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Intravenous Immunoglobulin Treatment in Multifocal Motor Neuropathy

INTRODUCTION: Multifocal motor neuropathy (MMN) is characterized by asymmetric weakness of limbs and the electrophysiological finding of conduction block in motor nerves. Conduction block is the inability of nerves to propagate action potentials and is probably caused by immune-mediated dysfunction...

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Autores principales: van der Pol, W.-Ludo, Cats, Elisabeth A., van den Berg, Leonard H.
Formato: Texto
Lenguaje:English
Publicado: Springer US 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2883087/
https://www.ncbi.nlm.nih.gov/pubmed/20405181
http://dx.doi.org/10.1007/s10875-010-9408-3
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author van der Pol, W.-Ludo
Cats, Elisabeth A.
van den Berg, Leonard H.
author_facet van der Pol, W.-Ludo
Cats, Elisabeth A.
van den Berg, Leonard H.
author_sort van der Pol, W.-Ludo
collection PubMed
description INTRODUCTION: Multifocal motor neuropathy (MMN) is characterized by asymmetric weakness of limbs and the electrophysiological finding of conduction block in motor nerves. Conduction block is the inability of nerves to propagate action potentials and is probably caused by immune-mediated dysfunction of the axon at the nodes of Ranvier or the myelin sheath. MMN immune pathogenesis has not been elucidated. RESULTS: In approximately 50% of all patients, IgM antibodies that bind to the glycolipid GM1, which is abundantly expressed in peripheral motor nerves, can be detected. A recent study showed an association with HLA-DRB1*15, and virtually all patients respond to treatment with intravenous immunoglobulin (IVIG) in at least the early stages of the disease. CONCLUSION: This review aims at providing a concise overview of what is known about MMN pathogenesis, and how the beneficial effect of IVIG might be explained.
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spelling pubmed-28830872010-06-21 Intravenous Immunoglobulin Treatment in Multifocal Motor Neuropathy van der Pol, W.-Ludo Cats, Elisabeth A. van den Berg, Leonard H. J Clin Immunol Article INTRODUCTION: Multifocal motor neuropathy (MMN) is characterized by asymmetric weakness of limbs and the electrophysiological finding of conduction block in motor nerves. Conduction block is the inability of nerves to propagate action potentials and is probably caused by immune-mediated dysfunction of the axon at the nodes of Ranvier or the myelin sheath. MMN immune pathogenesis has not been elucidated. RESULTS: In approximately 50% of all patients, IgM antibodies that bind to the glycolipid GM1, which is abundantly expressed in peripheral motor nerves, can be detected. A recent study showed an association with HLA-DRB1*15, and virtually all patients respond to treatment with intravenous immunoglobulin (IVIG) in at least the early stages of the disease. CONCLUSION: This review aims at providing a concise overview of what is known about MMN pathogenesis, and how the beneficial effect of IVIG might be explained. Springer US 2010-04-20 2010 /pmc/articles/PMC2883087/ /pubmed/20405181 http://dx.doi.org/10.1007/s10875-010-9408-3 Text en © The Author(s) 2010 https://creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution Noncommercial License which permits any noncommercial use, distribution, and reproduction in any medium, provided the original author(s) and source are credited.
spellingShingle Article
van der Pol, W.-Ludo
Cats, Elisabeth A.
van den Berg, Leonard H.
Intravenous Immunoglobulin Treatment in Multifocal Motor Neuropathy
title Intravenous Immunoglobulin Treatment in Multifocal Motor Neuropathy
title_full Intravenous Immunoglobulin Treatment in Multifocal Motor Neuropathy
title_fullStr Intravenous Immunoglobulin Treatment in Multifocal Motor Neuropathy
title_full_unstemmed Intravenous Immunoglobulin Treatment in Multifocal Motor Neuropathy
title_short Intravenous Immunoglobulin Treatment in Multifocal Motor Neuropathy
title_sort intravenous immunoglobulin treatment in multifocal motor neuropathy
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2883087/
https://www.ncbi.nlm.nih.gov/pubmed/20405181
http://dx.doi.org/10.1007/s10875-010-9408-3
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