Figure 3.
Figure 3. Peripheral-blood IgD+ CD38hi T1 B cells are not circulating pre–germinal-center or plasma-cell precursors. (A) Tonsil mononuclear cells were stained with anti-CD19, anti-IgD, anti-CD38, and a fourth mAb to examine the phenotype of IgD+ CD38hi pre–germinal center B cells. (B) Enriched B cells from peripheral blood of a healthy donor were similarly stained to examine the expression of plasma cell markers on CD19+ IgD+ CD38hi T1 B cells (solid gate) and CD19lo IgD- CD38bright circulating plasma cells (dashed gate). (C) The relative frequencies of the CD19+ IgD+ CD38hi T1 B-cell population (solid gate) and CD19lo IgD- CD38bright plasma cells (dashed gate) from a healthy donor were examined before immunization and 4, 7, and 14 days after immunization with influenza vaccine.

Peripheral-blood IgD+ CD38hi T1 B cells are not circulating pre–germinal-center or plasma-cell precursors. (A) Tonsil mononuclear cells were stained with anti-CD19, anti-IgD, anti-CD38, and a fourth mAb to examine the phenotype of IgD+ CD38hi pre–germinal center B cells. (B) Enriched B cells from peripheral blood of a healthy donor were similarly stained to examine the expression of plasma cell markers on CD19+ IgD+ CD38hi T1 B cells (solid gate) and CD19lo IgD- CD38bright circulating plasma cells (dashed gate). (C) The relative frequencies of the CD19+ IgD+ CD38hi T1 B-cell population (solid gate) and CD19lo IgD- CD38bright plasma cells (dashed gate) from a healthy donor were examined before immunization and 4, 7, and 14 days after immunization with influenza vaccine.

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