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The Role of B Cells and B Cell Therapies in Immune-Mediated Liver Diseases

B cells form a branch of the adaptive immune system, essential for the body’s immune defense against pathogens. B cell dysfunction has been implicated in the pathogenesis of immune mediated liver diseases including autoimmune hepatitis, IgG4-related hepatobiliary disease, primary biliary cholangitis...

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Detalles Bibliográficos
Autores principales: Cargill, Tamsin, Culver, Emma L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8079753/
https://www.ncbi.nlm.nih.gov/pubmed/33936097
http://dx.doi.org/10.3389/fimmu.2021.661196
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author Cargill, Tamsin
Culver, Emma L.
author_facet Cargill, Tamsin
Culver, Emma L.
author_sort Cargill, Tamsin
collection PubMed
description B cells form a branch of the adaptive immune system, essential for the body’s immune defense against pathogens. B cell dysfunction has been implicated in the pathogenesis of immune mediated liver diseases including autoimmune hepatitis, IgG4-related hepatobiliary disease, primary biliary cholangitis and primary sclerosing cholangitis. B cells may initiate and maintain immune related liver diseases in several ways including the production of autoantibodies and the activation of T cells via antigen presentation or cytokine production. Here we comprehensively review current knowledge on B cell mechanisms in immune mediated liver diseases, exploring disease pathogenesis, B cell therapies, and novel treatment targets. We identify key areas where future research should focus to enable the development of targeted B cell therapies.
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spelling pubmed-80797532021-04-29 The Role of B Cells and B Cell Therapies in Immune-Mediated Liver Diseases Cargill, Tamsin Culver, Emma L. Front Immunol Immunology B cells form a branch of the adaptive immune system, essential for the body’s immune defense against pathogens. B cell dysfunction has been implicated in the pathogenesis of immune mediated liver diseases including autoimmune hepatitis, IgG4-related hepatobiliary disease, primary biliary cholangitis and primary sclerosing cholangitis. B cells may initiate and maintain immune related liver diseases in several ways including the production of autoantibodies and the activation of T cells via antigen presentation or cytokine production. Here we comprehensively review current knowledge on B cell mechanisms in immune mediated liver diseases, exploring disease pathogenesis, B cell therapies, and novel treatment targets. We identify key areas where future research should focus to enable the development of targeted B cell therapies. Frontiers Media S.A. 2021-04-14 /pmc/articles/PMC8079753/ /pubmed/33936097 http://dx.doi.org/10.3389/fimmu.2021.661196 Text en Copyright © 2021 Cargill and Culver 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
Cargill, Tamsin
Culver, Emma L.
The Role of B Cells and B Cell Therapies in Immune-Mediated Liver Diseases
title The Role of B Cells and B Cell Therapies in Immune-Mediated Liver Diseases
title_full The Role of B Cells and B Cell Therapies in Immune-Mediated Liver Diseases
title_fullStr The Role of B Cells and B Cell Therapies in Immune-Mediated Liver Diseases
title_full_unstemmed The Role of B Cells and B Cell Therapies in Immune-Mediated Liver Diseases
title_short The Role of B Cells and B Cell Therapies in Immune-Mediated Liver Diseases
title_sort role of b cells and b cell therapies in immune-mediated liver diseases
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8079753/
https://www.ncbi.nlm.nih.gov/pubmed/33936097
http://dx.doi.org/10.3389/fimmu.2021.661196
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