Figure 1.
Figure 1. Association of CMV reactivation with T- and NK-cell reconstitution at 100 days in unrelated donor allografts using BM vs PB as a graft source. The frequency of CD4+ T cells (A), CD8+ T cells (B), and total NK cells (C) were determined based on a lymphocyte gate determined by forward and side scatter. The NK cells (CD56+/CD56− gate) were subsetted into CD56bright (D), CD56dim (E), and KIR+NKG2A− (F) NK cells in 3 groups based on CMV reactivation status and in BM vs PB groups separately. Blue numbers on the x-axis show medians. CMVr, patients who reactivated CMV by day 100; CMV+, CMV-seropositive patients who did not reactivate CMV by day 100; and CMV−, CMV-seronegative patients who did not reactivate CMV by day 100. *P < .05; **P < .01; ***P < .001.

Association of CMV reactivation with T- and NK-cell reconstitution at 100 days in unrelated donor allografts using BM vs PB as a graft source. The frequency of CD4+ T cells (A), CD8+ T cells (B), and total NK cells (C) were determined based on a lymphocyte gate determined by forward and side scatter. The NK cells (CD56+/CD56 gate) were subsetted into CD56bright (D), CD56dim (E), and KIR+NKG2A (F) NK cells in 3 groups based on CMV reactivation status and in BM vs PB groups separately. Blue numbers on the x-axis show medians. CMVr, patients who reactivated CMV by day 100; CMV+, CMV-seropositive patients who did not reactivate CMV by day 100; and CMV−, CMV-seronegative patients who did not reactivate CMV by day 100. *P < .05; **P < .01; ***P < .001.

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