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Autoantibody profiles in autoimmune hepatitis and chronic hepatitis C identifies similarities in patients with severe disease

AIM: To determine how the auto-antibodies (Abs) profiles overlap in chronic hepatitis C infection (CHC) and autoimmune hepatitis (AIH) and correlate to liver disease. METHODS: Levels of antinuclear Ab, smooth muscle antibody (SMA) and liver/kidney microsomal-1 (LKM-1) Ab and markers of liver damage...

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Autores principales: Amin, Kawa, Rasool, Aram H, Hattem, Ali, Al-Karboly, Taha AM, Taher, Taher E, Bystrom, Jonas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Baishideng Publishing Group Inc 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5330819/
https://www.ncbi.nlm.nih.gov/pubmed/28293081
http://dx.doi.org/10.3748/wjg.v23.i8.1345
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author Amin, Kawa
Rasool, Aram H
Hattem, Ali
Al-Karboly, Taha AM
Taher, Taher E
Bystrom, Jonas
author_facet Amin, Kawa
Rasool, Aram H
Hattem, Ali
Al-Karboly, Taha AM
Taher, Taher E
Bystrom, Jonas
author_sort Amin, Kawa
collection PubMed
description AIM: To determine how the auto-antibodies (Abs) profiles overlap in chronic hepatitis C infection (CHC) and autoimmune hepatitis (AIH) and correlate to liver disease. METHODS: Levels of antinuclear Ab, smooth muscle antibody (SMA) and liver/kidney microsomal-1 (LKM-1) Ab and markers of liver damage were determined in the sera of 50 patients with CHC infection, 20 AIH patients and 20 healthy controls using enzyme linked immunosorbent assay and other immune assays. RESULTS: We found that AIH patients had more severe liver disease as determined by elevation of total IgG, alkaline phosphatase, total serum bilirubin and serum transaminases and significantly higher prevalence of the three non-organ-specific autoantibodies (auto-Abs) than CHC patients. Antinuclear Ab, SMA and LKM-1 Ab were also present in 36% of CHC patients and related to disease severity. CHC cases positive for auto-Abs were directly comparable to AIH in respect of most markers of liver damage and total IgG. These cases had longer disease duration compared with auto-Ab negative cases, but there was no difference in gender, age or viral load. KLM-1(+) Ab CHC cases showed best overlap with AIH. CONCLUSION: Auto-Ab levels in CHC may be important markers of disease severity and positive cases have a disease similar to AIH. Auto-Abs might have a pathogenic role as indicated by elevated markers of liver damage. Future studies will unravel any novel associations between these two diseases, whether genetic or other.
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spelling pubmed-53308192017-03-14 Autoantibody profiles in autoimmune hepatitis and chronic hepatitis C identifies similarities in patients with severe disease Amin, Kawa Rasool, Aram H Hattem, Ali Al-Karboly, Taha AM Taher, Taher E Bystrom, Jonas World J Gastroenterol Basic Study AIM: To determine how the auto-antibodies (Abs) profiles overlap in chronic hepatitis C infection (CHC) and autoimmune hepatitis (AIH) and correlate to liver disease. METHODS: Levels of antinuclear Ab, smooth muscle antibody (SMA) and liver/kidney microsomal-1 (LKM-1) Ab and markers of liver damage were determined in the sera of 50 patients with CHC infection, 20 AIH patients and 20 healthy controls using enzyme linked immunosorbent assay and other immune assays. RESULTS: We found that AIH patients had more severe liver disease as determined by elevation of total IgG, alkaline phosphatase, total serum bilirubin and serum transaminases and significantly higher prevalence of the three non-organ-specific autoantibodies (auto-Abs) than CHC patients. Antinuclear Ab, SMA and LKM-1 Ab were also present in 36% of CHC patients and related to disease severity. CHC cases positive for auto-Abs were directly comparable to AIH in respect of most markers of liver damage and total IgG. These cases had longer disease duration compared with auto-Ab negative cases, but there was no difference in gender, age or viral load. KLM-1(+) Ab CHC cases showed best overlap with AIH. CONCLUSION: Auto-Ab levels in CHC may be important markers of disease severity and positive cases have a disease similar to AIH. Auto-Abs might have a pathogenic role as indicated by elevated markers of liver damage. Future studies will unravel any novel associations between these two diseases, whether genetic or other. Baishideng Publishing Group Inc 2017-02-28 2017-02-28 /pmc/articles/PMC5330819/ /pubmed/28293081 http://dx.doi.org/10.3748/wjg.v23.i8.1345 Text en ©The Author(s) 2017. Published by Baishideng Publishing Group Inc. All rights reserved. http://creativecommons.org/licenses/by-nc/4.0/ This article is an open-access article which was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial.
spellingShingle Basic Study
Amin, Kawa
Rasool, Aram H
Hattem, Ali
Al-Karboly, Taha AM
Taher, Taher E
Bystrom, Jonas
Autoantibody profiles in autoimmune hepatitis and chronic hepatitis C identifies similarities in patients with severe disease
title Autoantibody profiles in autoimmune hepatitis and chronic hepatitis C identifies similarities in patients with severe disease
title_full Autoantibody profiles in autoimmune hepatitis and chronic hepatitis C identifies similarities in patients with severe disease
title_fullStr Autoantibody profiles in autoimmune hepatitis and chronic hepatitis C identifies similarities in patients with severe disease
title_full_unstemmed Autoantibody profiles in autoimmune hepatitis and chronic hepatitis C identifies similarities in patients with severe disease
title_short Autoantibody profiles in autoimmune hepatitis and chronic hepatitis C identifies similarities in patients with severe disease
title_sort autoantibody profiles in autoimmune hepatitis and chronic hepatitis c identifies similarities in patients with severe disease
topic Basic Study
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5330819/
https://www.ncbi.nlm.nih.gov/pubmed/28293081
http://dx.doi.org/10.3748/wjg.v23.i8.1345
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