Fig. 4: apCAFs modulated immune profile and promoted antitumor immune response. | Nature Communications

Fig. 4: apCAFs modulated immune profile and promoted antitumor immune response.

From: Antigen-presenting cancer associated fibroblasts enhance antitumor immunity and predict immunotherapy response

Fig. 4: apCAFs modulated immune profile and promoted antitumor immune response.

A Schematic representation of apCAFs adoptive transfer in vivo experiments. Created in BioRender. Song, J. (2024) https://BioRender.com/j06i038. B Tumor growth curves showing tumor volume in mice from control group, apCAFs group and MHC II- CAFs group (n = 5 mice/per group). Error bars represent the mean ± SD. Statistical significance was determined using one-way ANOVA, followed by a two-sided Dunnett’s test to compare the specific differences between the groups. Source data are provided as a Source Data file. C Distribution of immune cell clusters in tumors from control, apCAFs and MHC II- CAFs groups (n = 2 mice/per group). D The proportion immune cell clusters in tumors from control, apCAFs and MHC II- CAFs groups (n = 2 mice/per group). E Relative proportion of total CD4+ T, CD69+CD4+ T cells, IFN-γ+CD4+ T cells and GZMB+CD4+ T cells in tumors from control, apCAFs and MHC II- CAFs groups (n = 5 mice/per group). Error bars represent the mean ± SEM. Statistical significance was determined using one-way ANOVA, followed by a two-sided Dunnett’s test to compare the specific differences between the groups. Source data are provided as a Source Data file. F Relative proportion of total CD8+ T, GZMB+CD8+ T cells, IFN-γ+CD8+ T cells and TNF+CD8+ T cells in tumors from control, apCAFs and MHC II- CAFs groups (n = 5 mice/per group). Error bars represent the mean ± SEM. Statistical significance was determined using one-way ANOVA, followed by a two-sided Dunnett’s test to compare the specific differences between the groups. Source data are provided as a Source Data file. G The concentration of IFN-γ within tumors from control, apCAFs and MHC II- CAFs groups (n = 5 mice/per group). The box is bounded by the first and third quartile with a horizontal line at the median and whiskers extend to the maximum and minimum value. Statistical significance was determined using one-way ANOVA, followed by a two-sided Dunnett’s test to compare the specific differences between the groups. Source data are provided as a Source Data file. H The concentration of TNF within tumors from control, apCAFs and MHC II- CAFs groups (n = 5 mice/per group). The box is bounded by the first and third quartile with a horizontal line at the median and whiskers extend to the maximum and minimum value. Statistical significance was determined using one-way ANOVA, followed by a two-sided Dunnett’s test to compare the specific differences between the groups. Source data are provided as a Source Data file. I Representative images of multiplex immunofluorescence showing T cell marker (green: CD3) and cytotoxic molecule (red: GZMB) expression in the high apCAFs group (n = 80) and low apCAFs group (n = 60) from the FUSCC cohort. J Relative proportion of overall T cells (CD3+ cells) and cytotoxic T cells (GZMB+CD3+ cells) in high apCAFs group (n = 70) and low apCAFs group (n = 70) in FUSCC cohort. Error bars represent the mean ± SEM. Statistical significance was determined using Mann–Whitney two-sided test. Source data are provided as a Source Data file.

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