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B-cell response in solid organ transplantation

The transcriptional regulation of B-cell response to antigen stimulation is complex and involves an intricate network of dynamic signals from cytokines and transcription factors propagated from T-cell interaction. Long-term alloimmunity, in the setting of organ transplantation, is dependent on this...

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Detalles Bibliográficos
Autores principales: Yi, Stephanie G., Gaber, Ahmed Osama, Chen, Wenhao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9395675/
https://www.ncbi.nlm.nih.gov/pubmed/36016958
http://dx.doi.org/10.3389/fimmu.2022.895157
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author Yi, Stephanie G.
Gaber, Ahmed Osama
Chen, Wenhao
author_facet Yi, Stephanie G.
Gaber, Ahmed Osama
Chen, Wenhao
author_sort Yi, Stephanie G.
collection PubMed
description The transcriptional regulation of B-cell response to antigen stimulation is complex and involves an intricate network of dynamic signals from cytokines and transcription factors propagated from T-cell interaction. Long-term alloimmunity, in the setting of organ transplantation, is dependent on this B-cell response, which does not appear to be halted by current immunosuppressive regimens which are targeted at T cells. There is emerging evidence that shows that B cells have a diverse response to solid organ transplantation that extends beyond plasma cell antibody production. In this review, we discuss the mechanistic pathways of B-cell activation and differentiation as they relate to the transcriptional regulation of germinal center B cells, plasma cells, and memory B cells in the setting of solid organ transplantation.
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spelling pubmed-93956752022-08-24 B-cell response in solid organ transplantation Yi, Stephanie G. Gaber, Ahmed Osama Chen, Wenhao Front Immunol Immunology The transcriptional regulation of B-cell response to antigen stimulation is complex and involves an intricate network of dynamic signals from cytokines and transcription factors propagated from T-cell interaction. Long-term alloimmunity, in the setting of organ transplantation, is dependent on this B-cell response, which does not appear to be halted by current immunosuppressive regimens which are targeted at T cells. There is emerging evidence that shows that B cells have a diverse response to solid organ transplantation that extends beyond plasma cell antibody production. In this review, we discuss the mechanistic pathways of B-cell activation and differentiation as they relate to the transcriptional regulation of germinal center B cells, plasma cells, and memory B cells in the setting of solid organ transplantation. Frontiers Media S.A. 2022-08-09 /pmc/articles/PMC9395675/ /pubmed/36016958 http://dx.doi.org/10.3389/fimmu.2022.895157 Text en Copyright © 2022 Yi, Gaber and Chen 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
Yi, Stephanie G.
Gaber, Ahmed Osama
Chen, Wenhao
B-cell response in solid organ transplantation
title B-cell response in solid organ transplantation
title_full B-cell response in solid organ transplantation
title_fullStr B-cell response in solid organ transplantation
title_full_unstemmed B-cell response in solid organ transplantation
title_short B-cell response in solid organ transplantation
title_sort b-cell response in solid organ transplantation
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9395675/
https://www.ncbi.nlm.nih.gov/pubmed/36016958
http://dx.doi.org/10.3389/fimmu.2022.895157
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