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Determining Immune System Suppression versus CNS Protection for Pharmacological Interventions in Autoimmune Demyelination
Published on: September 12, 2016
Suppression of autoimmunity via microbial mimics of altered peptide ligands
L Steinman1, P J Utz, W H Robinson
1Dept of Neurological Sciences and Interdepartmental Program in Immunology, Beckman Center for Molecular Medicine B002, Stanford University School of Medicine, CA 94305, USA. steinman@stanford.edu
Abstract:
Molecular mimics of self-antigens can behave as altered peptide ligands and serve to ameliorate autoimmune disease. Analysis of experimental autoimmune encephalomyelitis with proteomic autoantibody microarrays reveals that there might exist a wide variety of microbes with features that mimic self-epitopes. Autoimmunity could therefore be modulated via microbial immunity, which may account for relapse and remission of ongoing disease.
Insights
Molecular mimics, like altered peptide ligands, can treat autoimmune diseases. Microbial immunity may explain disease relapses and remissions by mimicking self-epitopes.
Area of Science:
- Immunology
- Microbiology
- Autoimmune Diseases
Background:
- Autoimmune diseases involve the immune system attacking the body's own tissues.
- Altered peptide ligands (molecular mimics) show potential in treating autoimmune conditions.
- The role of microbial factors in autoimmune disease pathogenesis is increasingly recognized.
Purpose of the Study:
- To investigate the potential of molecular mimics in ameliorating autoimmune disease.
- To explore the link between microbial antigens and self-epitopes in autoimmunity.
- To understand how microbial immunity influences the course of autoimmune diseases like experimental autoimmune encephalomyelitis.
Main Methods:
- Utilized proteomic autoantibody microarrays for comprehensive analysis.
- Studied experimental autoimmune encephalomyelitis (EAE) as a model for autoimmune disease.
- Analyzed microbial features that mimic self-epitopes.
Main Results:
- Identified a diverse range of microbes possessing features that mimic self-epitopes.
- Demonstrated that molecular mimics can act as altered peptide ligands.
- Provided evidence for microbial modulation of autoimmune responses.
Conclusions:
- Molecular mimics of self-antigens offer a therapeutic strategy for autoimmune diseases.
- Microbial mimicry of self-epitopes is a significant factor in autoimmune disease.
- Microbial immunity plays a crucial role in the cyclical nature (relapse and remission) of autoimmune conditions.
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