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B Cell Immunity in Lung Transplant Rejection - Effector Mechanisms and Therapeutic Implications

Allograft rejection remains the major hurdle in lung transplantation despite modern immunosuppressive treatment. As part of the alloreactive process, B cells are increasingly recognized as modulators of alloimmunity and initiators of a donor-specific humoral response. In chronically rejected lung al...

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Detalles Bibliográficos
Autores principales: Ohm, Birte, Jungraithmayr, Wolfgang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8934882/
https://www.ncbi.nlm.nih.gov/pubmed/35320934
http://dx.doi.org/10.3389/fimmu.2022.845867
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author Ohm, Birte
Jungraithmayr, Wolfgang
author_facet Ohm, Birte
Jungraithmayr, Wolfgang
author_sort Ohm, Birte
collection PubMed
description Allograft rejection remains the major hurdle in lung transplantation despite modern immunosuppressive treatment. As part of the alloreactive process, B cells are increasingly recognized as modulators of alloimmunity and initiators of a donor-specific humoral response. In chronically rejected lung allografts, B cells contribute to the formation of tertiary lymphoid structures and promote local alloimmune responses. However, B cells are functionally heterogeneous and some B cell subsets may promote alloimmune tolerance. In this review, we describe the current understanding of B-cell-dependent mechanisms in pulmonary allograft rejection and highlight promising future strategies that employ B cell-targeted therapies.
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spelling pubmed-89348822022-03-22 B Cell Immunity in Lung Transplant Rejection - Effector Mechanisms and Therapeutic Implications Ohm, Birte Jungraithmayr, Wolfgang Front Immunol Immunology Allograft rejection remains the major hurdle in lung transplantation despite modern immunosuppressive treatment. As part of the alloreactive process, B cells are increasingly recognized as modulators of alloimmunity and initiators of a donor-specific humoral response. In chronically rejected lung allografts, B cells contribute to the formation of tertiary lymphoid structures and promote local alloimmune responses. However, B cells are functionally heterogeneous and some B cell subsets may promote alloimmune tolerance. In this review, we describe the current understanding of B-cell-dependent mechanisms in pulmonary allograft rejection and highlight promising future strategies that employ B cell-targeted therapies. Frontiers Media S.A. 2022-03-07 /pmc/articles/PMC8934882/ /pubmed/35320934 http://dx.doi.org/10.3389/fimmu.2022.845867 Text en Copyright © 2022 Ohm and Jungraithmayr 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
Ohm, Birte
Jungraithmayr, Wolfgang
B Cell Immunity in Lung Transplant Rejection - Effector Mechanisms and Therapeutic Implications
title B Cell Immunity in Lung Transplant Rejection - Effector Mechanisms and Therapeutic Implications
title_full B Cell Immunity in Lung Transplant Rejection - Effector Mechanisms and Therapeutic Implications
title_fullStr B Cell Immunity in Lung Transplant Rejection - Effector Mechanisms and Therapeutic Implications
title_full_unstemmed B Cell Immunity in Lung Transplant Rejection - Effector Mechanisms and Therapeutic Implications
title_short B Cell Immunity in Lung Transplant Rejection - Effector Mechanisms and Therapeutic Implications
title_sort b cell immunity in lung transplant rejection - effector mechanisms and therapeutic implications
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8934882/
https://www.ncbi.nlm.nih.gov/pubmed/35320934
http://dx.doi.org/10.3389/fimmu.2022.845867
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