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. 2023 Jan 27;12:13. doi: 10.1186/s40164-023-00375-5

Fig. 4.

Fig. 4

Cytokine production and proliferation ability of CD26neg/low/high CD8+ T cells in CLL. A Representative flow plots, (B) the frequency of TNF-α, (C) IFN-γ, and (D) TNF-α+IFN-γ+ cells among CD26neg/low/high CCR7CD8+ T cells. E Representative plots, (F) cumulative data showing the frequency of TNF-α+, (G) IFN-γ+, and (H) TNF-α+IFN-γ+ among CD26neg/low/high CCR7CD8+ T cells in unstimulated or stimulated with anti-CD3/CD28 (3 gμ/ml, 1 gμ/ml) and a cocktail of IL-18 + IL-12 + IL-15 (100 ng/ml of each). (I) Representative flow plots and, (J) cumulative data of the frequency of IL-2 expressing cells among CD26neg/low/high CD8+ T cells in unstimulated (black color) versus 5 h after in-vitro stimulation with PMA/ionomycin cocktail (Biolegend, 2 ng/ml) in the presence of Brefeldin A (1 gμ/ml). (K) Representative flow plots and, (L) cumulative data of the frequency of CFSElow (proliferated) cells among CD26neg/low/high CCR7CD8+ T cells, unstimulated (black color) versus 72 h stimulation. (M) Representative flow plots, and (N) cumulative data showing the MFI for ROR γδ in CD26neg, CD26low, and CD26high CD8+ T cells in CLL. Error bars represent the median with an interquartile range. Each dot represents an individual human sample