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Continued dysregulation of the B cell lineage promotes multiple sclerosis activity despite disease modifying therapies

A clear understanding of the origin and role of the different subtypes of the B cell lineage involved in the activity or remission of multiple sclerosis (MS) is important for the treatment and follow-up of patients living with this disease. B cells, however, are dynamic and can play an anti-inflamma...

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Autores principales: Londoño, Ana C., Mora, Carlos A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: F1000 Research Limited 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10467621/
https://www.ncbi.nlm.nih.gov/pubmed/37655229
http://dx.doi.org/10.12688/f1000research.74506.3
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author Londoño, Ana C.
Mora, Carlos A.
author_facet Londoño, Ana C.
Mora, Carlos A.
author_sort Londoño, Ana C.
collection PubMed
description A clear understanding of the origin and role of the different subtypes of the B cell lineage involved in the activity or remission of multiple sclerosis (MS) is important for the treatment and follow-up of patients living with this disease. B cells, however, are dynamic and can play an anti-inflammatory or pro-inflammatory role, depending on their milieu. Depletion of B cells has been effective in controlling the progression of MS, but it can have adverse side effects. A better understanding of the role of the B cell subtypes, through the use of surface biomarkers of cellular activity with special attention to the function of memory and other regulatory B cells (Bregs), will be necessary in order to offer specific treatments without inducing undesirable effects.
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spelling pubmed-104676212023-08-31 Continued dysregulation of the B cell lineage promotes multiple sclerosis activity despite disease modifying therapies Londoño, Ana C. Mora, Carlos A. F1000Res Review A clear understanding of the origin and role of the different subtypes of the B cell lineage involved in the activity or remission of multiple sclerosis (MS) is important for the treatment and follow-up of patients living with this disease. B cells, however, are dynamic and can play an anti-inflammatory or pro-inflammatory role, depending on their milieu. Depletion of B cells has been effective in controlling the progression of MS, but it can have adverse side effects. A better understanding of the role of the B cell subtypes, through the use of surface biomarkers of cellular activity with special attention to the function of memory and other regulatory B cells (Bregs), will be necessary in order to offer specific treatments without inducing undesirable effects. F1000 Research Limited 2023-08-01 /pmc/articles/PMC10467621/ /pubmed/37655229 http://dx.doi.org/10.12688/f1000research.74506.3 Text en Copyright: © 2023 Londoño AC and Mora CA https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution Licence, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review
Londoño, Ana C.
Mora, Carlos A.
Continued dysregulation of the B cell lineage promotes multiple sclerosis activity despite disease modifying therapies
title Continued dysregulation of the B cell lineage promotes multiple sclerosis activity despite disease modifying therapies
title_full Continued dysregulation of the B cell lineage promotes multiple sclerosis activity despite disease modifying therapies
title_fullStr Continued dysregulation of the B cell lineage promotes multiple sclerosis activity despite disease modifying therapies
title_full_unstemmed Continued dysregulation of the B cell lineage promotes multiple sclerosis activity despite disease modifying therapies
title_short Continued dysregulation of the B cell lineage promotes multiple sclerosis activity despite disease modifying therapies
title_sort continued dysregulation of the b cell lineage promotes multiple sclerosis activity despite disease modifying therapies
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10467621/
https://www.ncbi.nlm.nih.gov/pubmed/37655229
http://dx.doi.org/10.12688/f1000research.74506.3
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