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. Author manuscript; available in PMC: 2019 Feb 6.
Published in final edited form as: J Autoimmun. 2016 Jul 5;73:100–110. doi: 10.1016/j.jaut.2016.06.015

Fig. 1. MOG35–55-primed, but not OVA323–339-primed, Th cells accumulate in the meninges and CNS early in EAE.

Fig. 1.

Four x106 MOG35–55- or OVA323–339-primed T cell blasts from Thy1.1+ donor mice were restimulated with peptide in vitro and transferred to congenic Thy1.2+ recipients. The frequency and numbers of Thy1.1+CD45+CD4+ cells in the meninges (a,c) and CNS (b,c) was determined 3 or 6 days post transfer. (a) Representative analysis of MOG35–55 or OVA323–339-primed CD4+Thy1.1+ T cells detected in the pooled meninges of Thy1.2+ recipients at day 6 post transfer. (b) Representative analysis of MOG35–55 or OVA323–339-primed CD4+Thy1.1+ T cells detected in the CNS (pooled brain and spinal cord) of Thy1.2+ recipients 6 days post transfer. Percentages of the CD45+/hi parent gate are shown. (c) Numbers of CD45+CD4+Thy1.1+ MOG35–55 or OVA323–339-primed T cells in the meninges and CNS at indicated days post T cell transfer. For meninges samples, each point represents the analysis of a pool of tissues from 3 to 5 mice and is expressed as numbers/mouse. CNS data points represent the analysis of individual mice. *p < 0.05 and **p < 0.01 by Student’s t-Test. 4 independent experiments.