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Increased Intrathecal B and Plasma Cells in Patients With Anti-IgLON5 Disease: A Case Series

BACKGROUND AND OBJECTIVES: Despite detection of autoantibodies, anti-IgLON5 disease was historically considered a tau-associated neurodegenerative disease, with limited treatment options and detrimental consequences for the patients. Observations in increasing case numbers hint toward underlying inf...

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Autores principales: Strippel, Christine, Heidbreder, Anna, Schulte-Mecklenbeck, Andreas, Korn, Lisanne, Warnecke, Tobias, Melzer, Nico, Wiendl, Heinz, Pawlowski, Matthias, Gross, Catharina C., Kovac, Stjepana
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8759718/
https://www.ncbi.nlm.nih.gov/pubmed/35031586
http://dx.doi.org/10.1212/NXI.0000000000001137
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author Strippel, Christine
Heidbreder, Anna
Schulte-Mecklenbeck, Andreas
Korn, Lisanne
Warnecke, Tobias
Melzer, Nico
Wiendl, Heinz
Pawlowski, Matthias
Gross, Catharina C.
Kovac, Stjepana
author_facet Strippel, Christine
Heidbreder, Anna
Schulte-Mecklenbeck, Andreas
Korn, Lisanne
Warnecke, Tobias
Melzer, Nico
Wiendl, Heinz
Pawlowski, Matthias
Gross, Catharina C.
Kovac, Stjepana
author_sort Strippel, Christine
collection PubMed
description BACKGROUND AND OBJECTIVES: Despite detection of autoantibodies, anti-IgLON5 disease was historically considered a tau-associated neurodegenerative disease, with limited treatment options and detrimental consequences for the patients. Observations in increasing case numbers hint toward underlying inflammatory mechanisms that, early detection provided, open a valuable window of opportunity for therapeutic intervention. We aimed to further substantiate this view by studying the CSF of patients with anti-IgLON5. METHODS: We identified 11 patients with anti-IgLON5 from our database and compared clinical, MRI, and CSF findings with a cohort of 20 patients with progressive supranuclear palsy (PSP) (as a noninflammatory tauopathy) and 22 patients with functional neurologic disorder. RESULTS: Patients with anti-IgLON5 show inflammatory changes in routine CSF analysis, an increase in B-lymphocyte frequency, and the presence of plasma cells in comparison to the PSP-control group and functional neurologic disease controls. Patients with intrathecal plasma cells showed a clinical response to rituximab. DISCUSSION: Our findings indicate the importance of inflammatory mechanisms, in particular in early and acute anti-IgLON5 cases, which may support the use of immune-suppressive treatments in these cases. The main limitation of the study is the small number of cases due to the rarity of the disease.
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spelling pubmed-87597182022-01-20 Increased Intrathecal B and Plasma Cells in Patients With Anti-IgLON5 Disease: A Case Series Strippel, Christine Heidbreder, Anna Schulte-Mecklenbeck, Andreas Korn, Lisanne Warnecke, Tobias Melzer, Nico Wiendl, Heinz Pawlowski, Matthias Gross, Catharina C. Kovac, Stjepana Neurol Neuroimmunol Neuroinflamm Clinical/Scientific Note BACKGROUND AND OBJECTIVES: Despite detection of autoantibodies, anti-IgLON5 disease was historically considered a tau-associated neurodegenerative disease, with limited treatment options and detrimental consequences for the patients. Observations in increasing case numbers hint toward underlying inflammatory mechanisms that, early detection provided, open a valuable window of opportunity for therapeutic intervention. We aimed to further substantiate this view by studying the CSF of patients with anti-IgLON5. METHODS: We identified 11 patients with anti-IgLON5 from our database and compared clinical, MRI, and CSF findings with a cohort of 20 patients with progressive supranuclear palsy (PSP) (as a noninflammatory tauopathy) and 22 patients with functional neurologic disorder. RESULTS: Patients with anti-IgLON5 show inflammatory changes in routine CSF analysis, an increase in B-lymphocyte frequency, and the presence of plasma cells in comparison to the PSP-control group and functional neurologic disease controls. Patients with intrathecal plasma cells showed a clinical response to rituximab. DISCUSSION: Our findings indicate the importance of inflammatory mechanisms, in particular in early and acute anti-IgLON5 cases, which may support the use of immune-suppressive treatments in these cases. The main limitation of the study is the small number of cases due to the rarity of the disease. Lippincott Williams & Wilkins 2022-01-14 /pmc/articles/PMC8759718/ /pubmed/35031586 http://dx.doi.org/10.1212/NXI.0000000000001137 Text en Copyright © 2022 The Author(s). Published by Wolters Kluwer Health, Inc. on behalf of the American Academy of Neurology. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivatives License 4.0 (CC BY-NC-ND) (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which permits downloading and sharing the work provided it is properly cited. The work cannot be changed in any way or used commercially without permission from the journal.
spellingShingle Clinical/Scientific Note
Strippel, Christine
Heidbreder, Anna
Schulte-Mecklenbeck, Andreas
Korn, Lisanne
Warnecke, Tobias
Melzer, Nico
Wiendl, Heinz
Pawlowski, Matthias
Gross, Catharina C.
Kovac, Stjepana
Increased Intrathecal B and Plasma Cells in Patients With Anti-IgLON5 Disease: A Case Series
title Increased Intrathecal B and Plasma Cells in Patients With Anti-IgLON5 Disease: A Case Series
title_full Increased Intrathecal B and Plasma Cells in Patients With Anti-IgLON5 Disease: A Case Series
title_fullStr Increased Intrathecal B and Plasma Cells in Patients With Anti-IgLON5 Disease: A Case Series
title_full_unstemmed Increased Intrathecal B and Plasma Cells in Patients With Anti-IgLON5 Disease: A Case Series
title_short Increased Intrathecal B and Plasma Cells in Patients With Anti-IgLON5 Disease: A Case Series
title_sort increased intrathecal b and plasma cells in patients with anti-iglon5 disease: a case series
topic Clinical/Scientific Note
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8759718/
https://www.ncbi.nlm.nih.gov/pubmed/35031586
http://dx.doi.org/10.1212/NXI.0000000000001137
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