Figure 3
Figure 3. The therapeutic effect of combination of ibrutinib plus CpG is T cell dependent. Mice were inoculated with H11 cells and treated with ibrutinib and intratumoral injection of CpG. Tumor outgrowth of (A) SCID mice, (B) nude mice, (C) T-cell depleted wild-type C57BL/6 mice (CD4/CD8) or both T cells were depleted by IP injection of anti-CD4 (GK1.5 clone) or anti-CD8 T cells (2.43 clone). Complete depletion of the CD8 or the CD4 T-cell populations was confirmed by flow cytometry of peripheral blood. Abs were given days 3, 2, 1, and 0 before treatment and the depletion was maintained throughout the experiment. Groups included: isotype control, CD4 T-cell–depleted, CD8 T-cell–depleted, and CD8- and CD4-cell–depleted mice. Each line represents the average left, nontreated tumor measurement of 10 mice. Two separate experiments with similar results were performed. Error bars indicate SD. NS, not significant.

The therapeutic effect of combination of ibrutinib plus CpG is T cell dependent. Mice were inoculated with H11 cells and treated with ibrutinib and intratumoral injection of CpG. Tumor outgrowth of (A) SCID mice, (B) nude mice, (C) T-cell depleted wild-type C57BL/6 mice (CD4/CD8) or both T cells were depleted by IP injection of anti-CD4 (GK1.5 clone) or anti-CD8 T cells (2.43 clone). Complete depletion of the CD8 or the CD4 T-cell populations was confirmed by flow cytometry of peripheral blood. Abs were given days 3, 2, 1, and 0 before treatment and the depletion was maintained throughout the experiment. Groups included: isotype control, CD4 T-cell–depleted, CD8 T-cell–depleted, and CD8- and CD4-cell–depleted mice. Each line represents the average left, nontreated tumor measurement of 10 mice. Two separate experiments with similar results were performed. Error bars indicate SD. NS, not significant.

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