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Tryptophan immunoadsorption for the treatment of autoimmune encephalitis

W. Köhler*, S. Ehrlich, C. Dohmen, M. Haubitz, F. Hoffmann, S. Schmidt, R. Klingel, A. Kraft, T. Neumann-Haefelin, H. Topka, O. Stich, A. Baumgartner, C. Fassbender

*Corresponding author for this work

Abstract

Background and purpose: Detection of autoantibodies against neuronal surface antigens and their correlation with the pattern and severity of symptoms led to the definition of new autoimmune-mediated forms of encephalitis and was essential for the initiation of immunotherapies including plasma exchange. The elimination of autoantibodies using selective immunoadsorption (IA) is a pathophysiologically guided therapeutic approach but has not yet been evaluated in a separate analysis. Methods: A retrospective analysis was performed of patients with autoimmune encephalitis who were treated with tryptophan IA in six neurological clinics between 2009 and 2013. The modified Rankin scale (mRS) was used to evaluate neurological status before and after IA. Results: Data on 13 patients were documented. Twelve patients were positive for specific autoantibodies (NMDA-R, GABA, GAD, Lgl1). Patients received a series of a median of six IA treatments. Median mRS of all patients was 3.0 before IA and 2.0 after IA (P < 0.001). Eleven patients improved by at least one point in mRS after IA. Conclusion: For autoimmune-mediated forms of encephalitis rapid elimination of autoantibodies with selective IA seems to be an effective therapeutic option as part of multimodal immune therapy.

Original languageEnglish
JournalEuropean Journal of Neurology
Volume22
Issue number1
Pages (from-to)203-206
Number of pages4
ISSN1351-5101
DOIs
Publication statusPublished - 01.01.2015

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Research Areas and Centers

  • Health Sciences
  • Academic Focus: Center for Infection and Inflammation Research (ZIEL)

DFG Research Classification Scheme

  • 2.23-06 Molecular and Cellular Neurology and Neuropathology
  • 2.22-22 Clinical Immunology and Allergology
  • 2.23-07 Clinical Neurology, Neurosurgery and Neuroradiology
  • 2.21-05 Immunology

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