Wnt inhibition reactivates immune responses in IDH1WT GBM allografts. (a) Representative [18F]DPA714-PET/CT images of mouse brains bearing IDH1WT GBM allografts at 7 and 14 days after treatment with the Wnt/β-catenin inhibitor Wnt-C59 (15 mg/kg). Right panel, intratumoral SUVmean at 30 min post [18F]DPA714 injection at 14 days (n = 4). Flow cytometric analysis of immunostimulatory (CD16/32+) and immunosuppressive (CD206+ CD16/32+) subtypes among CD11b+ CD45+ Iba1+ CD49d− microglia (b), CD8+ T cells and CD4+ T cells among CD45+ CD3+ cells (c), and CD4+ FOXP3+ T cells among CD45+ CD25+ CD8− cells (d) in untreated and Wnt-C59 (7.5 or 15 mg/kg)-treated model mice (n = 4). (e) Immunoblots showing CD163, Wnt3a, GSK-3β and β-catenin protein expression in tumor tissues isolated from untreated and treated model mice. (f) mRNA expression of IFN-γ, iNOS, TGF-β and IL-10 in the above samples (n = 3). In panel a, values are shown as Mean±SEM. In panel b, c, d and f, values are shown as Mean±SD. Student’s t-test. *p < .05; **p < .01 and ***p < .001