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Asialoglycoprotein receptor (ASGPR): a peculiar target of liver-specific autoimmunity

Asialoglycoprotein receptor (ASGPR) autoantibodies have been considered specific markers of autoimmune hepatitis (AIH). The exact mechanisms responsible for the development of these autoantibodies and leading to autoimmunity to this peculiar liver receptor remain elusive. Furthermore, loss of T cell...

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Detalles Bibliográficos
Autores principales: Roggenbuck, Dirk, Mytilinaiou, Maria G., Lapin, Sergey V., Reinhold, Dirk, Conrad, Karsten
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer International Publishing 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4389076/
https://www.ncbi.nlm.nih.gov/pubmed/26000135
http://dx.doi.org/10.1007/s13317-012-0041-4
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author Roggenbuck, Dirk
Mytilinaiou, Maria G.
Lapin, Sergey V.
Reinhold, Dirk
Conrad, Karsten
author_facet Roggenbuck, Dirk
Mytilinaiou, Maria G.
Lapin, Sergey V.
Reinhold, Dirk
Conrad, Karsten
author_sort Roggenbuck, Dirk
collection PubMed
description Asialoglycoprotein receptor (ASGPR) autoantibodies have been considered specific markers of autoimmune hepatitis (AIH). The exact mechanisms responsible for the development of these autoantibodies and leading to autoimmunity to this peculiar liver receptor remain elusive. Furthermore, loss of T cell tolerance to ASGPR has been demonstrated in patients with AIH, but it is poorly understood whether such liver-specific T cell responses bear a pathogenic potential and/or participate in the precipitation of AIH. Newly developed enzyme-linked immunosorbent assays have led to the investigation of the sensitivity and specificity of anti-ASGPR antibodies for AIH. The present review provides an overview of the diagnostic and clinical relevance of anti-ASGPR antibodies. A thorough investigation of the autoreactivity against ASGPR may assist efforts to understand liver autoimmunity in susceptible individuals.
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spelling pubmed-43890762015-05-21 Asialoglycoprotein receptor (ASGPR): a peculiar target of liver-specific autoimmunity Roggenbuck, Dirk Mytilinaiou, Maria G. Lapin, Sergey V. Reinhold, Dirk Conrad, Karsten Auto Immun Highlights Review Article Asialoglycoprotein receptor (ASGPR) autoantibodies have been considered specific markers of autoimmune hepatitis (AIH). The exact mechanisms responsible for the development of these autoantibodies and leading to autoimmunity to this peculiar liver receptor remain elusive. Furthermore, loss of T cell tolerance to ASGPR has been demonstrated in patients with AIH, but it is poorly understood whether such liver-specific T cell responses bear a pathogenic potential and/or participate in the precipitation of AIH. Newly developed enzyme-linked immunosorbent assays have led to the investigation of the sensitivity and specificity of anti-ASGPR antibodies for AIH. The present review provides an overview of the diagnostic and clinical relevance of anti-ASGPR antibodies. A thorough investigation of the autoreactivity against ASGPR may assist efforts to understand liver autoimmunity in susceptible individuals. Springer International Publishing 2012-10-30 /pmc/articles/PMC4389076/ /pubmed/26000135 http://dx.doi.org/10.1007/s13317-012-0041-4 Text en © Springer-Verlag Italia 2012
spellingShingle Review Article
Roggenbuck, Dirk
Mytilinaiou, Maria G.
Lapin, Sergey V.
Reinhold, Dirk
Conrad, Karsten
Asialoglycoprotein receptor (ASGPR): a peculiar target of liver-specific autoimmunity
title Asialoglycoprotein receptor (ASGPR): a peculiar target of liver-specific autoimmunity
title_full Asialoglycoprotein receptor (ASGPR): a peculiar target of liver-specific autoimmunity
title_fullStr Asialoglycoprotein receptor (ASGPR): a peculiar target of liver-specific autoimmunity
title_full_unstemmed Asialoglycoprotein receptor (ASGPR): a peculiar target of liver-specific autoimmunity
title_short Asialoglycoprotein receptor (ASGPR): a peculiar target of liver-specific autoimmunity
title_sort asialoglycoprotein receptor (asgpr): a peculiar target of liver-specific autoimmunity
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4389076/
https://www.ncbi.nlm.nih.gov/pubmed/26000135
http://dx.doi.org/10.1007/s13317-012-0041-4
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