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Visualizing Impairment of the Endothelial and Glial Barriers of the Neurovascular Unit during Experimental Autoimmune Encephalomyelitis In Vivo
Published on: March 26, 2019
Novel methods for neural IgG characterization and validation in autoimmune neurologic disorders
Michael Gilligan1, Andrew McKeon2
1Departments of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, MN, USA; Department of Neurology, St Vincent's University Hospital, Dublin, Ireland.
Neural autoantibody discovery has expanded significantly, with over 50 antibodies identified. Novel immune-profiling assays like protein array and phage immunoprecipitation sequencing (PhIP-Seq) accelerate this process for autoimmune neurology.
Area of Science:
- Neurology
- Immunology
- Biotechnology
Background:
- Neural autoantibody testing is crucial for diagnosing autoimmune neurologic disorders.
- Over 50 disease-specific neural antibodies have been identified in the last 40 years.
- Traditional methods for antibody discovery are being enhanced by new technologies.
Purpose of the Study:
- To review traditional and novel methods for neural autoantibody discovery.
- To emphasize the role of protein array and phage immunoprecipitation sequencing (PhIP-Seq) in antibody discovery.
- To discuss the advantages, limitations, and future applications of these platforms in autoimmune neurology.
Main Methods:
- Review of existing literature on neural autoantibody discovery.
- Focus on immune-profiling assays: protein array and PhIP-Seq.
- Analysis of the integration of these novel methods into discovery workflows.
Main Results:
- The number of identified neural antibodies has grown substantially.
- Protein array and PhIP-Seq have expedited the discovery of new neural autoantibodies.
- These advanced techniques are key to identifying recent targets.
Conclusions:
- Protein array and PhIP-Seq represent significant advancements in neural autoantibody discovery.
- These platforms offer powerful tools for advancing autoimmune neurology research.
- Further exploration of these methods will likely yield more disease-specific antibodies.
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