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Pathogenicity of Misfolded and Dimeric HLA-B27 Molecules

The association between HLA-B27 and the group of autoimmune inflammatory arthritic diseases, the spondyloarthropathies (SpAs) which include ankylosing spondylitis (AS) and Reactive Arthritis (ReA), has been well established and remains the strongest association between any HLA molecule and autoimmun...

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Detalles Bibliográficos
Autores principales: Antoniou, Antony N., Lenart, Izabela, Guiliano, David B.
Formato: Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3087312/
https://www.ncbi.nlm.nih.gov/pubmed/21547037
http://dx.doi.org/10.1155/2011/486856
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author Antoniou, Antony N.
Lenart, Izabela
Guiliano, David B.
author_facet Antoniou, Antony N.
Lenart, Izabela
Guiliano, David B.
author_sort Antoniou, Antony N.
collection PubMed
description The association between HLA-B27 and the group of autoimmune inflammatory arthritic diseases, the spondyloarthropathies (SpAs) which include ankylosing spondylitis (AS) and Reactive Arthritis (ReA), has been well established and remains the strongest association between any HLA molecule and autoimmune disease. The mechanism behind this striking association remains elusive; however animal model and biochemical data suggest that HLA-B27 misfolding may be key to understanding its association with the SpAs. Recent investigations have focused on the unusual biochemical structures of HLA-B27 and their potential role in SpA pathogenesis. Here we discuss how these unusual biochemical structures may participate in cellular events leading to chronic inflammation and thus disease progression.
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spelling pubmed-30873122011-05-05 Pathogenicity of Misfolded and Dimeric HLA-B27 Molecules Antoniou, Antony N. Lenart, Izabela Guiliano, David B. Int J Rheumatol Review Article The association between HLA-B27 and the group of autoimmune inflammatory arthritic diseases, the spondyloarthropathies (SpAs) which include ankylosing spondylitis (AS) and Reactive Arthritis (ReA), has been well established and remains the strongest association between any HLA molecule and autoimmune disease. The mechanism behind this striking association remains elusive; however animal model and biochemical data suggest that HLA-B27 misfolding may be key to understanding its association with the SpAs. Recent investigations have focused on the unusual biochemical structures of HLA-B27 and their potential role in SpA pathogenesis. Here we discuss how these unusual biochemical structures may participate in cellular events leading to chronic inflammation and thus disease progression. Hindawi Publishing Corporation 2011 2011-03-30 /pmc/articles/PMC3087312/ /pubmed/21547037 http://dx.doi.org/10.1155/2011/486856 Text en Copyright © 2011 Antony N. Antoniou et al. https://creativecommons.org/licenses/by/3.0/ 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
Antoniou, Antony N.
Lenart, Izabela
Guiliano, David B.
Pathogenicity of Misfolded and Dimeric HLA-B27 Molecules
title Pathogenicity of Misfolded and Dimeric HLA-B27 Molecules
title_full Pathogenicity of Misfolded and Dimeric HLA-B27 Molecules
title_fullStr Pathogenicity of Misfolded and Dimeric HLA-B27 Molecules
title_full_unstemmed Pathogenicity of Misfolded and Dimeric HLA-B27 Molecules
title_short Pathogenicity of Misfolded and Dimeric HLA-B27 Molecules
title_sort pathogenicity of misfolded and dimeric hla-b27 molecules
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3087312/
https://www.ncbi.nlm.nih.gov/pubmed/21547037
http://dx.doi.org/10.1155/2011/486856
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