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Regulatory B Cells: Role in Type 1 Diabetes
Regulatory B cells (Bregs) have an anti-inflammatory role and can suppress autoimmunity, by employing both cytokine secretion and cell-contact mediated mechanisms. Numerous Breg subsets have been described and have overlapping phenotypes in terms of their immune expression markers or cytokine produc...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2021
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8488343/ https://www.ncbi.nlm.nih.gov/pubmed/34616408 http://dx.doi.org/10.3389/fimmu.2021.746187 |
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author | Boldison, Joanne Wong, F. Susan |
author_facet | Boldison, Joanne Wong, F. Susan |
author_sort | Boldison, Joanne |
collection | PubMed |
description | Regulatory B cells (Bregs) have an anti-inflammatory role and can suppress autoimmunity, by employing both cytokine secretion and cell-contact mediated mechanisms. Numerous Breg subsets have been described and have overlapping phenotypes in terms of their immune expression markers or cytokine production. A hallmark feature of Bregs is the secretion of IL-10, although IL-35 and TGFβ−producing B cells have also been identified. To date, few reports have identified an impaired frequency or function of Bregs in individuals with type 1 diabetes; thus our understanding of the role played by these Breg subsets in the pathogenesis of this condition is limited. In this review we will focus on how regulatory B cells are altered in the development of type 1 diabetes, highlighting both frequency and function and discuss both human and animal studies. |
format | Online Article Text |
id | pubmed-8488343 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-84883432021-10-05 Regulatory B Cells: Role in Type 1 Diabetes Boldison, Joanne Wong, F. Susan Front Immunol Immunology Regulatory B cells (Bregs) have an anti-inflammatory role and can suppress autoimmunity, by employing both cytokine secretion and cell-contact mediated mechanisms. Numerous Breg subsets have been described and have overlapping phenotypes in terms of their immune expression markers or cytokine production. A hallmark feature of Bregs is the secretion of IL-10, although IL-35 and TGFβ−producing B cells have also been identified. To date, few reports have identified an impaired frequency or function of Bregs in individuals with type 1 diabetes; thus our understanding of the role played by these Breg subsets in the pathogenesis of this condition is limited. In this review we will focus on how regulatory B cells are altered in the development of type 1 diabetes, highlighting both frequency and function and discuss both human and animal studies. Frontiers Media S.A. 2021-09-20 /pmc/articles/PMC8488343/ /pubmed/34616408 http://dx.doi.org/10.3389/fimmu.2021.746187 Text en Copyright © 2021 Boldison and Wong https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Immunology Boldison, Joanne Wong, F. Susan Regulatory B Cells: Role in Type 1 Diabetes |
title | Regulatory B Cells: Role in Type 1 Diabetes |
title_full | Regulatory B Cells: Role in Type 1 Diabetes |
title_fullStr | Regulatory B Cells: Role in Type 1 Diabetes |
title_full_unstemmed | Regulatory B Cells: Role in Type 1 Diabetes |
title_short | Regulatory B Cells: Role in Type 1 Diabetes |
title_sort | regulatory b cells: role in type 1 diabetes |
topic | Immunology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8488343/ https://www.ncbi.nlm.nih.gov/pubmed/34616408 http://dx.doi.org/10.3389/fimmu.2021.746187 |
work_keys_str_mv | AT boldisonjoanne regulatorybcellsroleintype1diabetes AT wongfsusan regulatorybcellsroleintype1diabetes |