SKAP55‐deficient mice enhance DC‐based vaccine for prevention of tumors in vivo AWT and SKAP55 KO C57BL/6 mice were s.c. immunized on day −14 and day −7.

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SKAP55‐deficient mice enhance DC‐based vaccine for prevention of tumors in vivo AWT and SKAP55 KO C57BL/6 mice were s.c. immunized on day −14 and day −7 by DCs that were prepulsed with B16F10 tumor lysates. SKAP55‐deficient mice enhance DC‐based vaccine for prevention of tumors in vivo AWT and SKAP55 KO C57BL/6 mice were s.c. immunized on day −14 and day −7 by DCs that were prepulsed with B16F10 tumor lysates. On day 0, the immunized mice were i.v. inoculated with B16F10 cells. Number of lung tumors were counted 26 days after B16F10 challenge (n ≥ 5 mice).B, CAt day 0 (B, before tumor injection) or at day 26 (C, after tumor injection), surface PD‐1 expression in CD44hiCD8+ or CD44hiCD4+ T cells, and the percentages of CD44hiCD8+ T cells or Foxp3+CD4+ cells were analyzed (mean ± SD, n ≥ 5 mice).D, EThe mRNA levels of PD‐1, NFATc1, or the mRNA and protein levels of granzyme B in lung infiltrating CD8+ T cells were examined at day 26 (mean of triplicates ± SD, and the mRNA samples were prepared from at least 3 mice per group).FCTLA‐4 levels in the lung‐infiltrated CD44hiCD8+ T cells or the percentages of CD4+Foxp3+ T cells in lungs, MLN, and spleen were measured at day 26 (mean ± SD, n ≥ 5 mice).Data information: Statistical significance was determined with Mann–Whitney U‐test. Data are representative of three independent experiments. Chunyang Li et al. EMBO Mol Med. 2015;7:754-769 © as stated in the article, figure or figure legend