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Germline STAT3 gain-of-function mutations in primary immunodeficiency: Impact on the cellular and clinical phenotype

Signal transducer and activator of transcription 3 (STAT3) is a key transcription factor involved in regulation of immune cell activation and differentiation. Recent discoveries highlight the role of germline activating STAT3 mutations in inborn errors of immunity characterized by early-onset multi-...

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Detalles Bibliográficos
Autores principales: Faletti, Laura, Ehl, Stephan, Heeg, Maximilian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Chang Gung University 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8514798/
https://www.ncbi.nlm.nih.gov/pubmed/34366294
http://dx.doi.org/10.1016/j.bj.2021.03.003
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author Faletti, Laura
Ehl, Stephan
Heeg, Maximilian
author_facet Faletti, Laura
Ehl, Stephan
Heeg, Maximilian
author_sort Faletti, Laura
collection PubMed
description Signal transducer and activator of transcription 3 (STAT3) is a key transcription factor involved in regulation of immune cell activation and differentiation. Recent discoveries highlight the role of germline activating STAT3 mutations in inborn errors of immunity characterized by early-onset multi-organ autoimmunity and lymphoproliferation. Much progress has been made in defining the clinical spectrum of STAT3 GOF disease and unraveling the molecular and cellular mechanisms underlying this disease. In this review, we summarize our current understanding of the disease and discuss the clinical phenotype, diagnostic approach, cellular and molecular effects of STAT3 GOF mutations and therapeutic concepts for these patients.
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spelling pubmed-85147982021-10-21 Germline STAT3 gain-of-function mutations in primary immunodeficiency: Impact on the cellular and clinical phenotype Faletti, Laura Ehl, Stephan Heeg, Maximilian Biomed J Review Article: Special Edition Signal transducer and activator of transcription 3 (STAT3) is a key transcription factor involved in regulation of immune cell activation and differentiation. Recent discoveries highlight the role of germline activating STAT3 mutations in inborn errors of immunity characterized by early-onset multi-organ autoimmunity and lymphoproliferation. Much progress has been made in defining the clinical spectrum of STAT3 GOF disease and unraveling the molecular and cellular mechanisms underlying this disease. In this review, we summarize our current understanding of the disease and discuss the clinical phenotype, diagnostic approach, cellular and molecular effects of STAT3 GOF mutations and therapeutic concepts for these patients. Chang Gung University 2021-08 2021-03-20 /pmc/articles/PMC8514798/ /pubmed/34366294 http://dx.doi.org/10.1016/j.bj.2021.03.003 Text en © 2021 Chang Gung University. Publishing services provided by Elsevier B.V. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Review Article: Special Edition
Faletti, Laura
Ehl, Stephan
Heeg, Maximilian
Germline STAT3 gain-of-function mutations in primary immunodeficiency: Impact on the cellular and clinical phenotype
title Germline STAT3 gain-of-function mutations in primary immunodeficiency: Impact on the cellular and clinical phenotype
title_full Germline STAT3 gain-of-function mutations in primary immunodeficiency: Impact on the cellular and clinical phenotype
title_fullStr Germline STAT3 gain-of-function mutations in primary immunodeficiency: Impact on the cellular and clinical phenotype
title_full_unstemmed Germline STAT3 gain-of-function mutations in primary immunodeficiency: Impact on the cellular and clinical phenotype
title_short Germline STAT3 gain-of-function mutations in primary immunodeficiency: Impact on the cellular and clinical phenotype
title_sort germline stat3 gain-of-function mutations in primary immunodeficiency: impact on the cellular and clinical phenotype
topic Review Article: Special Edition
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8514798/
https://www.ncbi.nlm.nih.gov/pubmed/34366294
http://dx.doi.org/10.1016/j.bj.2021.03.003
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