Figure 4
Figure 4. Correlation between AnV and CD45RO expression levels. Total tonsillar lymphocytes were stained for GC and naive B-cell subsets as before with the addition of anti-AnV–APC. (A) RO versus AnV contour plots are shown for each population, including the APC-isotype control. The total percentage of AnV+ cells is indicated. *Distribution of AnV+ cells across the RO spectrum (ie, 94.5% of all AnV+ GC B cells [0.6%] are RO− compared with only 0.5% of RO+ GC cells). The proximity of most AnV+ cells to the RO−/RO+/− boundary suggests the RO− fraction can be further subdivided, highlighting an RO−/lo fraction. (B) CD69 MFIs were calculated for AnV− (□) and AnV+ (■) cells within each RO fraction. In the case of RO+ where there was a dearth of AnV+ cells, comparisons were made by gating on the highest and lowest 5% of cells under the AnV bell curve. × denotes no data point.

Correlation between AnV and CD45RO expression levels. Total tonsillar lymphocytes were stained for GC and naive B-cell subsets as before with the addition of anti-AnV–APC. (A) RO versus AnV contour plots are shown for each population, including the APC-isotype control. The total percentage of AnV+ cells is indicated. *Distribution of AnV+ cells across the RO spectrum (ie, 94.5% of all AnV+ GC B cells [0.6%] are RO compared with only 0.5% of RO+ GC cells). The proximity of most AnV+ cells to the RO/RO+/− boundary suggests the RO fraction can be further subdivided, highlighting an RO−/lo fraction. (B) CD69 MFIs were calculated for AnV (□) and AnV+ (■) cells within each RO fraction. In the case of RO+ where there was a dearth of AnV+ cells, comparisons were made by gating on the highest and lowest 5% of cells under the AnV bell curve. × denotes no data point.

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