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Splenectomy induces biochemical remission and regeneration in experimental murine autoimmune hepatitis

Autoimmune hepatitis (AIH) is a chronic immune-mediated inflammatory liver disease. It is known that AIH originates not from the spleen but from the liver itself. Nonetheless, most details of the etiology and pathophysiology are unknown. We induced experimental murine AIH (emAIH) in NOD/Ltj mice by...

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Autores principales: Dywicki, Janine, Buitrago-Molina, Laura Elisa, Noyan, Fatih, Schlue, Jerome, Iordanidis, Konstantinos, Manns, Michael P., Wedemeyer, Heiner, Jaeckel, Elmar, Hardtke-Wolenski, Matthias
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9737750/
https://www.ncbi.nlm.nih.gov/pubmed/36496477
http://dx.doi.org/10.1186/s40001-022-00933-3
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author Dywicki, Janine
Buitrago-Molina, Laura Elisa
Noyan, Fatih
Schlue, Jerome
Iordanidis, Konstantinos
Manns, Michael P.
Wedemeyer, Heiner
Jaeckel, Elmar
Hardtke-Wolenski, Matthias
author_facet Dywicki, Janine
Buitrago-Molina, Laura Elisa
Noyan, Fatih
Schlue, Jerome
Iordanidis, Konstantinos
Manns, Michael P.
Wedemeyer, Heiner
Jaeckel, Elmar
Hardtke-Wolenski, Matthias
author_sort Dywicki, Janine
collection PubMed
description Autoimmune hepatitis (AIH) is a chronic immune-mediated inflammatory liver disease. It is known that AIH originates not from the spleen but from the liver itself. Nonetheless, most details of the etiology and pathophysiology are unknown. We induced experimental murine AIH (emAIH) in NOD/Ltj mice by single administration of a replication-deficient adenovirus and performed splenectomy during late-stage disease. Biochemical disease remission occurred, which was characterized by improvement in transaminase levels. The causes of this remission included a shift in the transcriptomic signature of serum proteins toward regeneration. At the cellular level, there was a marked decrease in activated CD8(+) T cells and an increase in intrahepatic regulatory T cells (Tregs). Here, intrahepatic Treg numbers correlated with biochemical remission. Notably, an imbalance in the T-cell/B-cell ratio was observed, with a disproportionate increase in total B cells. In summary, intrahepatic increases in Tregs, biochemical remission, and regeneration could be induced by splenectomy in the late stage of emAIH.
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spelling pubmed-97377502022-12-11 Splenectomy induces biochemical remission and regeneration in experimental murine autoimmune hepatitis Dywicki, Janine Buitrago-Molina, Laura Elisa Noyan, Fatih Schlue, Jerome Iordanidis, Konstantinos Manns, Michael P. Wedemeyer, Heiner Jaeckel, Elmar Hardtke-Wolenski, Matthias Eur J Med Res Research Autoimmune hepatitis (AIH) is a chronic immune-mediated inflammatory liver disease. It is known that AIH originates not from the spleen but from the liver itself. Nonetheless, most details of the etiology and pathophysiology are unknown. We induced experimental murine AIH (emAIH) in NOD/Ltj mice by single administration of a replication-deficient adenovirus and performed splenectomy during late-stage disease. Biochemical disease remission occurred, which was characterized by improvement in transaminase levels. The causes of this remission included a shift in the transcriptomic signature of serum proteins toward regeneration. At the cellular level, there was a marked decrease in activated CD8(+) T cells and an increase in intrahepatic regulatory T cells (Tregs). Here, intrahepatic Treg numbers correlated with biochemical remission. Notably, an imbalance in the T-cell/B-cell ratio was observed, with a disproportionate increase in total B cells. In summary, intrahepatic increases in Tregs, biochemical remission, and regeneration could be induced by splenectomy in the late stage of emAIH. BioMed Central 2022-12-10 /pmc/articles/PMC9737750/ /pubmed/36496477 http://dx.doi.org/10.1186/s40001-022-00933-3 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Dywicki, Janine
Buitrago-Molina, Laura Elisa
Noyan, Fatih
Schlue, Jerome
Iordanidis, Konstantinos
Manns, Michael P.
Wedemeyer, Heiner
Jaeckel, Elmar
Hardtke-Wolenski, Matthias
Splenectomy induces biochemical remission and regeneration in experimental murine autoimmune hepatitis
title Splenectomy induces biochemical remission and regeneration in experimental murine autoimmune hepatitis
title_full Splenectomy induces biochemical remission and regeneration in experimental murine autoimmune hepatitis
title_fullStr Splenectomy induces biochemical remission and regeneration in experimental murine autoimmune hepatitis
title_full_unstemmed Splenectomy induces biochemical remission and regeneration in experimental murine autoimmune hepatitis
title_short Splenectomy induces biochemical remission and regeneration in experimental murine autoimmune hepatitis
title_sort splenectomy induces biochemical remission and regeneration in experimental murine autoimmune hepatitis
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9737750/
https://www.ncbi.nlm.nih.gov/pubmed/36496477
http://dx.doi.org/10.1186/s40001-022-00933-3
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