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Age-associated B cells in autoimmune diseases

Age-associated B cells (ABCs) are a transcriptionally and functionally unique B cell population. In addition to arising with age and following infection, ABCs are expanded during autoimmune disease, including those with systemic lupus erythematosus, multiple sclerosis, and rheumatoid arthritis. The...

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Detalles Bibliográficos
Autores principales: Mouat, Isobel C., Goldberg, Erin, Horwitz, Marc S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer International Publishing 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9263041/
https://www.ncbi.nlm.nih.gov/pubmed/35798993
http://dx.doi.org/10.1007/s00018-022-04433-9
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author Mouat, Isobel C.
Goldberg, Erin
Horwitz, Marc S.
author_facet Mouat, Isobel C.
Goldberg, Erin
Horwitz, Marc S.
author_sort Mouat, Isobel C.
collection PubMed
description Age-associated B cells (ABCs) are a transcriptionally and functionally unique B cell population. In addition to arising with age and following infection, ABCs are expanded during autoimmune disease, including those with systemic lupus erythematosus, multiple sclerosis, and rheumatoid arthritis. The exact nature of how ABCs impact disease remains unclear. Here, we review what is known regarding ABC development and distribution during diseases including systemic lupus erythematosus, multiple sclerosis, and rheumatoid arthritis. We discuss possible mechanisms by which ABCs could contribute to disease, including the production of cytokines and autoantibodies or stimulation of T cells. Finally, we speculate on how ABCs might act as mediators between sex, infection, and autoimmune disease, and discuss avenues for further research.
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spelling pubmed-92630412022-07-08 Age-associated B cells in autoimmune diseases Mouat, Isobel C. Goldberg, Erin Horwitz, Marc S. Cell Mol Life Sci Review Age-associated B cells (ABCs) are a transcriptionally and functionally unique B cell population. In addition to arising with age and following infection, ABCs are expanded during autoimmune disease, including those with systemic lupus erythematosus, multiple sclerosis, and rheumatoid arthritis. The exact nature of how ABCs impact disease remains unclear. Here, we review what is known regarding ABC development and distribution during diseases including systemic lupus erythematosus, multiple sclerosis, and rheumatoid arthritis. We discuss possible mechanisms by which ABCs could contribute to disease, including the production of cytokines and autoantibodies or stimulation of T cells. Finally, we speculate on how ABCs might act as mediators between sex, infection, and autoimmune disease, and discuss avenues for further research. Springer International Publishing 2022-07-07 2022 /pmc/articles/PMC9263041/ /pubmed/35798993 http://dx.doi.org/10.1007/s00018-022-04433-9 Text en © The Author(s), under exclusive licence to Springer Nature Switzerland AG 2022 This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic.
spellingShingle Review
Mouat, Isobel C.
Goldberg, Erin
Horwitz, Marc S.
Age-associated B cells in autoimmune diseases
title Age-associated B cells in autoimmune diseases
title_full Age-associated B cells in autoimmune diseases
title_fullStr Age-associated B cells in autoimmune diseases
title_full_unstemmed Age-associated B cells in autoimmune diseases
title_short Age-associated B cells in autoimmune diseases
title_sort age-associated b cells in autoimmune diseases
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9263041/
https://www.ncbi.nlm.nih.gov/pubmed/35798993
http://dx.doi.org/10.1007/s00018-022-04433-9
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