The mouse Pdl1 gene and Cd39 gene were replaced by human PD-L1 and CD39 coding sequence in B-hPD-L1/hCD39 MC38 cells. Human PD-L1 and CD39 are highly expressed on the surface of B-hPD-L1/hCD39 MC38 cells.

Gene targeting strategy for B-hPD-L1/hCD39 MC38 cells. The exogenous promoter and human PD-L1 coding sequence was inserted to replace part of murine exon 3. The insertion disrupts the endogenous murine Pdl1 gene, resulting in a non-functional transcript. The exogenous promoter and human CD39 coding sequence were inserted into the targeting vector used in the lentivirus system. 

PD-L1 and CD39 expression analysis in B-hPD-L1/hCD39 MC38 cells by flow cytometry. Single cell suspensions from wild-type MC38 and B-hPD-L1/hCD39 MC38 cultures were stained with species-specific anti-PD-L1 and anti-CD39 antibody. Human PD-L1 and CD39 were detected on the surface of B-hPD-L1/hCD39 MC38 cells but not wild-type MC38 cells. The 3-A09 clone of B-hPD-L1/hCD39 MC38 cells was used for in vivo experiments.

Subcutaneous homograft tumor growth of B-hPD-L1/hCD39 MC38 cells. B-hPD-L1/hCD39 MC38 cells (5x10⁵, 1x10⁶) and wild-type MC38 cells (5x10⁵) were subcutaneously implanted into B-hPD-1/hCD39 mice (female, 8-week-old, n=8). Tumor volume and body weight were measured twice a week. (A) Average tumor volume ± SEM. (B)  Body weight (Mean± SEM). Volume was expressed in mm³ using the formula: V=0.5 X long diameter X short diameter². As shown in panel A, B-hPD-L1/hCD39 MC38 cells were able to establish tumors in vivo and can be used for efficacy studies.

B-hPD-L1/hCD39 MC38 tumor cells growth of individual mice. B-hPD-L1/hCD39 MC38 cells(5x10⁵, 1x10⁶) and wild-type MC38 cells (5x10⁵) were subcutaneously implanted into B-hPD-1/hCD39 mice (female, 8-week-old, n=8). As shown in panel, . B-hPD-L1/hCD39 MC38 cells were able to establish tumors in vivo and can be used for efficacy studies.