Fig. 1: NKG2A+ cells are enriched in CD103+ CD39+ (DP) CD8 T cells in HNSCC tumors. | Nature Communications

Fig. 1: NKG2A+ cells are enriched in CD103+ CD39+ (DP) CD8 T cells in HNSCC tumors.

From: IL-12 drives the expression of the inhibitory receptor NKG2A on human tumor-reactive CD8 T cells

Fig. 1

a Flow cytometry analysis and (b) summary of NKG2A expression by CD8 T cells from the blood and the tumor of HNSCC patients (n = 25). c Unsupervised clustering of blood (red) and tumor-infiltrating (cyan) CD3+ CD8+ T cells isolated from 13 HNSCC patients. d Normalized expression of CD103, CD39 and NKG2A on CD8 T cells from blood and tumor. e NKG2A expression on blood and tumor CD8 T cells (positive cells are shown as red dots), with B1 and B2 representing subsets of NKG2A+ cells in the blood, and T1, T2 and T3 representing subsets of NKG2A+ cells in the tumor. f Phenotype of the different subsets of NKG2A+ CD8 T cells (n = 13). g Frequency of DN (CD39 CD103 ), SP (CD39 CD103+ ) and DP (CD39+ CD103+ ) cells among NKG2A (left) and NKG2A+ (right) CD8 TILs in HNSCC patients (n = 25). h Summary of the expression of NKG2A by DP CD8 TILs in HPV (n = 23) and HPV+ (n = 18) HNSCC patients. Horizontal lines indicate the mean ± SEM. NS= not significant; p-values were determined by paired 2-tailed t test (b), by one-way analysis of variance with Tukey’s post hoc testing (g), or unpaired 2-tailed t test (h).

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