Figure 1.
T-cell compartment in recipients without aGVHD after HCT. Shown are results for donor/recipient couples without aGVHD from cohort 1. (A) Frequency of CD3+ T cells within the lymphocyte population (left panel) and frequencies of CD4+ (middle panel) and CD8+ (right panel) T cells within CD3+ T cells. (B) Ratio of CD4+/CD8+ T cells in recipients (R) at day 90 post-HCT compared with their respective sibling donors (D). (C) Gating strategy used to identify naive and memory subsets within the CD4+ and CD8+ T-cell compartments in donors and recipients after transplantation by polychromatic flow cytometry. (D) Frequencies of TNaive, TSCM-like, TCM, TEM, and TEMRA cells within the CD4+ (upper panels) and CD8+ (lower panels) T-cell compartments in recipients (R) at day 90 post-HCT compared with their respective sibling donors (D). (E) Frequency of proliferating Ki-67+ cells in total CD4+ and CD8+ T cells and in the different naive and memory subsets in CD4+ (left panel) and CD8+ (right panel) compartments in donors and recipients. The frequency of Ki-67+ cells is represented as the percentage of Ki-67–expressing cells within total CD4+ or CD8+ T cells and as the percentage Ki-67–expressing cells within the parent gate for TNaive, TCM, TEM, and TEMRA cell subsets. Horizontal lines indicate the median. P values were calculated using the Wilcoxon matched-pairs Student t test (donor vs respective recipient). Differences are considered significant for P < .05.

T-cell compartment in recipients without aGVHD after HCT. Shown are results for donor/recipient couples without aGVHD from cohort 1. (A) Frequency of CD3+ T cells within the lymphocyte population (left panel) and frequencies of CD4+ (middle panel) and CD8+ (right panel) T cells within CD3+ T cells. (B) Ratio of CD4+/CD8+ T cells in recipients (R) at day 90 post-HCT compared with their respective sibling donors (D). (C) Gating strategy used to identify naive and memory subsets within the CD4+ and CD8+ T-cell compartments in donors and recipients after transplantation by polychromatic flow cytometry. (D) Frequencies of TNaive, TSCM-like, TCM, TEM, and TEMRA cells within the CD4+ (upper panels) and CD8+ (lower panels) T-cell compartments in recipients (R) at day 90 post-HCT compared with their respective sibling donors (D). (E) Frequency of proliferating Ki-67+ cells in total CD4+ and CD8+ T cells and in the different naive and memory subsets in CD4+ (left panel) and CD8+ (right panel) compartments in donors and recipients. The frequency of Ki-67+ cells is represented as the percentage of Ki-67–expressing cells within total CD4+ or CD8+ T cells and as the percentage Ki-67–expressing cells within the parent gate for TNaive, TCM, TEM, and TEMRA cell subsets. Horizontal lines indicate the median. P values were calculated using the Wilcoxon matched-pairs Student t test (donor vs respective recipient). Differences are considered significant for P < .05.

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