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Scientific Session - Immunopathology
Scientific
Scientific
1:30 pm
22 February 2025
Meeting Room 104
Discipline Streams
Immunopathology
Session Scientific Program
John Soltys1
1University of South Alabama
Autoantibody testing has become a staple in diagnosing a spectrum of neuroinflammatory disorders. Yet, antibody-associated neurological disorders remain some of the most over-diagnosed and under-diagnosed neurological disorders. This talk explores the pearls and pitfalls of autoantibody testing that contribute to this paradox.
Autoantibody testing has become a staple in diagnosing a spectrum of neuroinflammatory disorders. Yet, antibody-associated neurological disorders remain some of the most over-diagnosed and under-diagnosed neurological disorders. This talk explores the pearls and pitfalls of autoantibody testing that contribute to this paradox.
A Neurologist’s approach to Autoimmune encephalitis
Christine Bundell1
1PathWest Laboratory Medicine
Autoantibodies were first associated with inclusion body myositis (IBM) in 2011 following the identification of B cells and plasma cells in IBM muscle biopsies. Cytosolic 5”-nucleotidase 1A (C5N1A) was subsequently identified as a target antigen.
1PathWest Laboratory Medicine
Autoantibodies were first associated with inclusion body myositis (IBM) in 2011 following the identification of B cells and plasma cells in IBM muscle biopsies. Cytosolic 5”-nucleotidase 1A (C5N1A) was subsequently identified as a target antigen.
Since the antibody was first identified, testing by ELISA and immunoblot has become available. Seventeen participants are enrolled in in the RCPA Quality Assurance Myositis and Scleroderma Antibody program which includes C5N1A antibody testing.
PathWest Laboratory Medicine (PWLM) performs an in house IVD ELISA using details reported by Greenburg in 2014. PWLM receives samples from WA, interstate and from New Zealand. 883 samples, from 841 patients have been tested for C5NIA antibodies over the last 38 months 19% of patients were C5N1A antibody positive. Among 13 patients from Western Australia with positive C5N1A antibody results, 62% had an established diagnosis of IBM. Where clinical suspicion of IBM is high and C5N1A antibodies are positive, invasive muscle biopsy may be not be required.