Figure 3.
Malignant B cells are in frequent contact with PD-1+ T cells. (A) Representative high-power mIF image demonstrating PD-1 expression on the surface of CD3+ T cells in contact with a PAX5+ B cells). (B) Cell-cell contact map of the mIF image shown in panel A (same scale). PD-1+ T cells, PD-1− T cells, and other cells (solid gray) in contact with malignant cells and PD-1+ T cells and PD-1− T cells (outlined) not in contact with malignant cells. (C) Proportion of malignant cell contacts for individual cases (●) displayed according to the proportion of PD-1+ T-cell contacts vs PD-1− T-cell contacts (n = 26). (D) Low-power, maximum field-of-view mIF image of TCRLBCL in panel A: PD-1 on CD3+ T cells intermixed with PAX5+ B cells. (E) Cell phenotype map corresponding to the mIF image in panel D: PD-1+ T cells, PD-1− T cells, and malignant B cells. (F) T-cell density for individual cases (●) displayed according to the density of PD-1+ T cells and PD-1− T cells. (G) Intermediate-power mIF image of the boxed region in panel D: PD-1 expression on CD3+ T cells intermixed with PAX5+ B cells. (H) Cell proximity map of the region highlighted in panel E: spatial distribution of PD-1+ T cells and PD-1− T cells relative to malignant cells, showing T cells that are located <75 μm from malignant cells and those that are located ≥75 μm from malignant cells. (I) The ratio of PD-1+ T cells to total T cells for individual cases (●) displayed according whether the T cells are located <75 or ≥75 μm from malignant B cells. For the box-and-whisker plots (C,F,I), the median (line), 25th and 75th percentiles (boxes), and extreme values (whiskers) are indicated. Statistical comparisons by the 2-sided Mann-Whitney U test, Wilcoxon matched-pairs signed-rank test, and the Kruskal-Wallis test with Dunn’s test for multiple comparisons.

Malignant B cells are in frequent contact with PD-1+ T cells. (A) Representative high-power mIF image demonstrating PD-1 expression on the surface of CD3+ T cells in contact with a PAX5+ B cells). (B) Cell-cell contact map of the mIF image shown in panel A (same scale). PD-1+ T cells, PD-1 T cells, and other cells (solid gray) in contact with malignant cells and PD-1+ T cells and PD-1 T cells (outlined) not in contact with malignant cells. (C) Proportion of malignant cell contacts for individual cases (●) displayed according to the proportion of PD-1+ T-cell contacts vs PD-1 T-cell contacts (n = 26). (D) Low-power, maximum field-of-view mIF image of TCRLBCL in panel A: PD-1 on CD3+ T cells intermixed with PAX5+ B cells. (E) Cell phenotype map corresponding to the mIF image in panel D: PD-1+ T cells, PD-1 T cells, and malignant B cells. (F) T-cell density for individual cases (●) displayed according to the density of PD-1+ T cells and PD-1 T cells. (G) Intermediate-power mIF image of the boxed region in panel D: PD-1 expression on CD3+ T cells intermixed with PAX5+ B cells. (H) Cell proximity map of the region highlighted in panel E: spatial distribution of PD-1+ T cells and PD-1 T cells relative to malignant cells, showing T cells that are located <75 μm from malignant cells and those that are located ≥75 μm from malignant cells. (I) The ratio of PD-1+ T cells to total T cells for individual cases (●) displayed according whether the T cells are located <75 or ≥75 μm from malignant B cells. For the box-and-whisker plots (C,F,I), the median (line), 25th and 75th percentiles (boxes), and extreme values (whiskers) are indicated. Statistical comparisons by the 2-sided Mann-Whitney U test, Wilcoxon matched-pairs signed-rank test, and the Kruskal-Wallis test with Dunn’s test for multiple comparisons.

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