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. 2018 May 15;2(10):1101–1114. doi: 10.1182/bloodadvances.2017015404

Figure 5.

Figure 5.

Absence of the CD57/NKG2C NK cell phenotype otherwise found in HCMV-EBV coinfection. NK cell subsets, including CD56brightCD16neg (1), CD56brightCD16pos (2), CD56dimCD16pos (3), and CD56negCD16pos (4), were evaluated for each group of children: Nandi (EBVlow/malarialow), Kisumu (EBVhigh/malariahigh), and eBL patients with no/low EBV and high EBV loads. (A) Comparison of CD57 among the different NK cell subsets across study groups. (B) CD57 expression on the CD56negCD16pos NK cell subset across study groups. (C) Comparison of NKG2C expression among different NK cell subsets across groups of children. (D) NKG2C expression on the CD56negCD16pos NK cell subset across study groups. (E) Median fluorescence intensity (MFI) of antibody titers against CMV. (F) Coexpression of CD57 and NKG2C on CD56dimCD16pos and CD56negCD16pos NK cells. (G) CD57posNKG2Cpos expression between CD56dimCD16pos and CD56negCD16pos subsets across study groups. For CD57, Nandi, n = 8; Kisumu, n = 6, and BL, n = 11. For NKG2C, Nandi, n = 7; Kisumu, n = 5; and BL, n = 11. Data are mean ± SD. *P < .05, **P < .01, ***P < .001.