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. 2020 Oct 12;130(11):5800–5816. doi: 10.1172/JCI137265

Figure 5. Kinetics of innate immune cell subsets during H1N1 infection.

Figure 5

(A) Relative abundances of total (first and third panels) and activated (CD38+Ki67+, second and fourth panels) populations of CD56+CD16 NK cells and CD56loCD16+ NK cells. (B) Relative abundances of pDCs, CD1c+ myeloid DCs (mDCs), and BDCA3+ mDCs. (C) Relative abundances of classical monocytes (cMCs; CD14+CD16), intermediate monocytes (intMCs; CD14+CD16+), and nonclassical monocytes (ncMCs; CD14CD16+). (D) Relative abundances of CD66+ cells and CD123+HLA-DR cells. (E and F) Biaxial plots of CD38 and Ki67 expression on CD56loCD16+ NK cells (E) and CD14 and CD16 expression on monocytes (F) on days 1–8 and 29. Plots for 1 representative virus shedder are shown. In BE, values plotted are relative abundance (percentage of CD66 cells normalized to baseline [average of day –1, 1]) (mean ± SEM); data for virus shedders are indicated by filled squares and solid lines, and data for nonshedders are indicated with open squares and dashed lines. (AF) n = 35 volunteers. Bonferroni’s adjusted P value of the time-shedding interaction term. For plots of additional gated cell populations, see Supplemental Figure 6.