Changing tumor immune microenvironment by FUVAC infection
(A) Schedule of the immune microenvironment characterization after MDRVV or FUVAC treatment. Bilateral CT26-bearing mice were treated with MDRVV or FUVAC using the same method as Figure 4. 5 days after the first virus injection (1 day after the third injection), the virus-treated or -untreated tumors were recovered and processed for flow cytometry analysis. (B) The ratio of CD45+ total immune cells and total tumor cells, and the ratio of CD3+ T lymphocyte in CD45+ cells. (C) The ratios of CD3+/CD8+ and CD3+/CD4+ cells in CD45+ T lymphocyte, and the ratio of Treg in CD3+ T cell as determined by the expression levels of CD4, CD25, and FoxP3. (D) The ratio of TAM (CD11b+ F4/80+), M-MDSC (CD11b+ Ly6C+), or G-MDSC (CD11b+ Ly6C– Ly6G+) in CD45+ cells. Data in (B)–(D) are presented as the means ± SEM (n = 7). ∗p < 0.05, ∗∗p < 0.01, ∗∗∗p < 0.001 (two-tailed unpaired t test).