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. 2016 Nov 17;7:13453. doi: 10.1038/ncomms13453

Figure 5. HCC-derived FcγRIIlow/− B cells suppressed cytotoxic T-cell function via IL-10 signals.

Figure 5

(a) Detection of CD8 (green) and CD20 (red) (n=6) in peritumoral stroma by immunofluorescence. Scale bar, 100 μm. (b) Associations of tumour FcγRIIlow/− B cells with granzyme B+, perforin+, TNF-α+ and IFN-γ+ CD8 T cells (n=20). (c) Expression of IL-10R on CD8+ T cells from paired blood and HCC tumour were determined by FACS (n=6). (d,e) HCC tumour-derived CD8+ T cells were left untreated or cultured with sorted tumour FcγRIIlow/− B cells in the presence or absence of an anti-IL10R or a control Ab. FACS analysis of TNF-α, IFN-γ expression in CD8+ T cells is shown. Results represent three independent experiments (n=5). *P<0.05, **P<0.01 (Student's t-test). Error bars, s.e.m.