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Induction or aggravation of other immune-mediated disorders by disease-modifying therapy in treatment of multiple sclerosis

Interferon beta (IFN-β) and glatiramer acetate (GA) are the primary therapeutic immunomodulatory agents that interfere with relapsing-remitting multiple sclerosis (RRMS), and the most commonly-used drugs as well. Induction or aggravation of other immune-mediated diseases has been reported following...

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Detalles Bibliográficos
Autores principales: Baghbanian, Seyed Mohammad, Sahraian, Mohammad Ali
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Tehran University of Medical Sciences 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6420690/
https://www.ncbi.nlm.nih.gov/pubmed/30886680
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author Baghbanian, Seyed Mohammad
Sahraian, Mohammad Ali
author_facet Baghbanian, Seyed Mohammad
Sahraian, Mohammad Ali
author_sort Baghbanian, Seyed Mohammad
collection PubMed
description Interferon beta (IFN-β) and glatiramer acetate (GA) are the primary therapeutic immunomodulatory agents that interfere with relapsing-remitting multiple sclerosis (RRMS), and the most commonly-used drugs as well. Induction or aggravation of other immune-mediated diseases has been reported following INF-β administration. We have reviewed the reported cases to notify the treating physicians about these rare adverse events. Although co-morbid autoimmune disorders have been reported in patients with MS, the pro-inflammatory role of disease-modifying drugs, especially INF-β, could affect and enhance this co-occurrence. Clinical or laboratory autoimmunity histories suggest the use of GA over INF-β as the treatment of choice.
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spelling pubmed-64206902019-03-18 Induction or aggravation of other immune-mediated disorders by disease-modifying therapy in treatment of multiple sclerosis Baghbanian, Seyed Mohammad Sahraian, Mohammad Ali Iran J Neurol Review Article Interferon beta (IFN-β) and glatiramer acetate (GA) are the primary therapeutic immunomodulatory agents that interfere with relapsing-remitting multiple sclerosis (RRMS), and the most commonly-used drugs as well. Induction or aggravation of other immune-mediated diseases has been reported following INF-β administration. We have reviewed the reported cases to notify the treating physicians about these rare adverse events. Although co-morbid autoimmune disorders have been reported in patients with MS, the pro-inflammatory role of disease-modifying drugs, especially INF-β, could affect and enhance this co-occurrence. Clinical or laboratory autoimmunity histories suggest the use of GA over INF-β as the treatment of choice. Tehran University of Medical Sciences 2018-07-06 /pmc/articles/PMC6420690/ /pubmed/30886680 Text en Copyright © 2015 Iranian Neurological Association, and Tehran University of Medical Sciences This is an Open Access article distributed under the terms of the Creative Commons Attribution License, (http://creativecommons.org/licenses/by/3.0/) which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review Article
Baghbanian, Seyed Mohammad
Sahraian, Mohammad Ali
Induction or aggravation of other immune-mediated disorders by disease-modifying therapy in treatment of multiple sclerosis
title Induction or aggravation of other immune-mediated disorders by disease-modifying therapy in treatment of multiple sclerosis
title_full Induction or aggravation of other immune-mediated disorders by disease-modifying therapy in treatment of multiple sclerosis
title_fullStr Induction or aggravation of other immune-mediated disorders by disease-modifying therapy in treatment of multiple sclerosis
title_full_unstemmed Induction or aggravation of other immune-mediated disorders by disease-modifying therapy in treatment of multiple sclerosis
title_short Induction or aggravation of other immune-mediated disorders by disease-modifying therapy in treatment of multiple sclerosis
title_sort induction or aggravation of other immune-mediated disorders by disease-modifying therapy in treatment of multiple sclerosis
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6420690/
https://www.ncbi.nlm.nih.gov/pubmed/30886680
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