Figure 6
Figure 6. Changes in βGL1-22– and LGL1-reactive T cells in a murine model of GD. (A) Bar graphs summarizing the percentage of CD1d-βGL1-22/LGL1 tetrameter-positive T cells in spleen and lymph node (LN) of GBA−/− mice. (B) Comparison of frequency of CD1d-βGL1-22, LGL1, and α-GalCer tetrameter-positive T cells between WT C57BL/6 (WT) and GBA1-deficient (GBA−/−) mice splenocytes. Data are presented as mean ± SEM from 3 different mice. (C) Compiled results comparing the percentage of CXCR5hi PD-1hi tetrameter-positive T cells between WT and GBA−/− mice. Data are presented as mean ± SEM from 3 different mice. *P < .01.

Changes in βGL1-22– and LGL1-reactive T cells in a murine model of GD. (A) Bar graphs summarizing the percentage of CD1d-βGL1-22/LGL1 tetrameter-positive T cells in spleen and lymph node (LN) of GBA−/− mice. (B) Comparison of frequency of CD1d-βGL1-22, LGL1, and α-GalCer tetrameter-positive T cells between WT C57BL/6 (WT) and GBA1-deficient (GBA−/−) mice splenocytes. Data are presented as mean ± SEM from 3 different mice. (C) Compiled results comparing the percentage of CXCR5hi PD-1hi tetrameter-positive T cells between WT and GBA−/− mice. Data are presented as mean ± SEM from 3 different mice. *P < .01.

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