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. 2021 Jan 21;29(5):1794–1807. doi: 10.1016/j.ymthe.2021.01.021

Figure 6.

Figure 6

CD39+ HBVs-CAR-T cells and CD39+ PTL-HBVs-CAR-T cells exerted potent antitumor activity in the PDX model

(A and B) HCC organoids at 5 × 106 cells were inoculated s.c. into NSG mice. Fifteen days later, various CAR-T cells were infused via tail injection, and GP120-CAR-T cells (NC-CAR-T cells) served as NC. All of the tumors were measured every 5 days (n = 5). (C–E) At day 40, tumors were resected from the mice, followed by digestion and FACS analysis. The percentage of infiltrating CAR-T cells in tumor (C and D) and the percentages of IFN-γ+ cells in tumor-infiltrating CAR-T cells (E) were shown among different groups. ∗p < 0.05, ∗∗p < 0.005, ∗∗∗p < 0.0005 (1-way ANOVA). All data are means ± SEMs.