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The link between rheumatic disorders and inborn errors of immunity

Inborn errors of immunity (IEIs) are immunological disorders characterized by variable susceptibility to infections, immune dysregulation and/or malignancies, as a consequence of damaging germline variants in single genes. Though initially identified among patients with unusual, severe or recurrent...

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Detalles Bibliográficos
Autores principales: Sogkas, Georgios, Witte, Torsten
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9996386/
https://www.ncbi.nlm.nih.gov/pubmed/36870198
http://dx.doi.org/10.1016/j.ebiom.2023.104501
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author Sogkas, Georgios
Witte, Torsten
author_facet Sogkas, Georgios
Witte, Torsten
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description Inborn errors of immunity (IEIs) are immunological disorders characterized by variable susceptibility to infections, immune dysregulation and/or malignancies, as a consequence of damaging germline variants in single genes. Though initially identified among patients with unusual, severe or recurrent infections, non-infectious manifestations and especially immune dysregulation in the form of autoimmunity or autoinflammation can be the first or dominant phenotypic aspect of IEIs. An increasing number of IEIs causing autoimmunity or autoinflammation, including rheumatic disease have been reported over the last decade. Despite their rarity, identification of those disorders provided insight into the pathomechanisms of immune dysregulation, which may be relevant for understanding the pathogenesis of systemic rheumatic disorders. In this review, we present novel IEIs primarily causing autoimmunity or autoinflammation along with their pathogenic mechanisms. In addition, we explore the likely pathophysiological and clinical relevance of IEIs in systemic rheumatic disorders.
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spelling pubmed-99963862023-03-10 The link between rheumatic disorders and inborn errors of immunity Sogkas, Georgios Witte, Torsten eBioMedicine Review Inborn errors of immunity (IEIs) are immunological disorders characterized by variable susceptibility to infections, immune dysregulation and/or malignancies, as a consequence of damaging germline variants in single genes. Though initially identified among patients with unusual, severe or recurrent infections, non-infectious manifestations and especially immune dysregulation in the form of autoimmunity or autoinflammation can be the first or dominant phenotypic aspect of IEIs. An increasing number of IEIs causing autoimmunity or autoinflammation, including rheumatic disease have been reported over the last decade. Despite their rarity, identification of those disorders provided insight into the pathomechanisms of immune dysregulation, which may be relevant for understanding the pathogenesis of systemic rheumatic disorders. In this review, we present novel IEIs primarily causing autoimmunity or autoinflammation along with their pathogenic mechanisms. In addition, we explore the likely pathophysiological and clinical relevance of IEIs in systemic rheumatic disorders. Elsevier 2023-03-02 /pmc/articles/PMC9996386/ /pubmed/36870198 http://dx.doi.org/10.1016/j.ebiom.2023.104501 Text en © 2023 The Author(s) https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Sogkas, Georgios
Witte, Torsten
The link between rheumatic disorders and inborn errors of immunity
title The link between rheumatic disorders and inborn errors of immunity
title_full The link between rheumatic disorders and inborn errors of immunity
title_fullStr The link between rheumatic disorders and inborn errors of immunity
title_full_unstemmed The link between rheumatic disorders and inborn errors of immunity
title_short The link between rheumatic disorders and inborn errors of immunity
title_sort link between rheumatic disorders and inborn errors of immunity
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9996386/
https://www.ncbi.nlm.nih.gov/pubmed/36870198
http://dx.doi.org/10.1016/j.ebiom.2023.104501
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