The role of the complement system in Multiple Sclerosis: A review

The complement system has been involved in the pathogenesis of multiple neuroinflammatory and neurodegenerative conditions. In this review, we evaluated the possible role of complement activation in multiple sclerosis (MS) with a focus in progressive MS, where the disease pathogenesis remains to be...

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Main Authors: Nil Saez-Calveras, Olaf Stuve
Format: Article
Language:English
Published: Frontiers Media S.A. 2022-08-01
Series:Frontiers in Immunology
Subjects:
Online Access:https://www.frontiersin.org/articles/10.3389/fimmu.2022.970486/full
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author Nil Saez-Calveras
Olaf Stuve
Olaf Stuve
author_facet Nil Saez-Calveras
Olaf Stuve
Olaf Stuve
author_sort Nil Saez-Calveras
collection DOAJ
description The complement system has been involved in the pathogenesis of multiple neuroinflammatory and neurodegenerative conditions. In this review, we evaluated the possible role of complement activation in multiple sclerosis (MS) with a focus in progressive MS, where the disease pathogenesis remains to be fully elucidated and treatment options are limited. The evidence for the involvement of the complement system in the white matter plaques and gray matter lesions of MS stems from immunohistochemical analysis of post-mortem MS brains, in vivo serum and cerebrospinal fluid biomarker studies, and animal models of Experimental Autoimmune Encephalomyelitis (EAE). Complement knock-out studies in these animal models have revealed that this system may have a “double-edge sword” effect in MS. On the one hand, complement proteins may aid in promoting the clearance of myelin degradation products and other debris through myeloid cell-mediated phagocytosis. On the other, its aberrant activation may lead to demyelination at the rim of progressive MS white matter lesions as well as synapse loss in the gray matter. The complement system may also interact with known risk factors of MS, including as Epstein Barr Virus (EBV) infection, and perpetuate the activation of CNS self-reactive B cell populations. With the mounting evidence for the involvement of complement in MS, the development of complement modulating therapies for this condition is appealing. Herein, we also reviewed the pharmacological complement inhibitors that have been tested in MS animal models as well as in clinical trials for other neurologic diseases. The potential use of these agents, such as the C5-binding antibody eculizumab in MS will require a detailed understanding of the role of the different complement effectors in this disease and the development of better CNS delivery strategies for these compounds.
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spelling doaj.art-13af2bb7f080468c9a4383d466c4df4d2022-12-22T01:35:06ZengFrontiers Media S.A.Frontiers in Immunology1664-32242022-08-011310.3389/fimmu.2022.970486970486The role of the complement system in Multiple Sclerosis: A reviewNil Saez-Calveras0Olaf Stuve1Olaf Stuve2Department of Neurology, University of Texas Southwestern Medical Center, Dallas, TX, United StatesDepartment of Neurology, University of Texas Southwestern Medical Center, Dallas, TX, United StatesNeurology Section, Veterans Affairs (VA) North Texas Health Care System, Dallas, TX, United StatesThe complement system has been involved in the pathogenesis of multiple neuroinflammatory and neurodegenerative conditions. In this review, we evaluated the possible role of complement activation in multiple sclerosis (MS) with a focus in progressive MS, where the disease pathogenesis remains to be fully elucidated and treatment options are limited. The evidence for the involvement of the complement system in the white matter plaques and gray matter lesions of MS stems from immunohistochemical analysis of post-mortem MS brains, in vivo serum and cerebrospinal fluid biomarker studies, and animal models of Experimental Autoimmune Encephalomyelitis (EAE). Complement knock-out studies in these animal models have revealed that this system may have a “double-edge sword” effect in MS. On the one hand, complement proteins may aid in promoting the clearance of myelin degradation products and other debris through myeloid cell-mediated phagocytosis. On the other, its aberrant activation may lead to demyelination at the rim of progressive MS white matter lesions as well as synapse loss in the gray matter. The complement system may also interact with known risk factors of MS, including as Epstein Barr Virus (EBV) infection, and perpetuate the activation of CNS self-reactive B cell populations. With the mounting evidence for the involvement of complement in MS, the development of complement modulating therapies for this condition is appealing. Herein, we also reviewed the pharmacological complement inhibitors that have been tested in MS animal models as well as in clinical trials for other neurologic diseases. The potential use of these agents, such as the C5-binding antibody eculizumab in MS will require a detailed understanding of the role of the different complement effectors in this disease and the development of better CNS delivery strategies for these compounds.https://www.frontiersin.org/articles/10.3389/fimmu.2022.970486/fullcomplement systemmultiple sclerosisprogressive multiple sclerosisEAE (experimental autoimmune encephalomyelitis)synaptic pruningepstein barr virus
spellingShingle Nil Saez-Calveras
Olaf Stuve
Olaf Stuve
The role of the complement system in Multiple Sclerosis: A review
Frontiers in Immunology
complement system
multiple sclerosis
progressive multiple sclerosis
EAE (experimental autoimmune encephalomyelitis)
synaptic pruning
epstein barr virus
title The role of the complement system in Multiple Sclerosis: A review
title_full The role of the complement system in Multiple Sclerosis: A review
title_fullStr The role of the complement system in Multiple Sclerosis: A review
title_full_unstemmed The role of the complement system in Multiple Sclerosis: A review
title_short The role of the complement system in Multiple Sclerosis: A review
title_sort role of the complement system in multiple sclerosis a review
topic complement system
multiple sclerosis
progressive multiple sclerosis
EAE (experimental autoimmune encephalomyelitis)
synaptic pruning
epstein barr virus
url https://www.frontiersin.org/articles/10.3389/fimmu.2022.970486/full
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