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. 2022 Sep 27;72(4):917–928. doi: 10.1007/s00262-022-03290-6

Fig. 5.

Fig. 5

dnTGFβRII confers resistance against TGF-β in LCAR-M23 CAR T cells. a Western blotting of SMAD2 and pSMAD2 expression in LCAR-M23 CAR T cells and F3M CAR T cells. Results showed that dnTGFβRII inhibited phosphorylation of SMAD2. b Proliferation of LCAR-M23 CAR T cells and F3M CAR T cells in a long-term co-culture assay. c Tumour growth curve based on data obtained after analysis using the OVCAR-8 xenograft mouse model. LCAR-M23 CAR T cells exhibited more potent antitumour efficacy than F3M CAR at a suboptimal dose. d Distribution of T cells in the tumour of 3 groups determined by IHC staining with anti-human CD45 antibody, anti-human CD4 antibody, anti-human CD8α antibody, anti-human Foxp 3 antibody CAR, chimeric antigen receptor; dnTGFβRII, dominant-negative transforming growth factor-β receptor type II; MSLN, mesothelin; SMAD2, mothers against decapentaplegic homolog 2; pSMAD2, phosphorylated SMAD2, TGF-β1, transforming growth factor beta 1; UnT, untransduced T cells; IHC, immunohistochemistry. n = 3 each group, × 400 magnification, scale bar represents 50 μm. Quantification of CD45, CD8, CD4 and Foxp 3/CD4 score of all groups by the criterion has been described in the methods. Error bars represent mean ± SEM. *p < 0.05 ** p < 0.01, *** p < 0.001