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Updated: Jun 18, 2026

Visualizing Impairment of the Endothelial and Glial Barriers of the Neurovascular Unit during Experimental Autoimmune Encephalomyelitis In Vivo
Published on: March 26, 2019
Mild experimental autoimmune encephalitis as a tool to induce blood-brain barrier dysfunction
Michael K Boettger1, Andreas Weishaupt, Christian Geis
1Department of Neurology, University of Würzburg, Josef-Schneider-Strasse 11, 97080 Würzburg, Germany. michael.boettger@mti.uni-jena.de
The blood-brain barrier (BBB) becomes permeable during experimental autoimmune encephalomyelitis (EAE), allowing large molecules like immunoglobulins to enter the central nervous system. This model aids in studying autoimmune CNS disorders.
Area of Science:
- Neuroscience
- Immunology
- Pathology
Background:
- The blood-brain barrier (BBB) restricts immunoglobulin entry into the central nervous system (CNS).
- BBB integrity is crucial in antibody-mediated autoimmune CNS disorders.
Purpose of the Study:
- To characterize BBB dysfunction in a mild experimental adoptive transfer autoimmune encephalomyelitis (AT-EAE) model.
- To assess the permeability of the BBB to large molecules during AT-EAE.
Main Methods:
- Induction of mild experimental adoptive transfer autoimmune encephalomyelitis (AT-EAE) in a suitable animal model.
- Monitoring and characterization of blood-brain barrier permeability over time post-induction.
Main Results:
- Significant BBB dysfunction was observed between days 3 and 7 after EAE induction.
- Large molecules, including immunoglobulins, were found to readily penetrate the BBB during this period.
Conclusions:
- The characterized AT-EAE model exhibits transient BBB breakdown.
- This model is suitable for investigating the role of immunoglobulins in the pathogenesis of autoimmune CNS diseases.
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