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. 2024 May 20;22:207. doi: 10.1186/s12916-024-03420-0

Fig. 1.

Fig. 1

Antitumor activity and homing ability of TILs in PDX model. A PDX models were established in B-NDG mice from a local cervical cancer recurrence patient which were randomly divided into two groups: group control, which received cryoprotectant, and group TIL, which received homologous TILs generated from the same patient. Tumor volume was measured three times per week, using vernier calipers and calculated using formula A×B2× 0.5, where A and B represented the longest and shortest diameters of the tumor, respectively. Tumor volumes in group TIL were smaller than in group control (p < 0.0001). B The peripheral blood of PDX mice was obtained on day 40 post infusion for flow cytometry. C The tumor samples of PDX mice were obtained on day 40 post infusion for multiplexed immunohistochemistry (mIHC), using the following markers: Ki67, panCK, CD8, and DAPI. The scale bar is 100 µm. PDX, patient-derived xenografts