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B Cell Activation and Escape of Tolerance Checkpoints: Recent Insights from Studying Autoreactive B Cells

Autoreactive B cells are key drivers of pathogenic processes in autoimmune diseases by the production of autoantibodies, secretion of cytokines, and presentation of autoantigens to T cells. However, the mechanisms that underlie the development of autoreactive B cells are not well understood. Here, w...

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Detalles Bibliográficos
Autores principales: Bonasia, Carlo G., Abdulahad, Wayel H., Rutgers, Abraham, Heeringa, Peter, Bos, Nicolaas A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8152463/
https://www.ncbi.nlm.nih.gov/pubmed/34068035
http://dx.doi.org/10.3390/cells10051190
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author Bonasia, Carlo G.
Abdulahad, Wayel H.
Rutgers, Abraham
Heeringa, Peter
Bos, Nicolaas A.
author_facet Bonasia, Carlo G.
Abdulahad, Wayel H.
Rutgers, Abraham
Heeringa, Peter
Bos, Nicolaas A.
author_sort Bonasia, Carlo G.
collection PubMed
description Autoreactive B cells are key drivers of pathogenic processes in autoimmune diseases by the production of autoantibodies, secretion of cytokines, and presentation of autoantigens to T cells. However, the mechanisms that underlie the development of autoreactive B cells are not well understood. Here, we review recent studies leveraging novel techniques to identify and characterize (auto)antigen-specific B cells. The insights gained from such studies pertaining to the mechanisms involved in the escape of tolerance checkpoints and the activation of autoreactive B cells are discussed. In addition, we briefly highlight potential therapeutic strategies to target and eliminate autoreactive B cells in autoimmune diseases.
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spelling pubmed-81524632021-05-27 B Cell Activation and Escape of Tolerance Checkpoints: Recent Insights from Studying Autoreactive B Cells Bonasia, Carlo G. Abdulahad, Wayel H. Rutgers, Abraham Heeringa, Peter Bos, Nicolaas A. Cells Review Autoreactive B cells are key drivers of pathogenic processes in autoimmune diseases by the production of autoantibodies, secretion of cytokines, and presentation of autoantigens to T cells. However, the mechanisms that underlie the development of autoreactive B cells are not well understood. Here, we review recent studies leveraging novel techniques to identify and characterize (auto)antigen-specific B cells. The insights gained from such studies pertaining to the mechanisms involved in the escape of tolerance checkpoints and the activation of autoreactive B cells are discussed. In addition, we briefly highlight potential therapeutic strategies to target and eliminate autoreactive B cells in autoimmune diseases. MDPI 2021-05-13 /pmc/articles/PMC8152463/ /pubmed/34068035 http://dx.doi.org/10.3390/cells10051190 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Bonasia, Carlo G.
Abdulahad, Wayel H.
Rutgers, Abraham
Heeringa, Peter
Bos, Nicolaas A.
B Cell Activation and Escape of Tolerance Checkpoints: Recent Insights from Studying Autoreactive B Cells
title B Cell Activation and Escape of Tolerance Checkpoints: Recent Insights from Studying Autoreactive B Cells
title_full B Cell Activation and Escape of Tolerance Checkpoints: Recent Insights from Studying Autoreactive B Cells
title_fullStr B Cell Activation and Escape of Tolerance Checkpoints: Recent Insights from Studying Autoreactive B Cells
title_full_unstemmed B Cell Activation and Escape of Tolerance Checkpoints: Recent Insights from Studying Autoreactive B Cells
title_short B Cell Activation and Escape of Tolerance Checkpoints: Recent Insights from Studying Autoreactive B Cells
title_sort b cell activation and escape of tolerance checkpoints: recent insights from studying autoreactive b cells
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8152463/
https://www.ncbi.nlm.nih.gov/pubmed/34068035
http://dx.doi.org/10.3390/cells10051190
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