Extended Data Fig. 9: CD44s-hiCD49dlo CD8+ T cells exhibit activation in a TCR-independent manner and enhanced proliferation capacity compared to other cell populations.

a-c, Following cytokine stimulation, various cells from SDLNs were incubated for 48 h and flow cytometric analysis performed (50 ng/ml IL-2, 50 ng/ml IL-7, 50 ng/ml IL-12, 50 ng/ml IL-15, or 50 ng/ml IL-18). a, The percentage of GzmB+ and perforin+ cells in AA and naïve TVM cells, respectively (n = 16, AA TVM; n = 17, naïve TVM). b, The percentage of IFNγ+ cells (n = 11, AA TVM; n = 8, naïve TVM) and TNF+ cells in AA TVM cells and naive TVM cells (n = 11, AA TVM; n = 12, naïve TVM). c, Comparison of the percentage of GzmB+ cells, perforin+ cells, IFNγ+ cells, and TNF+ cells among each cell population in the presence of IL-15 (n = 12, naïve; n = 11, AA) or IL-12/18 (n = 8, naïve TVM IFNγ+; n = 12, naïve TVM TNF+; n = 11, AA). d, e, Following cytokine stimulation, various cells from SDLNs were incubated for 96 h. Representative flow cytometry plot of CTVlow cells (d) and the percentage of CTVlow cells in AA TVM cells (n = 7) and naïve TVM cells (n = 4) (e). f, gMFI of NKG2D in each cell population (n = 4, AA TVM; n = 4, naïve TVM). g, Comparison of the gMFI of NKG2D among each cell population without stimulation or in the presence of IL-15 (n = 4 per group). Data were acquired from AtAA mice. Data are presented as mean values ± SD. A Mann-Whitney test was performed for comparisons between two groups. All tests were two sided. ****P < 0.0001.