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Experimental Autoimmune Encephalomyelitis: A Disease Model to Decode the Complex Interactions between the Nervous and Immune Systems

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Alessandro Didonna

Alessandro Didonna

East Carolina University, Brody School of Medicine, Department of Anatomy and Cell Biology

The main objective of Dr. Didonna’s research activity consists in elucidating the molecular mechanisms underlying central nervous system (CNS) autoimmunity, with an emphasis on disease progression and neurodegenerative phenotypes. For this purpose, he has been extensively using in vivo models of neuroinflammation in combination with advanced mouse genetics and omics technologies. Dr. Didonna earned his PhD degree in Functional and Structural Genomics at the International School for Advanced Studies (SISSA) in Italy, studying the effects of prion replication on neuronal signaling under the mentorship of Dr. Giuseppe Legname. He subsequently joined the lab of Dr. Puneet Opal at Northwestern University, to complete his first postdoctoral fellowship on the molecular basis of spinocerebellar ataxia type 1 (SCA1). In 2013, he pursued a second postdoctoral training in the lab directed by Dr. Jorge Oksenberg at University of California San Francisco (UCSF), focusing on the functional characterization of genetic determinants underpinning multiple sclerosis (MS) susceptibility. After transitioning to a faculty position still at UCSF, Dr. Didonna further expanded his research efforts to the analysis of the events underlying MS progression. In 2021, Dr. Didonna started his own laboratory in the Department of Anatomy and Cell Biology of Brody School of Medicine at East Carolina University.  

Collection Overview

Experimental autoimmune encephalomyelitis (EAE) is an autoimmune disease characterized by central nervous system (CNS) demyelination, focal inflammation, and axonal injury. EAE manifests with ascending flaccid paralysis and can be artificially induced in various animal species via immunization with short peptides containing specific sequences from myelin proteins, in combination with adjuvants to boost the immune response. EAE shares several clinical and pathological features with multiple sclerosis (MS), a chronic human disease also caused by an aberrant immune response against CNS myelin epitopes. For these striking similarities, EAE has become over time the most widely used preclinical model in the MS research field. Although the direct translation of the results collected in this animal model to the human counterpart should be cautious, EAE has been instrumental to elucidate key events underlying MS pathophysiology. Furthermore, several FDA-approved therapies for MS treatment originated directly from EAE studies. Altogether, this evidence corroborates the intrinsic value of the EAE paradigm as an in vivo platform for addressing the multifaceted interplay between the nervous and immune systems in health and disease.

This Methods Collection aims at providing a comprehensive catalog of protocols for EAE induction involving different encephalitogenic peptides as well as experimental animal strains. In addition, EAE-based multi-disciplinary methods to study the dynamics of CNS autoimmunity at both cellular and molecular levels will also be included. Lastly, this special issue will cover those protocols employing EAE for testing innovative anti-inflammatory and re-myelinating therapies.

Articles

Induction and Diverse Assessment Indicators of Experimental Autoimmune Encephalomyelitis
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Induction and Diverse Assessment Indicators of Experimental Autoimmune Encephalomyelitis

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Cited by 2

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2022

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Abstracts

The preparation and immunization of MOG35-55 peptide emulsion for induction of experimental autoimmune encephalomyelitis

Masanori A. Murayama*1

1Department of Animal Models for Human Diseases, Institute of Biomedical Science, Kansai Medical University

Investigation of the Impact of Air Pollution on Autoimmune Effector Cells Utilizing the Adoptive Transfer of MOG-Specific T cells Prior to Particulate Matter Exposure

John Fechner*1

1University of Wisconsin - Madison Department of Surgery Division of Transplantation

The simultaneous Isolation of all principal CNS-resident cell types from adult healthy and EAE mice

Christina Barbara Schroeter*1,

Antonia Henes1,

Alexander M Herrmann1,

Stefanie Bock2,

Christopher Nelke2,

Anna Vogelsang3,

Susann Eichler3,

Philipp Albrecht1,

Sven G Meuth1,

Tobias Ruck1

1Department of Neurology, Medical Faculty, Heinrich Heine University Duesseldorf, Moorenstr. 5, 40225 Duesseldorf, Germany,

2Department of Neurology, Heinrich-Heine University Duesseldorf, Moorenstr. 5, 40225 Duesseldorf, Germany,

3Department of Neurology with Institute of Translational Neurology, University Hospital Muenster, 48149 Muenster, Germany