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Immune-Mediated Neuropathies: Pathophysiology and Management

Dysfunction of the immune system can result in damage of the peripheral nervous system. The immunological mechanisms, which include macrophage infiltration, inflammation and proliferation of Schwann cells, result in variable degrees of demyelination and axonal degeneration. Aetiology is diverse and,...

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Autores principales: Shastri, Abhishek, Al Aiyan, Ahmad, Kishore, Uday, Farrugia, Maria Elena
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10139406/
https://www.ncbi.nlm.nih.gov/pubmed/37108447
http://dx.doi.org/10.3390/ijms24087288
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author Shastri, Abhishek
Al Aiyan, Ahmad
Kishore, Uday
Farrugia, Maria Elena
author_facet Shastri, Abhishek
Al Aiyan, Ahmad
Kishore, Uday
Farrugia, Maria Elena
author_sort Shastri, Abhishek
collection PubMed
description Dysfunction of the immune system can result in damage of the peripheral nervous system. The immunological mechanisms, which include macrophage infiltration, inflammation and proliferation of Schwann cells, result in variable degrees of demyelination and axonal degeneration. Aetiology is diverse and, in some cases, may be precipitated by infection. Various animal models have contributed and helped to elucidate the pathophysiological mechanisms in acute and chronic inflammatory polyradiculoneuropathies (Guillain–Barre Syndrome and chronic inflammatory demyelinating polyradiculoneuropathy, respectively). The presence of specific anti-glycoconjugate antibodies indicates an underlying process of molecular mimicry and sometimes assists in the classification of these disorders, which often merely supports the clinical diagnosis. Now, the electrophysiological presence of conduction blocks is another important factor in characterizing another subgroup of treatable motor neuropathies (multifocal motor neuropathy with conduction block), which is distinct from Lewis–Sumner syndrome (multifocal acquired demyelinating sensory and motor neuropathy) in its response to treatment modalities as well as electrophysiological features. Furthermore, paraneoplastic neuropathies are also immune-mediated and are the result of an immune reaction to tumour cells that express onconeural antigens and mimic molecules expressed on the surface of neurons. The detection of specific paraneoplastic antibodies often assists the clinician in the investigation of an underlying, sometimes specific, malignancy. This review aims to discuss the immunological and pathophysiological mechanisms that are thought to be crucial in the aetiology of dysimmune neuropathies as well as their individual electrophysiological characteristics, their laboratory features and existing treatment options. Here, we aim to present a balance of discussion from these diverse angles that may be helpful in categorizing disease and establishing prognosis.
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spelling pubmed-101394062023-04-28 Immune-Mediated Neuropathies: Pathophysiology and Management Shastri, Abhishek Al Aiyan, Ahmad Kishore, Uday Farrugia, Maria Elena Int J Mol Sci Review Dysfunction of the immune system can result in damage of the peripheral nervous system. The immunological mechanisms, which include macrophage infiltration, inflammation and proliferation of Schwann cells, result in variable degrees of demyelination and axonal degeneration. Aetiology is diverse and, in some cases, may be precipitated by infection. Various animal models have contributed and helped to elucidate the pathophysiological mechanisms in acute and chronic inflammatory polyradiculoneuropathies (Guillain–Barre Syndrome and chronic inflammatory demyelinating polyradiculoneuropathy, respectively). The presence of specific anti-glycoconjugate antibodies indicates an underlying process of molecular mimicry and sometimes assists in the classification of these disorders, which often merely supports the clinical diagnosis. Now, the electrophysiological presence of conduction blocks is another important factor in characterizing another subgroup of treatable motor neuropathies (multifocal motor neuropathy with conduction block), which is distinct from Lewis–Sumner syndrome (multifocal acquired demyelinating sensory and motor neuropathy) in its response to treatment modalities as well as electrophysiological features. Furthermore, paraneoplastic neuropathies are also immune-mediated and are the result of an immune reaction to tumour cells that express onconeural antigens and mimic molecules expressed on the surface of neurons. The detection of specific paraneoplastic antibodies often assists the clinician in the investigation of an underlying, sometimes specific, malignancy. This review aims to discuss the immunological and pathophysiological mechanisms that are thought to be crucial in the aetiology of dysimmune neuropathies as well as their individual electrophysiological characteristics, their laboratory features and existing treatment options. Here, we aim to present a balance of discussion from these diverse angles that may be helpful in categorizing disease and establishing prognosis. MDPI 2023-04-14 /pmc/articles/PMC10139406/ /pubmed/37108447 http://dx.doi.org/10.3390/ijms24087288 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Shastri, Abhishek
Al Aiyan, Ahmad
Kishore, Uday
Farrugia, Maria Elena
Immune-Mediated Neuropathies: Pathophysiology and Management
title Immune-Mediated Neuropathies: Pathophysiology and Management
title_full Immune-Mediated Neuropathies: Pathophysiology and Management
title_fullStr Immune-Mediated Neuropathies: Pathophysiology and Management
title_full_unstemmed Immune-Mediated Neuropathies: Pathophysiology and Management
title_short Immune-Mediated Neuropathies: Pathophysiology and Management
title_sort immune-mediated neuropathies: pathophysiology and management
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10139406/
https://www.ncbi.nlm.nih.gov/pubmed/37108447
http://dx.doi.org/10.3390/ijms24087288
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