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Updated: Aug 12, 2026

Induction and Clinical Scoring of Chronic-Relapsing Experimental Autoimmune Encephalomyelitis
Published on: July 4, 2007
Reinduction of experimental autoimmune encephalomyelitis in mice
J W Lindsey1, M Pappolla, L Steinman
1Department of Neurology, University of Texas-Houston Health Science Center 77030, USA.
Abstract:
Experimental autoimmune encephalomyelitis (EAE) in Lewis rats and some strains of mice is typically a monophasic disease, and recovered animals are resistant to reinduction of disease. We demonstrate that SJL mice remain susceptible to disease after recovery, and suffer a second episode of disease when reinjected with spinal cord homogenate in complete Freund's adjuvant. Reinduced disease occurs earlier after injection than the initial disease (mean onset 7.3 days compared with 14.5 days), and has comparable severity and incidence. The susceptibility to reinduced disease is present for at least 20 weeks after the initial injection. If the initial episode of EAE is elicited using a synthetic peptide of proteolipid protein, then reinjection of the same peptide causes reinduced disease. PL/J mice and PL/J x SJL F1 mice are also susceptible to reinduced disease which occurs with an accelerated onset and higher incidence than the initial disease. We conclude that SJL and PL/J mice have a defect in immunoregulation which causes them to be susceptible to recurrent episodes of autoimmune disease.
Insights
SJL mice are susceptible to recurrent experimental autoimmune encephalomyelitis (EAE), experiencing a faster onset of a second disease episode after recovery. This suggests an immunoregulation defect in these mice, unlike other strains resistant to EAE reinduction.
Area of Science:
- Neuroimmunology
- Autoimmune Diseases
Background:
- Experimental autoimmune encephalomyelitis (EAE) is typically monophasic in most mouse strains.
- Recovered animals usually develop resistance to subsequent EAE induction.
Purpose of the Study:
- To investigate the susceptibility of SJL mice to reinduced EAE.
- To characterize the kinetics and features of recurrent EAE in susceptible mouse models.
Main Methods:
- Induction of EAE in SJL mice using spinal cord homogenate.
- Reinduction of EAE after initial recovery via reinjection of antigen.
- Assessment of disease onset, severity, and incidence.
Main Results:
- SJL mice remained susceptible to reinduced EAE, with earlier onset (7.3 days vs. 14.5 days) and comparable severity/incidence.
- Susceptibility to reinduced EAE persisted for at least 20 weeks.
- PL/J and PL/J x SJL F1 mice also showed accelerated onset and higher incidence of reinduced EAE.
Conclusions:
- SJL and PL/J mice possess a defect in immunoregulation.
- This defect renders them susceptible to recurrent episodes of autoimmune central nervous system disease.
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