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. 2026 Jan 21;123(4):e2511733123. doi: 10.1073/pnas.2511733123

Fig. 7.

A multi-part figure shows: A) Experimental design. B) Morphology and weights. C) H and E and I H C. D) Quantification of IHC in pancreata.

Impact of CD4+ and CD8+ T cell depletion on C29h cytotoxicity. (A) Schematic of experimental design and treatments. Orthotopic pancreatic tumors were generated in C57BL/6 N mice and treated with C29h, CD4+ or CD8+ T cell–depleting antibodies, or isotype controls. (B) Gross morphology of tumor-bearing pancreata (Left) and corresponding tumor weights (Right). Each point = one tumor. Mean ± SD (n = 4 to 8 mice per group). One-way ANOVA with Šídák’s multiple comparisons test; *P < 0.05, **P < 0.01, ns-not significant. (C) Representative H&E and IHC for cCasp-3, CD8, and Ki-67 in pancreata from above-treated mice. (Scale bars, 50 µm.) (D) Quantification of IHC in the same pancreata; CD8+ T cell density normalized to tissue area (cells/mm2) and averaged per tumor. Data are shown as mean ± SEM (n = 4 to 8 mice per group). One-way ANOVA with Šídák’s multiple comparisons test; *P < 0.05, **P < 0.01, ***P < 0.001, ****P < 0.0001, ns-not significant.