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Psoriatic arthritis: from pathogenesis to therapy

Psoriatic arthritis is a multigenic autoimmune disease that involves synovial tissue, entheseal sites and skin, and that may result in significant joint damage. Although there are no diagnostic tests for psoriatic arthritis, research has identified consistent features that help to distinguish the co...

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Detalles Bibliográficos
Autores principales: FitzGerald, Oliver, Winchester, Robert
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2688229/
https://www.ncbi.nlm.nih.gov/pubmed/19232079
http://dx.doi.org/10.1186/ar2580
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author FitzGerald, Oliver
Winchester, Robert
author_facet FitzGerald, Oliver
Winchester, Robert
author_sort FitzGerald, Oliver
collection PubMed
description Psoriatic arthritis is a multigenic autoimmune disease that involves synovial tissue, entheseal sites and skin, and that may result in significant joint damage. Although there are no diagnostic tests for psoriatic arthritis, research has identified consistent features that help to distinguish the condition from other common rheumatic diseases. Comparison of HLA-B and HLA-C regions in psoriatic arthritis with those in psoriasis without joint involvement demonstrates significant differences, such that psoriatic arthritis cannot be viewed simply as a subset of genetically homogeneous psoriasis. T-cell receptor phenotypic studies have failed to identify antigen-driven clones, and an alternative hypothesis for CD8 stimulation involving innate immune signals is proposed. Finally, imaging studies have highlighted entheseal involvement in psoriatic arthritis, and it is possible that entheseal-derived antigens may trigger an immune response that is critically involved in disease pathogenesis.
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spelling pubmed-26882292009-08-12 Psoriatic arthritis: from pathogenesis to therapy FitzGerald, Oliver Winchester, Robert Arthritis Res Ther Review Psoriatic arthritis is a multigenic autoimmune disease that involves synovial tissue, entheseal sites and skin, and that may result in significant joint damage. Although there are no diagnostic tests for psoriatic arthritis, research has identified consistent features that help to distinguish the condition from other common rheumatic diseases. Comparison of HLA-B and HLA-C regions in psoriatic arthritis with those in psoriasis without joint involvement demonstrates significant differences, such that psoriatic arthritis cannot be viewed simply as a subset of genetically homogeneous psoriasis. T-cell receptor phenotypic studies have failed to identify antigen-driven clones, and an alternative hypothesis for CD8 stimulation involving innate immune signals is proposed. Finally, imaging studies have highlighted entheseal involvement in psoriatic arthritis, and it is possible that entheseal-derived antigens may trigger an immune response that is critically involved in disease pathogenesis. BioMed Central 2009 2009-02-12 /pmc/articles/PMC2688229/ /pubmed/19232079 http://dx.doi.org/10.1186/ar2580 Text en Copyright © 2009 BioMed Central Ltd
spellingShingle Review
FitzGerald, Oliver
Winchester, Robert
Psoriatic arthritis: from pathogenesis to therapy
title Psoriatic arthritis: from pathogenesis to therapy
title_full Psoriatic arthritis: from pathogenesis to therapy
title_fullStr Psoriatic arthritis: from pathogenesis to therapy
title_full_unstemmed Psoriatic arthritis: from pathogenesis to therapy
title_short Psoriatic arthritis: from pathogenesis to therapy
title_sort psoriatic arthritis: from pathogenesis to therapy
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2688229/
https://www.ncbi.nlm.nih.gov/pubmed/19232079
http://dx.doi.org/10.1186/ar2580
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