to BMT. Tumor-bearing recipients were transplanted with Tcon alone (blue, ▲), or additionally received ECP-treated splenocytes from healthy mice (red, ▼) 48 hours prior to BMT. Results are done in triplicates and are representative of 2 individual experiments (A) or are compiled from 2 experiments with 10 mice per group (B).

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