Figure 2.
CMV reactivation differentially affects CD56, NKG2C, and NKG2A NK cell expression among patients receiving TCD, T-replete, and DUCB HCT. Data gathered at late time points after different allograft infusions are shown. (A) CD56bright (top) and CD56dim (bottom) population frequencies within CD56+ NK cells in patients stratified based on the CMV reactivation status. (B) CD56dim (left), CD56bright (middle), and CD56– (right) population frequencies within total NK cells in patients stratified according to CMV reactivation status. (C) NKG2A+ frequencies within CD56bright (left), CD56dim (middle), and CD56– (right) NK cell subpopulations in patients, stratified based on the CMV reactivation status. (D) NKG2C+ frequencies within CD56bright (left), CD56dim (middle), and CD56neg (right) NK cell subpopulations in patients, stratified based on the CMV reactivation status. (E) NKG2C+ frequencies in total NK cells including CD56bright, CD56dim, and CD56– NK cells, from patients experiencing CMV reactivation. A threshold of 10%, separating individuals with or without expansion, was determined based on patients without CMV reactivation. Unpaired t tests were used for statistical analysis, with ∗P ≤ .05; ∗∗P ≤ .01; ∗∗∗P ≤ .001; ∗∗∗∗P ≤ .0001.

CMV reactivation differentially affects CD56, NKG2C, and NKG2A NK cell expression among patients receiving TCD, T-replete, and DUCB HCT. Data gathered at late time points after different allograft infusions are shown. (A) CD56bright (top) and CD56dim (bottom) population frequencies within CD56+ NK cells in patients stratified based on the CMV reactivation status. (B) CD56dim (left), CD56bright (middle), and CD56 (right) population frequencies within total NK cells in patients stratified according to CMV reactivation status. (C) NKG2A+ frequencies within CD56bright (left), CD56dim (middle), and CD56 (right) NK cell subpopulations in patients, stratified based on the CMV reactivation status. (D) NKG2C+ frequencies within CD56bright (left), CD56dim (middle), and CD56neg (right) NK cell subpopulations in patients, stratified based on the CMV reactivation status. (E) NKG2C+ frequencies in total NK cells including CD56bright, CD56dim, and CD56 NK cells, from patients experiencing CMV reactivation. A threshold of 10%, separating individuals with or without expansion, was determined based on patients without CMV reactivation. Unpaired t tests were used for statistical analysis, with ∗P ≤ .05; ∗∗P ≤ .01; ∗∗∗P ≤ .001; ∗∗∗∗P ≤ .0001.

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