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. 2021 Dec 23;9(12):e002843. doi: 10.1136/jitc-2021-002843

Figure 5.

Figure 5

CD8+ T cells mediated the antitumor immunity of VV-scFv-TIGIT. (A) Treatment scheme of H22 ascites model. (B, C) The depletion of CD8+ T cells and NK cells in the blood (B) or ascites (C) of mice was analyzed by flow cytometry. (D) Representative diagram of flow cytometric analysis of tumor cells and lymphocytes in the ascites. (E) Flow cytometric analysis of the proportion of tumor cells, lymphocytes, and their subpopulations in the ascites. (F) The levels of cytokines in the ascites were detected by ELISA. (G) Kaplan-Meier survival curves of tumor-bearing mice. ns, no significant differences; *p<0.05; **p<0.01; ***p<0.001; ****p<0.0001. PBS, phosphate-buffered saline; scFv, single-chain variable fragment; TIGIT, T-cell immunoglobulin and ITIM domain; VV, vaccinia virus.