Fig. 6.
Fig. 6. Effect of a metalloproteinase inhibitor on IL-18/IL-2 lethality and effect of IL-18/IL-2 in gene knockout mice. / (A) Effect of a metalloproteinase inhibitor on IL-18/IL-2 lethality. Metalloproteinase inhibitor (KB-R7785) was suspended in sterile 0.5% CMC at 10 mg/mL. B6 mice (n = 10 per group) were treated daily with an intraperitoneal injection of 0.2 mL KB-R7785 or 0.5% CMC (vehicle). Then mice were daily treated with IL-18 (1 μg) plus IL-2 (50 000 IU) or control PBS for 10 days. (B) (C) Effect of IL-18/IL-2 in IFN-γ−/− (GKO) (panel B), IL-4−/−, IL-13−/−, IL-4/IL-13−/−, and Stat6−/− mice (panel C). Mice (n = 5 to 20 per group) were treated daily with IL-18 (1 μg) plus IL-2 (50 000 IU) for 21 days.

Effect of a metalloproteinase inhibitor on IL-18/IL-2 lethality and effect of IL-18/IL-2 in gene knockout mice.

(A) Effect of a metalloproteinase inhibitor on IL-18/IL-2 lethality. Metalloproteinase inhibitor (KB-R7785) was suspended in sterile 0.5% CMC at 10 mg/mL. B6 mice (n = 10 per group) were treated daily with an intraperitoneal injection of 0.2 mL KB-R7785 or 0.5% CMC (vehicle). Then mice were daily treated with IL-18 (1 μg) plus IL-2 (50 000 IU) or control PBS for 10 days. (B) (C) Effect of IL-18/IL-2 in IFN-γ−/− (GKO) (panel B), IL-4−/−, IL-13−/−, IL-4/IL-13−/−, and Stat6−/− mice (panel C). Mice (n = 5 to 20 per group) were treated daily with IL-18 (1 μg) plus IL-2 (50 000 IU) for 21 days.

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