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Human inborn errors of immunity associated with IRF4

The transcription factor interferon regulatory factor 4 (IRF4) belongs to the IRF family and has several important functions for the adaptive immune response. Mutations affecting IRF family members IRF1, IRF3, IRF7, IRF8, or IRF9 have been described in patients presenting with inborn errors of immun...

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Autores principales: Thouenon, Romane, Kracker, Sven
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10556498/
https://www.ncbi.nlm.nih.gov/pubmed/37809068
http://dx.doi.org/10.3389/fimmu.2023.1236889
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author Thouenon, Romane
Kracker, Sven
author_facet Thouenon, Romane
Kracker, Sven
author_sort Thouenon, Romane
collection PubMed
description The transcription factor interferon regulatory factor 4 (IRF4) belongs to the IRF family and has several important functions for the adaptive immune response. Mutations affecting IRF family members IRF1, IRF3, IRF7, IRF8, or IRF9 have been described in patients presenting with inborn errors of immunity (IEI) highlighting the importance of these factors for the cellular host defense against mycobacterial and/or viral infections. IRF4 deficiency and haploinsufficiency have been associated with IEI. More recently, two novel IRF4 disease-causing mechanisms have been described due to the characterization of IEI patients presenting with cellular immunodeficiency associated with agammaglobulinemia. Here, we review the phenotypes and physiopathological mechanisms underlying IEI of IRF family members and, in particular, IRF4.
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spelling pubmed-105564982023-10-07 Human inborn errors of immunity associated with IRF4 Thouenon, Romane Kracker, Sven Front Immunol Immunology The transcription factor interferon regulatory factor 4 (IRF4) belongs to the IRF family and has several important functions for the adaptive immune response. Mutations affecting IRF family members IRF1, IRF3, IRF7, IRF8, or IRF9 have been described in patients presenting with inborn errors of immunity (IEI) highlighting the importance of these factors for the cellular host defense against mycobacterial and/or viral infections. IRF4 deficiency and haploinsufficiency have been associated with IEI. More recently, two novel IRF4 disease-causing mechanisms have been described due to the characterization of IEI patients presenting with cellular immunodeficiency associated with agammaglobulinemia. Here, we review the phenotypes and physiopathological mechanisms underlying IEI of IRF family members and, in particular, IRF4. Frontiers Media S.A. 2023-09-22 /pmc/articles/PMC10556498/ /pubmed/37809068 http://dx.doi.org/10.3389/fimmu.2023.1236889 Text en Copyright © 2023 Thouenon and Kracker 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
Thouenon, Romane
Kracker, Sven
Human inborn errors of immunity associated with IRF4
title Human inborn errors of immunity associated with IRF4
title_full Human inborn errors of immunity associated with IRF4
title_fullStr Human inborn errors of immunity associated with IRF4
title_full_unstemmed Human inborn errors of immunity associated with IRF4
title_short Human inborn errors of immunity associated with IRF4
title_sort human inborn errors of immunity associated with irf4
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10556498/
https://www.ncbi.nlm.nih.gov/pubmed/37809068
http://dx.doi.org/10.3389/fimmu.2023.1236889
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