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Multiple Sclerosis: Immunopathology and Treatment Update
The treatment of multiple sclerosis (MS) has changed over the last 20 years. All immunotherapeutic drugs target relapsing remitting MS (RRMS) and it still remains a medical challenge in MS to develop a treatment for progressive forms. The most common injectable disease-modifying therapies in RRMS in...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5532591/ https://www.ncbi.nlm.nih.gov/pubmed/28686222 http://dx.doi.org/10.3390/brainsci7070078 |
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author | Dargahi, Narges Katsara, Maria Tselios, Theodore Androutsou, Maria-Eleni de Courten, Maximilian Matsoukas, John Apostolopoulos, Vasso |
author_facet | Dargahi, Narges Katsara, Maria Tselios, Theodore Androutsou, Maria-Eleni de Courten, Maximilian Matsoukas, John Apostolopoulos, Vasso |
author_sort | Dargahi, Narges |
collection | PubMed |
description | The treatment of multiple sclerosis (MS) has changed over the last 20 years. All immunotherapeutic drugs target relapsing remitting MS (RRMS) and it still remains a medical challenge in MS to develop a treatment for progressive forms. The most common injectable disease-modifying therapies in RRMS include β-interferons 1a or 1b and glatiramer acetate. However, one of the major challenges of injectable disease-modifying therapies has been poor treatment adherence with approximately 50% of patients discontinuing the therapy within the first year. Herein, we go back to the basics to understand the immunopathophysiology of MS to gain insights in the development of new improved drug treatments. We present current disease-modifying therapies (interferons, glatiramer acetate, dimethyl fumarate, teriflunomide, fingolimod, mitoxantrone), humanized monoclonal antibodies (natalizumab, ofatumumab, ocrelizumab, alemtuzumab, daclizumab) and emerging immune modulating approaches (stem cells, DNA vaccines, nanoparticles, altered peptide ligands) for the treatment of MS. |
format | Online Article Text |
id | pubmed-5532591 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-55325912017-08-07 Multiple Sclerosis: Immunopathology and Treatment Update Dargahi, Narges Katsara, Maria Tselios, Theodore Androutsou, Maria-Eleni de Courten, Maximilian Matsoukas, John Apostolopoulos, Vasso Brain Sci Review The treatment of multiple sclerosis (MS) has changed over the last 20 years. All immunotherapeutic drugs target relapsing remitting MS (RRMS) and it still remains a medical challenge in MS to develop a treatment for progressive forms. The most common injectable disease-modifying therapies in RRMS include β-interferons 1a or 1b and glatiramer acetate. However, one of the major challenges of injectable disease-modifying therapies has been poor treatment adherence with approximately 50% of patients discontinuing the therapy within the first year. Herein, we go back to the basics to understand the immunopathophysiology of MS to gain insights in the development of new improved drug treatments. We present current disease-modifying therapies (interferons, glatiramer acetate, dimethyl fumarate, teriflunomide, fingolimod, mitoxantrone), humanized monoclonal antibodies (natalizumab, ofatumumab, ocrelizumab, alemtuzumab, daclizumab) and emerging immune modulating approaches (stem cells, DNA vaccines, nanoparticles, altered peptide ligands) for the treatment of MS. MDPI 2017-07-07 /pmc/articles/PMC5532591/ /pubmed/28686222 http://dx.doi.org/10.3390/brainsci7070078 Text en © 2017 by the authors. 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 (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Review Dargahi, Narges Katsara, Maria Tselios, Theodore Androutsou, Maria-Eleni de Courten, Maximilian Matsoukas, John Apostolopoulos, Vasso Multiple Sclerosis: Immunopathology and Treatment Update |
title | Multiple Sclerosis: Immunopathology and Treatment Update |
title_full | Multiple Sclerosis: Immunopathology and Treatment Update |
title_fullStr | Multiple Sclerosis: Immunopathology and Treatment Update |
title_full_unstemmed | Multiple Sclerosis: Immunopathology and Treatment Update |
title_short | Multiple Sclerosis: Immunopathology and Treatment Update |
title_sort | multiple sclerosis: immunopathology and treatment update |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5532591/ https://www.ncbi.nlm.nih.gov/pubmed/28686222 http://dx.doi.org/10.3390/brainsci7070078 |
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