Extended Data Fig. 9: An inflammatory cellular polarization of T cells can be found in liver biopsies from patients with NAFLD or NASH.
From: NASH limits anti-tumour surveillance in immunotherapy-treated HCC

a, b, Flow cytometry plots and quantification of patient-liver-derived PD1+CD8+ T cells (a), and correlation of PD1+CD8+ T cells with BMI, NAS and ALT for healthy participants and patients with NAFLD or NASH (b) (Supplementary Table 1; healthy controls n = 8; NAFLD/NASH n = 16 patients). c–e, Flow cytometry plot of FMO control (c), quantification of patient-liver-derived PD1+CD8+ T cells (d), and quantification of CD4, CD8, γδ, NK and NK T cells from healthy participants or patients with NAFLD or NASH (e) (Supplementary Table 1: healthy controls n = 8; NAFLD/NASH n = 16 patients). f, g, Heat map showing median marker expression (f) and quantification of the defined CD45+ subsets from Fig. 3c (g) by flow cytometry derived from hepatic biopsies from control participants and patients with NAFLD or NASH to define distinct marker expression (Supplementary Table 2: control individuals n = 6; NAFLD/NASH n = 11 patients). h–j, HSNE representation of defined T cell subsets (h), marker expression (i) and quantification of CD8+CD103+PD1+ cells (j) in liver-derived T cells from control individuals and patients with NAFLD or NASH analysed by cytometry by time of flight (CyTOF) (control n = 11 individuals pooled in 3 analyses; NAFLD/NASH n = 16 patients pooled in 5 analyses). k, l, Selected average marker expression in CD4+ and CD8+ T cell subsets (k) and differential gene expression of CD8+PD1+ versus CD8+ T cells and CD4+PD1+ versus CD4+ T cells by scRNA-seq (l) for control individuals and patients with NAFLD or NASH (control n = 4 individuals; NAFLD/NASH n = 7 patients). All data are shown as mean ± s.e.m. All data were analysed by two-tailed Mann–Whitney test.