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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...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer International Publishing
2022
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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. |
format | Online Article Text |
id | pubmed-9263041 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Springer International Publishing |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT mouatisobelc ageassociatedbcellsinautoimmunediseases AT goldbergerin ageassociatedbcellsinautoimmunediseases AT horwitzmarcs ageassociatedbcellsinautoimmunediseases |