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. 2018 Apr 5;31:66–78. doi: 10.1016/j.ebiom.2018.04.001

Fig. 1.

Fig. 1

Expression and function of chimeric Art v 1-specific TCR and HLA-DR1. A, Flow cytometry analysis of TCR Vβ18 and HLA-DR1 expression on CD4+ and CD45R/B220+ PB lymphocytes isolated from WT, DR1, TCR and TCR-DR1 mice. Markers indicate negative control mAbs, numbers show percentage of cells. n = 4 per group of four analyses. B, Percentages of CD3+CD4+Foxp3+ cells in lymph nodes of WT, DR1, TCR and TCR-DR1 mice. Symbols represent individual mice. C, Dose dependent proliferation of TCR-DR1 splenocytes upon incubation with rArt v 1-protein, or Bet v 1142–153-peptide (negative control). kcpm, kilo counts per minute of incorporated [3H]-thymidine. Shown are representative SEMs of triplicate cultures of one out of four independent experiments. ***p < .001, Kruskal-Wallis test and Mann-Whitney-U test followed by post hoc Bonferroni correction.