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. Author manuscript; available in PMC: 2021 Oct 1.
Published in final edited form as: J Immunol. 2020 Aug 26;205(7):1867–1877. doi: 10.4049/jimmunol.2000347

FIGURE 5. CD70 but not CD80/CD86 signaling in Batf3 dependent cells plays a critical role in expansion and antitumor efficacy of infused Pmel-1 T cells.

FIGURE 5.

(A) Frequency of infused Pmel-1 T cells (CD8+ CD90.1+) among total CD45+ cells in peripheral blood of B16 tumor-bearing mixed bone marrow chimera mice (Batf3−/− and WT→WT, Batf3−/− and CD70−/−→WT mice, or Batf3−/− and CD80−/−→WT mice) 7 days after ACT ± Vac (hgp100, agonistic anti-CD40 Ab, and TLR7 agonist). (n = 5–7 mice per group). NS, not significant, *P <0.05, ***P <0.001 by one-way ANOVA with Tukey’s multiple comparisons. Mice were irradiated (500 cGy) before ACT.

(B) Survival curves in B16 tumor-bearing mixed bone marrow chimera mice (Batf3−/− and WT→WT, Batf3−/− and CD70−/−→WT mice, Batf3−/− and CD80−/−→WT mice) treated with ACT ± Vac (hgp100, agonistic anti-CD40 Ab, and TLR7 agonist) (n = 6–13 mice per group). Data shown are pooled from two independent experiments. *P < 0.05, ***P < 0.001 using log-rank (Mantel-Cox) test.

Values are mean ± SEM.