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. Author manuscript; available in PMC: 2023 Apr 28.
Published in final edited form as: Sci Immunol. 2022 Oct 21;7(76):eabo0981. doi: 10.1126/sciimmunol.abo0981

Figure 7: Cd4-Cre+ Zfp36l1fl/fl Zfp36l2fl/fl mice are protected from EAE.

Figure 7:

A, Clinical EAE scoring in the indicated strains of mice. B, CD44 and MOG38-49-I-Ab Tetramer staining on CD4+ T cells from the CNS of naïve or MOG35-55 peptide immunized (day 14) Cd4-Cre Zfp36l1fl/fl Zfp36l2fl/fl and Cd4-Cre+ Zfp36l1fl/fl Zfp36l2fl/fl mice. C, Quantitation of CD4+ cells, CD44+ MOG38-49-I-Ab Tetramer+ CD4+ T cells, the frequency of CD44+ MOG38-49-I-Ab Tetramer+ CD4+ T cells, and the frequency of CD44+ MOG38-49-I-Ab Tetramer CD4+ T cells in the CNS of naïve (pooled from 2 experiments, n=4/group) or immunized (day 14) Cd4-Cre Zfp36l1fl/fl Zfp36l2fl/fl and Cd4-Cre+ Zfp36l1fl/fl Zfp36l2fl/fl mice (pooled from 2 experiments, n=6/group). Data in A,C are mean ± s.e.m. Mann-Whitney U test between area under the curve for individual mice (A); two-way ANOVA with Šídák’s multiple comparisons test (C). *P < 0.05; **P < 0.01; ***P < 0.001; ****P < 0.001; ns, not significant.