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Liver transplantation reverses hypergammaglobulinemia in patients with chronic hepatic failure

INTRODUCTION: Sparse data are available about the effect of therapy methods on antibody levels in patients with liver failure. The aim of this study was to determine serum immunoglobulin concentrations in patients with chronic hepatic failure (CHF), acute- (ALF), or acute-on-chronic liver failure (A...

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Autores principales: Lebherz-Eichinger, Diana, Schwarzer, Remy, Motal, Michael C., Klaus, Daniel A., Mangold, Andreas, Ankersmit, Hendrik J., Berlakovich, Gabriela A., Krenn, Claus G., Roth, Georg A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Croatian Society of Medical Biochemistry and Laboratory Medicine 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4470094/
https://www.ncbi.nlm.nih.gov/pubmed/26110038
http://dx.doi.org/10.11613/BM.2015.026
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author Lebherz-Eichinger, Diana
Schwarzer, Remy
Motal, Michael C.
Klaus, Daniel A.
Mangold, Andreas
Ankersmit, Hendrik J.
Berlakovich, Gabriela A.
Krenn, Claus G.
Roth, Georg A.
author_facet Lebherz-Eichinger, Diana
Schwarzer, Remy
Motal, Michael C.
Klaus, Daniel A.
Mangold, Andreas
Ankersmit, Hendrik J.
Berlakovich, Gabriela A.
Krenn, Claus G.
Roth, Georg A.
author_sort Lebherz-Eichinger, Diana
collection PubMed
description INTRODUCTION: Sparse data are available about the effect of therapy methods on antibody levels in patients with liver failure. The aim of this study was to determine serum immunoglobulin concentrations in patients with chronic hepatic failure (CHF), acute- (ALF), or acute-on-chronic liver failure (ACLF) and to evaluate the impact of MARS treatment or liver transplantation (LT) on antibody levels. MATERIALS AND METHODS: We followed ten patients with ALF, twelve with ACLF and 18 with CHF. Eight patients with ALF and seven with ACLF underwent MARS therapy, whereas the rest received LT. 13 healthy volunteers served as controls. Serum antibody concentrations were measured using ELISA-technique. RESULTS: Median serum levels of IgA, IgG and IgM were significantly increased in patients with CHF compared to ALF or controls (P < 0.02, P < 0.01, and P < 0.01). IgM and IgG concentrations were also significantly elevated in patients with CHF compared to ACLF (IgM, 3.7 vs. 1 g/L, P < 0.001; IgG, 8.7 vs. 3.1 g/L, P = 0.004). Immediately after LT a significant decrease of IgA (6.9 vs. 3.1 g/L, P = 0.004), IgG (8.7 vs. 5.1 g/L, P = 0.02) and IgM (3.7 vs. 1.8 g/L, P = 0.001) was detected in patients with CHF and antibody levels further decreased the days after LT reaching levels comparable to healthy individuals. MARS treatment had no apparent effect on the immunoglobulin profile in patients with ALF or ACLF. CONCLUSION: We provide evidence that LT reverses hypergammaglobulinemia in patients suffering from CHF within one day, which could be explained to a reconstituted hepatic antibody clearance, whereas MARS treatment has no immediate effect on immunoglobulin levels.
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spelling pubmed-44700942015-06-24 Liver transplantation reverses hypergammaglobulinemia in patients with chronic hepatic failure Lebherz-Eichinger, Diana Schwarzer, Remy Motal, Michael C. Klaus, Daniel A. Mangold, Andreas Ankersmit, Hendrik J. Berlakovich, Gabriela A. Krenn, Claus G. Roth, Georg A. Biochem Med (Zagreb) Research Article INTRODUCTION: Sparse data are available about the effect of therapy methods on antibody levels in patients with liver failure. The aim of this study was to determine serum immunoglobulin concentrations in patients with chronic hepatic failure (CHF), acute- (ALF), or acute-on-chronic liver failure (ACLF) and to evaluate the impact of MARS treatment or liver transplantation (LT) on antibody levels. MATERIALS AND METHODS: We followed ten patients with ALF, twelve with ACLF and 18 with CHF. Eight patients with ALF and seven with ACLF underwent MARS therapy, whereas the rest received LT. 13 healthy volunteers served as controls. Serum antibody concentrations were measured using ELISA-technique. RESULTS: Median serum levels of IgA, IgG and IgM were significantly increased in patients with CHF compared to ALF or controls (P < 0.02, P < 0.01, and P < 0.01). IgM and IgG concentrations were also significantly elevated in patients with CHF compared to ACLF (IgM, 3.7 vs. 1 g/L, P < 0.001; IgG, 8.7 vs. 3.1 g/L, P = 0.004). Immediately after LT a significant decrease of IgA (6.9 vs. 3.1 g/L, P = 0.004), IgG (8.7 vs. 5.1 g/L, P = 0.02) and IgM (3.7 vs. 1.8 g/L, P = 0.001) was detected in patients with CHF and antibody levels further decreased the days after LT reaching levels comparable to healthy individuals. MARS treatment had no apparent effect on the immunoglobulin profile in patients with ALF or ACLF. CONCLUSION: We provide evidence that LT reverses hypergammaglobulinemia in patients suffering from CHF within one day, which could be explained to a reconstituted hepatic antibody clearance, whereas MARS treatment has no immediate effect on immunoglobulin levels. Croatian Society of Medical Biochemistry and Laboratory Medicine 2015-06-05 /pmc/articles/PMC4470094/ /pubmed/26110038 http://dx.doi.org/10.11613/BM.2015.026 Text en
spellingShingle Research Article
Lebherz-Eichinger, Diana
Schwarzer, Remy
Motal, Michael C.
Klaus, Daniel A.
Mangold, Andreas
Ankersmit, Hendrik J.
Berlakovich, Gabriela A.
Krenn, Claus G.
Roth, Georg A.
Liver transplantation reverses hypergammaglobulinemia in patients with chronic hepatic failure
title Liver transplantation reverses hypergammaglobulinemia in patients with chronic hepatic failure
title_full Liver transplantation reverses hypergammaglobulinemia in patients with chronic hepatic failure
title_fullStr Liver transplantation reverses hypergammaglobulinemia in patients with chronic hepatic failure
title_full_unstemmed Liver transplantation reverses hypergammaglobulinemia in patients with chronic hepatic failure
title_short Liver transplantation reverses hypergammaglobulinemia in patients with chronic hepatic failure
title_sort liver transplantation reverses hypergammaglobulinemia in patients with chronic hepatic failure
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4470094/
https://www.ncbi.nlm.nih.gov/pubmed/26110038
http://dx.doi.org/10.11613/BM.2015.026
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