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Interferon Alpha in Systemic Lupus Erythematosus

The pleiotropic cytokine interferon alpha is involved in multiple aspects of lupus etiology and pathogenesis. Interferon alpha is important under normal circumstances for antiviral responses and immune activation. However, heightened levels of serum interferon alpha and expression of interferon resp...

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Detalles Bibliográficos
Autores principales: Niewold, Timothy B., Clark, Daniel N., Salloum, Rafah, Poole, Brian D.
Formato: Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2896914/
https://www.ncbi.nlm.nih.gov/pubmed/20652065
http://dx.doi.org/10.1155/2010/948364
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author Niewold, Timothy B.
Clark, Daniel N.
Salloum, Rafah
Poole, Brian D.
author_facet Niewold, Timothy B.
Clark, Daniel N.
Salloum, Rafah
Poole, Brian D.
author_sort Niewold, Timothy B.
collection PubMed
description The pleiotropic cytokine interferon alpha is involved in multiple aspects of lupus etiology and pathogenesis. Interferon alpha is important under normal circumstances for antiviral responses and immune activation. However, heightened levels of serum interferon alpha and expression of interferon response genes are common in lupus patients. Lupus-associated autoantibodies can drive the production of interferon alpha and heightened levels of interferon interfere with immune regulation. Several genes in the pathways leading to interferon production or signaling are associated with risk for lupus. Clinical and cellular manifestations of excess interferon alpha in lupus combined with the genetic risk factors associated with interferon make this cytokine a rare bridge between genetic risk and phenotypic effects. Interferon alpha influences the clinical picture of lupus and may represent a therapeutic target. This paper provides an overview of the cellular, genetic, and clinical aspects of interferon alpha in lupus.
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spelling pubmed-28969142010-07-22 Interferon Alpha in Systemic Lupus Erythematosus Niewold, Timothy B. Clark, Daniel N. Salloum, Rafah Poole, Brian D. J Biomed Biotechnol Review Article The pleiotropic cytokine interferon alpha is involved in multiple aspects of lupus etiology and pathogenesis. Interferon alpha is important under normal circumstances for antiviral responses and immune activation. However, heightened levels of serum interferon alpha and expression of interferon response genes are common in lupus patients. Lupus-associated autoantibodies can drive the production of interferon alpha and heightened levels of interferon interfere with immune regulation. Several genes in the pathways leading to interferon production or signaling are associated with risk for lupus. Clinical and cellular manifestations of excess interferon alpha in lupus combined with the genetic risk factors associated with interferon make this cytokine a rare bridge between genetic risk and phenotypic effects. Interferon alpha influences the clinical picture of lupus and may represent a therapeutic target. This paper provides an overview of the cellular, genetic, and clinical aspects of interferon alpha in lupus. Hindawi Publishing Corporation 2010 2010-06-29 /pmc/articles/PMC2896914/ /pubmed/20652065 http://dx.doi.org/10.1155/2010/948364 Text en Copyright © 2010 Timothy B. Niewold et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review Article
Niewold, Timothy B.
Clark, Daniel N.
Salloum, Rafah
Poole, Brian D.
Interferon Alpha in Systemic Lupus Erythematosus
title Interferon Alpha in Systemic Lupus Erythematosus
title_full Interferon Alpha in Systemic Lupus Erythematosus
title_fullStr Interferon Alpha in Systemic Lupus Erythematosus
title_full_unstemmed Interferon Alpha in Systemic Lupus Erythematosus
title_short Interferon Alpha in Systemic Lupus Erythematosus
title_sort interferon alpha in systemic lupus erythematosus
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2896914/
https://www.ncbi.nlm.nih.gov/pubmed/20652065
http://dx.doi.org/10.1155/2010/948364
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