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. 2017 May 8;7:1519. doi: 10.1038/s41598-017-01771-8

Figure 2.

Figure 2

LM-PLP infection protects mice from EAE in a CD8-dependent antigen-specific manner. (A) B6 mice were infected with LM-PLP or LM-OVA on d-7 and immunized with PLP178-191/CFA on d0 and monitored for clinical disease. (B) B6 mice were infected with LM-PLP or LM-OVA, followed by induction of EAE with non-cognate antigen MOG35-55/CFA. Disease scores are shown. (C) CD8-KO mice were infected with either LM-PLP or LM-OVA on d-7, immunized with PLP178-191/CFA on d0 and monitored for clinical disease. (D) CD8 T cells harvested from LM-PLP or LM-OVA-infected B6 mice were stimulated in vitro with PLP178-191 and OVA257-264 respectively, and adoptively transferred into naïve recipients followed by subsequent immunization with PLP178-191/CFA and the monitoring of clinical disease. (E) Perf-KO mice were infected with LM-PLP or LM-OVA on d-7, immunized with PLP178-191/CFA on d0, and monitored for clinical disease. (F) IFN-γ-KO mice were infected with LM-PLP or LM-OVA on d-7, immunized with PLP178-191/CFA on d0, and monitored for clinical disease as depicted. (G) Inflammation and (H) Spheroid/axon dilation scores from H&E stained lumbar spinal cord sections from infected and immunized mice on d18 post-immunization. Data are representative of at least two independent experiments in each panel. *p < 0.05, **p < 0.01, ***p < 0.001 ****p < 0.0001.