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. 2021 May 11;13(10):2295. doi: 10.3390/cancers13102295

Figure 6.

Figure 6

Therapy-treated OB-RES mice have a sustained CD8+ TIL effector response that is blunted in DIO mice. (A) CD44+CD8+ TILs at day 17–18, day 21, and day 27–28 post-tumor challenge across groups. (B) Linear regression of CCL5 concentrations versus CD44+CD8+ TILs at day 21 post-tumor challenge. (C) The frequencies of CD11bCD11c+I-Ad+ TDLN DCs and (D) CD86 expression on TDLN CD11bCD11c+I-Ad+ DCs; (E) the frequencies of TDLN CD44+CD8+ T cells and (F) the proliferative capacity (Ki-67+) in TDLN CD44+CD8+ T cells at days 17–18 post-tumor challenge. (G) Cell viability and death markers at day 21 post-tumor challenge in CD44+CD8+ TILs. (H) Intracellular expression of IFNγ and (I) the mean fluorescent intensity of IFNγ in ex vivo stimulated CD44+CD8+ TILs at day 21 post-tumor challenge. (J) IFNγ+CD44+CD8+ TILs as a percent of single cells at day 21 post-tumor challenge. Data from n = 2–5 independent experiments. Fold change value calculated using no therapy control for each group. # denotes non-parametric test. # p < 0.05, ## p < 0.01, ### p < 0.001, #### p < 0.0001. ns: non-significant, NT: no therapy, TX: AdT/CpG+αCTLA-4.