FIgure 2.
Risk of CMV reactivation based on clinical and laboratory parameters. (A) Major lymphocyte subsets in patients treated with letermovir after allo-HCT: ALC, CD3+CD4+CD8− T cells (CD4), CD3+CD4−CD8+ T-cells (CD8), CD3−CD56+ NK cells, CD3−CD19+ B cells (CD19) are shown. There were no statistically significant differences between patients who experienced or those who did not experience csCMVi. (B) Pre-letermovir discontinuation IgG levels. ∗P < .05; ∗∗P < .005 (Wilcoxon rank-sum test).

Risk of CMV reactivation based on clinical and laboratory parameters. (A) Major lymphocyte subsets in patients treated with letermovir after allo-HCT: ALC, CD3+CD4+CD8 T cells (CD4), CD3+CD4CD8+ T-cells (CD8), CD3CD56+ NK cells, CD3CD19+ B cells (CD19) are shown. There were no statistically significant differences between patients who experienced or those who did not experience csCMVi. (B) Pre-letermovir discontinuation IgG levels. ∗P < .05; ∗∗P < .005 (Wilcoxon rank-sum test).

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