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. Author manuscript; available in PMC: 2015 Jun 15.
Published in final edited form as: J Immunol. 2014 May 2;192(12):5561–5570. doi: 10.4049/jimmunol.1400385

Figure 2. The abnormal T cell distribution in CVID-Mgat2ΔM/ΔM mice is maintained with age and independent of changes in T cell surface glycosylation.

Figure 2

A) Representative analysis of blood CD4+ T cell phenotype from the same naïve Mgat2ΔM/ΔM or CVID-Mgat2ΔM/ΔM mouse at 12 and 27 weeks of age. Comparison between B) T cell (CD3+) and C) neutrophil (Gr1+CD11b+) cell glycosylation profiles from Mgat2wt/wt, naïve Mgat2ΔM/ΔM, and CVID-Mgat2ΔM/ΔM mice using flow cytometry and fluorescently labeled PHA-L lectin. *p<0.05