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. Author manuscript; available in PMC: 2017 Mar 1.
Published in final edited form as: J Immunol. 2016 Jan 29;196(5):2401ā€“2409. doi: 10.4049/jimmunol.1502470

Fig. 3.

Fig. 3

Increased frequency of Tfh in the LN post-PBio therapy. (A) Representative staining demonstrating the Tfh population in the LN pre-PBio (left panel) and post-PBio (right panel). Cells were identified by first gating on lymphocytes and excluding doublets using FSC and SSC properties and removing dead cells with an Aqua Live/Dead viability dye. The frequency of Tfh cells within this subset was then determined by gating on CD3+CD4+PD-1hiCXCR5+ cells. (B) Percentage of Tfh in the LN at all time points. Each animal is represented by a different symbol (n=5). Each experiment was performed once per animal per time-point. Statistical significance between the two post-PBio time-points (d28 or d77/80) and the pre-PBio time-point (dāˆ’7) was calculated using a paired t test.