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B Cell Metabolism and Autophagy in Autoimmunity
B cells are central to the pathogenesis of multiple autoimmune diseases, through antigen presentation, cytokine secretion, and the production of autoantibodies. During development and differentiation, B cells undergo drastic changes in their physiology. It is emerging that these are accompanied by e...
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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/PMC8215381/ https://www.ncbi.nlm.nih.gov/pubmed/34163480 http://dx.doi.org/10.3389/fimmu.2021.681105 |
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author | Raza, Iwan G. A. Clarke, Alexander J. |
author_facet | Raza, Iwan G. A. Clarke, Alexander J. |
author_sort | Raza, Iwan G. A. |
collection | PubMed |
description | B cells are central to the pathogenesis of multiple autoimmune diseases, through antigen presentation, cytokine secretion, and the production of autoantibodies. During development and differentiation, B cells undergo drastic changes in their physiology. It is emerging that these are accompanied by equally significant shifts in metabolic phenotype, which may themselves also drive and enforce the functional properties of the cell. The dysfunction of B cells during autoimmunity is characterised by the breaching of tolerogenic checkpoints, and there is developing evidence that the metabolic state of B cells may contribute to this. Determining the metabolic phenotype of B cells in autoimmunity is an area of active study, and is important because intervention by metabolism-altering therapeutic approaches may represent an attractive treatment target. |
format | Online Article Text |
id | pubmed-8215381 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-82153812021-06-22 B Cell Metabolism and Autophagy in Autoimmunity Raza, Iwan G. A. Clarke, Alexander J. Front Immunol Immunology B cells are central to the pathogenesis of multiple autoimmune diseases, through antigen presentation, cytokine secretion, and the production of autoantibodies. During development and differentiation, B cells undergo drastic changes in their physiology. It is emerging that these are accompanied by equally significant shifts in metabolic phenotype, which may themselves also drive and enforce the functional properties of the cell. The dysfunction of B cells during autoimmunity is characterised by the breaching of tolerogenic checkpoints, and there is developing evidence that the metabolic state of B cells may contribute to this. Determining the metabolic phenotype of B cells in autoimmunity is an area of active study, and is important because intervention by metabolism-altering therapeutic approaches may represent an attractive treatment target. Frontiers Media S.A. 2021-06-07 /pmc/articles/PMC8215381/ /pubmed/34163480 http://dx.doi.org/10.3389/fimmu.2021.681105 Text en Copyright © 2021 Raza and Clarke 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 Raza, Iwan G. A. Clarke, Alexander J. B Cell Metabolism and Autophagy in Autoimmunity |
title | B Cell Metabolism and Autophagy in Autoimmunity |
title_full | B Cell Metabolism and Autophagy in Autoimmunity |
title_fullStr | B Cell Metabolism and Autophagy in Autoimmunity |
title_full_unstemmed | B Cell Metabolism and Autophagy in Autoimmunity |
title_short | B Cell Metabolism and Autophagy in Autoimmunity |
title_sort | b cell metabolism and autophagy in autoimmunity |
topic | Immunology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8215381/ https://www.ncbi.nlm.nih.gov/pubmed/34163480 http://dx.doi.org/10.3389/fimmu.2021.681105 |
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