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Antigen-Specific Treatment Modalities in MS: The Past, the Present, and the Future

Antigen-specific therapy for multiple sclerosis may lead to a more effective therapy by induction of tolerance to a wide range of myelin-derived antigens without hampering the normal surveillance and effector function of the immune system. Numerous attempts to restore tolerance toward myelin-derived...

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Autores principales: Derdelinckx, Judith, Cras, Patrick, Berneman, Zwi N., Cools, Nathalie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7933447/
https://www.ncbi.nlm.nih.gov/pubmed/33679769
http://dx.doi.org/10.3389/fimmu.2021.624685
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author Derdelinckx, Judith
Cras, Patrick
Berneman, Zwi N.
Cools, Nathalie
author_facet Derdelinckx, Judith
Cras, Patrick
Berneman, Zwi N.
Cools, Nathalie
author_sort Derdelinckx, Judith
collection PubMed
description Antigen-specific therapy for multiple sclerosis may lead to a more effective therapy by induction of tolerance to a wide range of myelin-derived antigens without hampering the normal surveillance and effector function of the immune system. Numerous attempts to restore tolerance toward myelin-derived antigens have been made over the past decades, both in animal models of multiple sclerosis and in clinical trials for multiple sclerosis patients. In this review, we will give an overview of the current approaches for antigen-specific therapy that are in clinical development for multiple sclerosis as well provide an insight into the challenges for future antigen-specific treatment strategies for multiple sclerosis.
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spelling pubmed-79334472021-03-06 Antigen-Specific Treatment Modalities in MS: The Past, the Present, and the Future Derdelinckx, Judith Cras, Patrick Berneman, Zwi N. Cools, Nathalie Front Immunol Immunology Antigen-specific therapy for multiple sclerosis may lead to a more effective therapy by induction of tolerance to a wide range of myelin-derived antigens without hampering the normal surveillance and effector function of the immune system. Numerous attempts to restore tolerance toward myelin-derived antigens have been made over the past decades, both in animal models of multiple sclerosis and in clinical trials for multiple sclerosis patients. In this review, we will give an overview of the current approaches for antigen-specific therapy that are in clinical development for multiple sclerosis as well provide an insight into the challenges for future antigen-specific treatment strategies for multiple sclerosis. Frontiers Media S.A. 2021-02-19 /pmc/articles/PMC7933447/ /pubmed/33679769 http://dx.doi.org/10.3389/fimmu.2021.624685 Text en Copyright © 2021 Derdelinckx, Cras, Berneman and Cools http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Immunology
Derdelinckx, Judith
Cras, Patrick
Berneman, Zwi N.
Cools, Nathalie
Antigen-Specific Treatment Modalities in MS: The Past, the Present, and the Future
title Antigen-Specific Treatment Modalities in MS: The Past, the Present, and the Future
title_full Antigen-Specific Treatment Modalities in MS: The Past, the Present, and the Future
title_fullStr Antigen-Specific Treatment Modalities in MS: The Past, the Present, and the Future
title_full_unstemmed Antigen-Specific Treatment Modalities in MS: The Past, the Present, and the Future
title_short Antigen-Specific Treatment Modalities in MS: The Past, the Present, and the Future
title_sort antigen-specific treatment modalities in ms: the past, the present, and the future
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7933447/
https://www.ncbi.nlm.nih.gov/pubmed/33679769
http://dx.doi.org/10.3389/fimmu.2021.624685
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