Figure 2
Figure 2. Accumulation and terminal differentiation of the CD56dim NKG2A+ KIR− NK-cell subset during acute IM. PBMCs from controls and IM patients were analyzed by flow cytometry. (A) Frequencies of CD56dim NKG2A+ KIR− NK cells within the CD56dim population from representative healthy control, IM-acute, 1-month, and 6-month patients. Frequencies of (B) CD56dim NKG2A+ KIR− and (C) CD56dim NKG2A− KIR+ NK cells in healthy EBV-negative controls (n = 17), healthy EBV-positive controls (n = 20), IM-like patients (n = 12), and IM-acute (n = 17), 1-month (n = 11), 6-month (n = 10), and 2-year (n = 4) patients. Frequencies of CD57+ cells within (D) the CD56dim NKG2A+ KIR− and (E) the CD56dim NKG2A− KIR+ NK-cell subsets in healthy EBV-negative controls (n = 17), healthy EBV-positive controls (n = 20), and IM-acute (n = 17), 1-month (n = 11), 6-month (n = 10), and 2-year (n = 4) patients. Horizontal lines or single symbols indicate median values. Error bars indicate interquartile ranges. Mann-Whitney U tests.

Accumulation and terminal differentiation of the CD56dim NKG2A+ KIR NK-cell subset during acute IM. PBMCs from controls and IM patients were analyzed by flow cytometry. (A) Frequencies of CD56dim NKG2A+ KIR NK cells within the CD56dim population from representative healthy control, IM-acute, 1-month, and 6-month patients. Frequencies of (B) CD56dim NKG2A+ KIR and (C) CD56dim NKG2A KIR+ NK cells in healthy EBV-negative controls (n = 17), healthy EBV-positive controls (n = 20), IM-like patients (n = 12), and IM-acute (n = 17), 1-month (n = 11), 6-month (n = 10), and 2-year (n = 4) patients. Frequencies of CD57+ cells within (D) the CD56dim NKG2A+ KIR and (E) the CD56dim NKG2A KIR+ NK-cell subsets in healthy EBV-negative controls (n = 17), healthy EBV-positive controls (n = 20), and IM-acute (n = 17), 1-month (n = 11), 6-month (n = 10), and 2-year (n = 4) patients. Horizontal lines or single symbols indicate median values. Error bars indicate interquartile ranges. Mann-Whitney U tests.

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