Developmental control of CD8+ T cell–avidity maturation in autoimmune diabetes
J. Clin. Invest. Bingye Han, et al. 115:1879 doi:10.1172/JCI24219 [
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Figure 2Developmental biology of 17.6α/8.3β versus 17.4α/8.3β TCRs in Tg mice. Flow cytometry of thymocytes (
A–
D) and splenocytes (
E–
H). (
A and
E) Representative CD4 versus CD8 dot plots.
P values for thymic and splenic CD4:CD8 ratios were
P < 0.0001 (for 17.4α/8.3β TCR-Tg vs. non-Tg mice) and
P < 0.03 (for 17.6α/8.3β TCR-Tg vs. non-Tg mice). (
B–
D and
F–
H) Comparison of the intensity with which the different T cell subsets stain with anti–TCR-Vβ8 or anti–TCR-β mAbs or with IGRP
206–214 tetramers. Values on the panels correspond to percentage of cells contained within each quadrant (
A and
E) or to percentage of cells within each gate that stained (
B–
D and
F–
H; only values for the 2 Tg strains are shown in these panels for ease of comparison) (mean ± SE). **
P < 0.05 vs. 17.4α/8.3β Tg mice. Representative histograms are shown.
A–
D and
E–
H represent 3–6 mice per strain.