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Role of the CXCL13/CXCR5 Axis in Autoimmune Diseases

CXCL13 is a B-cell chemokine produced mainly by mesenchymal lymphoid tissue organizer cells, follicular dendritic cells, and human T follicular helper cells. By binding to its receptor, CXCR5, CXCL13 plays an important role in lymphoid neogenesis, lymphoid organization, and immune responses. Recent...

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Detalles Bibliográficos
Autores principales: Pan, Zijian, Zhu, Tong, Liu, Yanjun, Zhang, Nannan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8931035/
https://www.ncbi.nlm.nih.gov/pubmed/35309354
http://dx.doi.org/10.3389/fimmu.2022.850998
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author Pan, Zijian
Zhu, Tong
Liu, Yanjun
Zhang, Nannan
author_facet Pan, Zijian
Zhu, Tong
Liu, Yanjun
Zhang, Nannan
author_sort Pan, Zijian
collection PubMed
description CXCL13 is a B-cell chemokine produced mainly by mesenchymal lymphoid tissue organizer cells, follicular dendritic cells, and human T follicular helper cells. By binding to its receptor, CXCR5, CXCL13 plays an important role in lymphoid neogenesis, lymphoid organization, and immune responses. Recent studies have found that CXCL13 and its receptor CXCR5 are implicated in the pathogenesis of several autoimmune diseases, such as rheumatoid arthritis, multiple sclerosis, systemic lupus erythematosus, primary Sjögren’s syndrome, myasthenia gravis, and inflammatory bowel disease. In this review, we discuss the biological features of CXCL13 and CXCR5 and the recent findings on the pathogenic roles of the CXCL13/CXCR5 axis in autoimmune diseases. Furthermore, we discuss the potential role of CXCL13 as a disease biomarker and therapeutic target in autoimmune diseases.
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spelling pubmed-89310352022-03-19 Role of the CXCL13/CXCR5 Axis in Autoimmune Diseases Pan, Zijian Zhu, Tong Liu, Yanjun Zhang, Nannan Front Immunol Immunology CXCL13 is a B-cell chemokine produced mainly by mesenchymal lymphoid tissue organizer cells, follicular dendritic cells, and human T follicular helper cells. By binding to its receptor, CXCR5, CXCL13 plays an important role in lymphoid neogenesis, lymphoid organization, and immune responses. Recent studies have found that CXCL13 and its receptor CXCR5 are implicated in the pathogenesis of several autoimmune diseases, such as rheumatoid arthritis, multiple sclerosis, systemic lupus erythematosus, primary Sjögren’s syndrome, myasthenia gravis, and inflammatory bowel disease. In this review, we discuss the biological features of CXCL13 and CXCR5 and the recent findings on the pathogenic roles of the CXCL13/CXCR5 axis in autoimmune diseases. Furthermore, we discuss the potential role of CXCL13 as a disease biomarker and therapeutic target in autoimmune diseases. Frontiers Media S.A. 2022-03-04 /pmc/articles/PMC8931035/ /pubmed/35309354 http://dx.doi.org/10.3389/fimmu.2022.850998 Text en Copyright © 2022 Pan, Zhu, Liu and Zhang 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
Pan, Zijian
Zhu, Tong
Liu, Yanjun
Zhang, Nannan
Role of the CXCL13/CXCR5 Axis in Autoimmune Diseases
title Role of the CXCL13/CXCR5 Axis in Autoimmune Diseases
title_full Role of the CXCL13/CXCR5 Axis in Autoimmune Diseases
title_fullStr Role of the CXCL13/CXCR5 Axis in Autoimmune Diseases
title_full_unstemmed Role of the CXCL13/CXCR5 Axis in Autoimmune Diseases
title_short Role of the CXCL13/CXCR5 Axis in Autoimmune Diseases
title_sort role of the cxcl13/cxcr5 axis in autoimmune diseases
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8931035/
https://www.ncbi.nlm.nih.gov/pubmed/35309354
http://dx.doi.org/10.3389/fimmu.2022.850998
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