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. Author manuscript; available in PMC: 2011 Jan 1.
Published in final edited form as: Clin Cancer Res. 2010 May 14;16(13):3409–3419. doi: 10.1158/1078-0432.CCR-10-0644

Figure 1. Ifnar1−/− mice exhibit accelerated tumor growth and death following SB-based induction of gliomas.

Figure 1

(A) CNS gliomas were induced in C57BL/6-background Ifnar1−/− (red lines) or WT (black lines) neonatal mice by intraventricular transfection of the following plasmids: pT2/C-Luc//PGK-SB1.a3 (0.2 μg), pT/CAG-NRas (0.4 μg), and pT/shp53 (0.4 μg). Tumor growth (left) and symptom-free survival (right) were monitored. P-values are based on log-rank test. (B) Glioma cells derived from Ifnar1−/− (solid lines) or WT (dashed lines) mice were injected into the basal ganglia of Ifnar1−/− (red lines) or WT (black lines) host mice (1 × 105/mouse). Tumor growth (left) and symptom-free survival (right) were monitored. (C) 51Cr release assay was performed to evaluate cytolytic ability of cervical LN cells obtained from the mice bearing Ifnar1−/− cells (solid lines in B) against the Ifnar1−/− and WT cell lines. (D) ELISA was performed to evaluate the amount of mIFN-γ secretion by the CTLs used in (C) per the last 24 hrs. (C and D) I: Ifnar1−/−; W: WT. Lines within boxes denote means; box upper and lower bounds indicate SD; whiskers indicate minimum and maximum values. P-values are based on Holm’s post hoc test.