Fig. 2.
Fig. 2. Preservation of allogeneic GVL effects in IL-12–treated mice. Results from three individual experiments are shown in each column. B10 (H-2b) mice were lethally irradiated on day 0. (A through C) Nonleukemic mice received 5 × 106 TCD B10 BMC and 15 to 18 × 106 B10 spleen cells with or without IL-12 treatment (Syn BMT +/− IL-12), or 5 × 106 TCD B10 BMC plus 10 × 106 A/J BMC and 15 to 18 × 106 A/J spleen cells with (Allo BMT + IL-12) or without (Allo BMT) IL-12 treatment. (D through F ) Leukemic recipients in the same experiments received 5 × 106 TCD B10 BMC and 15 to 18 × 106 B10 spleen cells alone with (Syn BMT + EL4 + IL-12) or without (Syn BMT + EL4) IL-12 treatment, or 5 × 106 TCD BMC plus 10 × 106 A/J BMC and 15 to 18 × 106 A/J spleen cells with (Allo BMT + EL4 + IL-12) or without (Allo BMT + EL4) IL-12 treatment. All leukemic recipients received 500 H-2b EL4 cells on the day of BMT.

Preservation of allogeneic GVL effects in IL-12–treated mice. Results from three individual experiments are shown in each column. B10 (H-2b) mice were lethally irradiated on day 0. (A through C) Nonleukemic mice received 5 × 106 TCD B10 BMC and 15 to 18 × 106 B10 spleen cells with or without IL-12 treatment (Syn BMT +/− IL-12), or 5 × 106 TCD B10 BMC plus 10 × 106 A/J BMC and 15 to 18 × 106 A/J spleen cells with (Allo BMT + IL-12) or without (Allo BMT) IL-12 treatment. (D through F ) Leukemic recipients in the same experiments received 5 × 106 TCD B10 BMC and 15 to 18 × 106 B10 spleen cells alone with (Syn BMT + EL4 + IL-12) or without (Syn BMT + EL4) IL-12 treatment, or 5 × 106 TCD BMC plus 10 × 106 A/J BMC and 15 to 18 × 106 A/J spleen cells with (Allo BMT + EL4 + IL-12) or without (Allo BMT + EL4) IL-12 treatment. All leukemic recipients received 500 H-2b EL4 cells on the day of BMT.

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