Literature DB >> 33962172

Autoantibodies to cortactin and agrin in sera of patients with myasthenia gravis.

Kathrin Doppler1, Antonia Hemprich2, Axel Haarmann3, Isabel Brecht4, Maximilian Franke5, Stephan Kröger6, Carmen Villmann7, Claudia Sommer8.   

Abstract

Autoantibodies against agrin and cortactin have been described in patients with myasthenia gravis. To further validate and characterize these autoantibodies, sera and/or plasma exchange material of 135 patients with myasthenia gravis were screened for anti-agrin or anti-cortactin autoantibodies. Autoantibodies against cortactin were detected in three patients and two controls and could be confirmed by cell-based assays using cortactin-transfected human embryonic kidney cells in both controls and one patient, but were not detectable in follow-up sera of the three patients. We did not detect any autoantibodies against agrin. The clinical phenotype of anti-cortactin-positive patients varied, arguing against a relevant pathogenic role.
Copyright © 2021 Elsevier B.V. All rights reserved.

Entities:  

Keywords:  Agrin; Autoantibody; Cortactin; Myasthenia gravis

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Year:  2021        PMID: 33962172     DOI: 10.1016/j.jneuroim.2021.577588

Source DB:  PubMed          Journal:  J Neuroimmunol        ISSN: 0165-5728            Impact factor:   3.478


  1 in total

1.  Severe congenital myasthenic syndromes caused by agrin mutations affecting secretion by motoneurons.

Authors:  Arnaud Jacquier; Valérie Risson; Thomas Simonet; Florine Roussange; Nicolas Lacoste; Shams Ribault; Julien Carras; Julian Theuriet; Emmanuelle Girard; Isabelle Grosjean; Laure Le Goff; Stephan Kröger; Julia Meltoranta; Stéphanie Bauché; Damien Sternberg; Emmanuel Fournier; Anna Kostera-Pruszczyk; Emily O'Connor; Bruno Eymard; Hanns Lochmüller; Cécile Martinat; Laurent Schaeffer
Journal:  Acta Neuropathol       Date:  2022-08-10       Impact factor: 15.887

  1 in total

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