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. Author manuscript; available in PMC: 2017 Apr 15.
Published in final edited form as: Cancer Res. 2016 Feb 15;76(8):2125–2136. doi: 10.1158/0008-5472.CAN-15-1490

Figure 6. Ibrutinib reduces MDSC frequency in vivo.

Figure 6

Eight mice were included in the ibrutinib treatment group and ten mice in the vehicle control group. (A) Splenocytes and single cell suspensions of the tumors were stained with GR-1 and CD11b antibodies. Values are the mean ± SE of GR-1+/CD11b+ MDSC in the spleen and tumor, *p< 0.05. (B) Tumor volumes were measured three times weekly. Values are the mean ± SE of tumor volumes at each time point. (C) Wild type C57BL/6 mice were inoculated with 1×105 B16F10 melanoma cells subcutaneously. After two weeks of treatment mice were sacrificed and the frequency of GR-1+/CD11b+ MDSC in spleen was measured by flow cytometry. Values represented are means ± SE of MDSC from 5 mice for each treatment group, p< 0.05. (D) BTK mutant C57BL/6 XID mice were inoculated with 1×105 B16F10 melanoma cells subcutaneously. After two weeks of treatment mice were sacrificed and the frequency of GR-1+/CD11b+ MDSC in spleen was measured by flow cytometry. Values represented are means ± SE of MDSC from 5 mice for each treatment group, p = 0.73.