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Autoimmune Hepatitis: Serum Autoantibodies in Clinical Practice

Circulating autoantibodies are a key diagnostic tool in autoimmune hepatitis (AIH), being positive in 95% of the cases if tested according to dedicated guidelines issued by the International Autoimmune Hepatitis Group. They also allow the distinction between type 1 AIH, characterized by positive ant...

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Autores principales: Terziroli Beretta-Piccoli, Benedetta, Mieli-Vergani, Giorgina, Vergani, Diego
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9464171/
https://www.ncbi.nlm.nih.gov/pubmed/34491531
http://dx.doi.org/10.1007/s12016-021-08888-9
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author Terziroli Beretta-Piccoli, Benedetta
Mieli-Vergani, Giorgina
Vergani, Diego
author_facet Terziroli Beretta-Piccoli, Benedetta
Mieli-Vergani, Giorgina
Vergani, Diego
author_sort Terziroli Beretta-Piccoli, Benedetta
collection PubMed
description Circulating autoantibodies are a key diagnostic tool in autoimmune hepatitis (AIH), being positive in 95% of the cases if tested according to dedicated guidelines issued by the International Autoimmune Hepatitis Group. They also allow the distinction between type 1 AIH, characterized by positive anti-nuclear and/or anti-smooth muscle antibody, and type 2 AIH, characterized by positive anti-liver kidney microsomal type 1 and/or anti-liver cytosol type 1 antibody. Anti-soluble liver antigen is the only AIH-specific autoantibody, and is found in 20–30% of both type 1 and type 2 AIH. Anti-neutrophil cytoplasmic antibody is frequently positive in type 1 AIH, being associated also with inflammatory bowel disease and with primary/autoimmune sclerosing cholangitis. The reference method for autoantibody testing remains indirect immunofluorescence on triple tissue (rodent liver, kidney and stomach), allowing both the detection of the majority of liver-relevant reactivities, including those autoantibodies whose molecular target antigens are unknown. Of note, the current knowledge of the clinical significance of autoantibodies relies on studies based on this technique. However, immunofluorescence requires trained laboratory personnel, is observer-dependent, and lacks standardization, leading to ongoing attempts at replacing this method with automated assays, the sensitivity, and specificity of which, however, require further studies before they can be used as a reliable alternative to immunofluorescence; currently, they may be used as complementary to immunofluorescence.
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spelling pubmed-94641712022-09-12 Autoimmune Hepatitis: Serum Autoantibodies in Clinical Practice Terziroli Beretta-Piccoli, Benedetta Mieli-Vergani, Giorgina Vergani, Diego Clin Rev Allergy Immunol Article Circulating autoantibodies are a key diagnostic tool in autoimmune hepatitis (AIH), being positive in 95% of the cases if tested according to dedicated guidelines issued by the International Autoimmune Hepatitis Group. They also allow the distinction between type 1 AIH, characterized by positive anti-nuclear and/or anti-smooth muscle antibody, and type 2 AIH, characterized by positive anti-liver kidney microsomal type 1 and/or anti-liver cytosol type 1 antibody. Anti-soluble liver antigen is the only AIH-specific autoantibody, and is found in 20–30% of both type 1 and type 2 AIH. Anti-neutrophil cytoplasmic antibody is frequently positive in type 1 AIH, being associated also with inflammatory bowel disease and with primary/autoimmune sclerosing cholangitis. The reference method for autoantibody testing remains indirect immunofluorescence on triple tissue (rodent liver, kidney and stomach), allowing both the detection of the majority of liver-relevant reactivities, including those autoantibodies whose molecular target antigens are unknown. Of note, the current knowledge of the clinical significance of autoantibodies relies on studies based on this technique. However, immunofluorescence requires trained laboratory personnel, is observer-dependent, and lacks standardization, leading to ongoing attempts at replacing this method with automated assays, the sensitivity, and specificity of which, however, require further studies before they can be used as a reliable alternative to immunofluorescence; currently, they may be used as complementary to immunofluorescence. Springer US 2021-09-07 2022 /pmc/articles/PMC9464171/ /pubmed/34491531 http://dx.doi.org/10.1007/s12016-021-08888-9 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Terziroli Beretta-Piccoli, Benedetta
Mieli-Vergani, Giorgina
Vergani, Diego
Autoimmune Hepatitis: Serum Autoantibodies in Clinical Practice
title Autoimmune Hepatitis: Serum Autoantibodies in Clinical Practice
title_full Autoimmune Hepatitis: Serum Autoantibodies in Clinical Practice
title_fullStr Autoimmune Hepatitis: Serum Autoantibodies in Clinical Practice
title_full_unstemmed Autoimmune Hepatitis: Serum Autoantibodies in Clinical Practice
title_short Autoimmune Hepatitis: Serum Autoantibodies in Clinical Practice
title_sort autoimmune hepatitis: serum autoantibodies in clinical practice
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9464171/
https://www.ncbi.nlm.nih.gov/pubmed/34491531
http://dx.doi.org/10.1007/s12016-021-08888-9
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