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. Author manuscript; available in PMC: 2022 Jan 26.
Published in final edited form as: Nat Immunol. 2021 Jul 26;22(8):1030–1041. doi: 10.1038/s41590-021-00982-6

Figure 4: Functional analysis reveals that TESC, but not TEX after viral cure, display functional properties similar to those of TMEM from HCV natural resolvers.

Figure 4:

a, Representative flow cytometry plots of the cytokine production and cytotoxicity capability of HCV-specific CD8+ T cells following ex vivo stimulation with or without cognate antigen. The co-expression patterns and percentage of cells producing IFNγ, TNFα and IL-2 cytokines and expressing CD107a are indicated. b, Dot plot histograms displaying IFNγ, TNFα and IL-2 production as well as CD107a expression across TEX (paired samples, n=8) and TESC (paired samples, n=7) pre- and post-DAA therapy, and in resolver TMEM (n=8). Triangles identify two analyzed TP-ESC populations. Statistical testing by Mann-Whitney tests when comparing TEX versus TF-ESC or TMEM (unpaired, nonparametric, two-sided), or by Wilcoxon tests (paired, nonparametric, two-sided) when comparing paired samples pre- versus post-DAA. A schematic representation of the comparison rules and statistical tests used are presented in Extended Data Fig. 3c. c, Overlapping pie-charts describing the polyfunctionality of TEX (paired samples, n=8) and TESC (paired samples, n=7) pre- and post-DAA therapy, as well as TMEM (n=8), after ex vivo stimulation with cognate antigens. d, Frequencies of T cells with one, two and three or more functions as defined by the expression or co-expression of CD107a, IFNγ, TNFα and IL-2 after stimulation with cognate antigens. Statistical testing by Mann-Whitney tests (unpaired, nonparametric, two-sided). b,d, *P < 0.05, **P < 0.01, ***P < 0.001.