A protective effect of inflammatory bowel disease on the severity of sclerosing cholangitis
BackgroundPrimary sclerosing cholangitis (PSC) is a chronic liver disease marked by inflammation of the bile ducts and results in the development of strictures and fibrosis. A robust clinical correlation exists between PSC and inflammatory bowel disease (IBD). At present, published data are controve...
Ausführliche Beschreibung
Autor*in: |
Friederike Stumme [verfasserIn] Niklas Steffens [verfasserIn] Babett Steglich [verfasserIn] Franziska Mathies [verfasserIn] Mikolaj Nawrocki [verfasserIn] Morsal Sabihi [verfasserIn] Shiwa Soukou-Wargalla [verfasserIn] Emilia Göke [verfasserIn] Jan Kempski [verfasserIn] Thorben Fründt [verfasserIn] Sören Weidemann [verfasserIn] Christoph Schramm [verfasserIn] Nicola Gagliani [verfasserIn] Samuel Huber [verfasserIn] Tanja Bedke [verfasserIn] |
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E-Artikel |
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Sprache: |
Englisch |
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2024 |
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Übergeordnetes Werk: |
In: Frontiers in Immunology - Frontiers Media S.A., 2011, 15(2024) |
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Übergeordnetes Werk: |
volume:15 ; year:2024 |
Links: |
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DOI / URN: |
10.3389/fimmu.2024.1307297 |
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Katalog-ID: |
DOAJ099734036 |
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520 | |a BackgroundPrimary sclerosing cholangitis (PSC) is a chronic liver disease marked by inflammation of the bile ducts and results in the development of strictures and fibrosis. A robust clinical correlation exists between PSC and inflammatory bowel disease (IBD). At present, published data are controversial, and it is yet unclear whether IBD drives or attenuates PSC.MethodsMdr2-deficient mice or DDC-fed mice were used as experimental models for sclerosing cholangitis. Additionally, colitis was induced in mice with experimental sclerosing cholangitis, either through infection with Citrobacter rodentium or by feeding with DSS. Lastly, fibrosis levels were determined through FibroScan analysis in people with PSC and PSC-IBD.ResultsUsing two distinct experimental models of colitis and two models of sclerosing cholangitis, we found that colitis does not aggravate liver pathology, but rather reduces liver inflammation and liver fibrosis. Likewise, people with PSC-IBD have decreased liver fibrosis compared to those with PSC alone.ConclusionsWe found evidence that intestinal inflammation attenuates liver pathology. This study serves as a basis for further research on the pathogenesis of PSC and PSC-IBD, as well as the molecular mechanism responsible for the protective effect of IBD on PSC development. This study could lead to the discovery of novel therapeutic targets for PSC. | ||
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10.3389/fimmu.2024.1307297 doi (DE-627)DOAJ099734036 (DE-599)DOAJfe4be545b6ce4708b789790c53a8eb4c DE-627 ger DE-627 rakwb eng RC581-607 Friederike Stumme verfasserin aut A protective effect of inflammatory bowel disease on the severity of sclerosing cholangitis 2024 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier BackgroundPrimary sclerosing cholangitis (PSC) is a chronic liver disease marked by inflammation of the bile ducts and results in the development of strictures and fibrosis. A robust clinical correlation exists between PSC and inflammatory bowel disease (IBD). At present, published data are controversial, and it is yet unclear whether IBD drives or attenuates PSC.MethodsMdr2-deficient mice or DDC-fed mice were used as experimental models for sclerosing cholangitis. Additionally, colitis was induced in mice with experimental sclerosing cholangitis, either through infection with Citrobacter rodentium or by feeding with DSS. Lastly, fibrosis levels were determined through FibroScan analysis in people with PSC and PSC-IBD.ResultsUsing two distinct experimental models of colitis and two models of sclerosing cholangitis, we found that colitis does not aggravate liver pathology, but rather reduces liver inflammation and liver fibrosis. Likewise, people with PSC-IBD have decreased liver fibrosis compared to those with PSC alone.ConclusionsWe found evidence that intestinal inflammation attenuates liver pathology. This study serves as a basis for further research on the pathogenesis of PSC and PSC-IBD, as well as the molecular mechanism responsible for the protective effect of IBD on PSC development. This study could lead to the discovery of novel therapeutic targets for PSC. primary sclerosing cholangitis inflammatory bowel disease Mdr2 knock out microbiota colitis Immunologic diseases. Allergy Friederike Stumme verfasserin aut Niklas Steffens verfasserin aut Babett Steglich verfasserin aut Babett Steglich verfasserin aut Babett Steglich verfasserin aut Franziska Mathies verfasserin aut Mikolaj Nawrocki verfasserin aut Mikolaj Nawrocki verfasserin aut Morsal Sabihi verfasserin aut Morsal Sabihi verfasserin aut Shiwa Soukou-Wargalla verfasserin aut Emilia Göke verfasserin aut Emilia Göke verfasserin aut Jan Kempski verfasserin aut Jan Kempski verfasserin aut Thorben Fründt verfasserin aut Sören Weidemann verfasserin aut Christoph Schramm verfasserin aut Christoph Schramm verfasserin aut Christoph Schramm verfasserin aut Nicola Gagliani verfasserin aut Nicola Gagliani verfasserin aut Nicola Gagliani verfasserin aut Samuel Huber verfasserin aut Samuel Huber verfasserin aut Tanja Bedke verfasserin aut Tanja Bedke verfasserin aut In Frontiers in Immunology Frontiers Media S.A., 2011 15(2024) (DE-627)657998354 (DE-600)2606827-8 16643224 nnns volume:15 year:2024 https://doi.org/10.3389/fimmu.2024.1307297 kostenfrei https://doaj.org/article/fe4be545b6ce4708b789790c53a8eb4c kostenfrei https://www.frontiersin.org/articles/10.3389/fimmu.2024.1307297/full kostenfrei https://doaj.org/toc/1664-3224 Journal toc kostenfrei GBV_USEFLAG_A SYSFLAG_A GBV_DOAJ GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_73 GBV_ILN_74 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_206 GBV_ILN_213 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_2003 GBV_ILN_2014 GBV_ILN_4012 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4249 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 AR 15 2024 |
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10.3389/fimmu.2024.1307297 doi (DE-627)DOAJ099734036 (DE-599)DOAJfe4be545b6ce4708b789790c53a8eb4c DE-627 ger DE-627 rakwb eng RC581-607 Friederike Stumme verfasserin aut A protective effect of inflammatory bowel disease on the severity of sclerosing cholangitis 2024 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier BackgroundPrimary sclerosing cholangitis (PSC) is a chronic liver disease marked by inflammation of the bile ducts and results in the development of strictures and fibrosis. A robust clinical correlation exists between PSC and inflammatory bowel disease (IBD). At present, published data are controversial, and it is yet unclear whether IBD drives or attenuates PSC.MethodsMdr2-deficient mice or DDC-fed mice were used as experimental models for sclerosing cholangitis. Additionally, colitis was induced in mice with experimental sclerosing cholangitis, either through infection with Citrobacter rodentium or by feeding with DSS. Lastly, fibrosis levels were determined through FibroScan analysis in people with PSC and PSC-IBD.ResultsUsing two distinct experimental models of colitis and two models of sclerosing cholangitis, we found that colitis does not aggravate liver pathology, but rather reduces liver inflammation and liver fibrosis. Likewise, people with PSC-IBD have decreased liver fibrosis compared to those with PSC alone.ConclusionsWe found evidence that intestinal inflammation attenuates liver pathology. This study serves as a basis for further research on the pathogenesis of PSC and PSC-IBD, as well as the molecular mechanism responsible for the protective effect of IBD on PSC development. This study could lead to the discovery of novel therapeutic targets for PSC. primary sclerosing cholangitis inflammatory bowel disease Mdr2 knock out microbiota colitis Immunologic diseases. Allergy Friederike Stumme verfasserin aut Niklas Steffens verfasserin aut Babett Steglich verfasserin aut Babett Steglich verfasserin aut Babett Steglich verfasserin aut Franziska Mathies verfasserin aut Mikolaj Nawrocki verfasserin aut Mikolaj Nawrocki verfasserin aut Morsal Sabihi verfasserin aut Morsal Sabihi verfasserin aut Shiwa Soukou-Wargalla verfasserin aut Emilia Göke verfasserin aut Emilia Göke verfasserin aut Jan Kempski verfasserin aut Jan Kempski verfasserin aut Thorben Fründt verfasserin aut Sören Weidemann verfasserin aut Christoph Schramm verfasserin aut Christoph Schramm verfasserin aut Christoph Schramm verfasserin aut Nicola Gagliani verfasserin aut Nicola Gagliani verfasserin aut Nicola Gagliani verfasserin aut Samuel Huber verfasserin aut Samuel Huber verfasserin aut Tanja Bedke verfasserin aut Tanja Bedke verfasserin aut In Frontiers in Immunology Frontiers Media S.A., 2011 15(2024) (DE-627)657998354 (DE-600)2606827-8 16643224 nnns volume:15 year:2024 https://doi.org/10.3389/fimmu.2024.1307297 kostenfrei https://doaj.org/article/fe4be545b6ce4708b789790c53a8eb4c kostenfrei https://www.frontiersin.org/articles/10.3389/fimmu.2024.1307297/full kostenfrei https://doaj.org/toc/1664-3224 Journal toc kostenfrei GBV_USEFLAG_A SYSFLAG_A GBV_DOAJ GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_73 GBV_ILN_74 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_206 GBV_ILN_213 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_2003 GBV_ILN_2014 GBV_ILN_4012 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4249 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 AR 15 2024 |
allfields_unstemmed |
10.3389/fimmu.2024.1307297 doi (DE-627)DOAJ099734036 (DE-599)DOAJfe4be545b6ce4708b789790c53a8eb4c DE-627 ger DE-627 rakwb eng RC581-607 Friederike Stumme verfasserin aut A protective effect of inflammatory bowel disease on the severity of sclerosing cholangitis 2024 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier BackgroundPrimary sclerosing cholangitis (PSC) is a chronic liver disease marked by inflammation of the bile ducts and results in the development of strictures and fibrosis. A robust clinical correlation exists between PSC and inflammatory bowel disease (IBD). At present, published data are controversial, and it is yet unclear whether IBD drives or attenuates PSC.MethodsMdr2-deficient mice or DDC-fed mice were used as experimental models for sclerosing cholangitis. Additionally, colitis was induced in mice with experimental sclerosing cholangitis, either through infection with Citrobacter rodentium or by feeding with DSS. Lastly, fibrosis levels were determined through FibroScan analysis in people with PSC and PSC-IBD.ResultsUsing two distinct experimental models of colitis and two models of sclerosing cholangitis, we found that colitis does not aggravate liver pathology, but rather reduces liver inflammation and liver fibrosis. Likewise, people with PSC-IBD have decreased liver fibrosis compared to those with PSC alone.ConclusionsWe found evidence that intestinal inflammation attenuates liver pathology. This study serves as a basis for further research on the pathogenesis of PSC and PSC-IBD, as well as the molecular mechanism responsible for the protective effect of IBD on PSC development. This study could lead to the discovery of novel therapeutic targets for PSC. primary sclerosing cholangitis inflammatory bowel disease Mdr2 knock out microbiota colitis Immunologic diseases. Allergy Friederike Stumme verfasserin aut Niklas Steffens verfasserin aut Babett Steglich verfasserin aut Babett Steglich verfasserin aut Babett Steglich verfasserin aut Franziska Mathies verfasserin aut Mikolaj Nawrocki verfasserin aut Mikolaj Nawrocki verfasserin aut Morsal Sabihi verfasserin aut Morsal Sabihi verfasserin aut Shiwa Soukou-Wargalla verfasserin aut Emilia Göke verfasserin aut Emilia Göke verfasserin aut Jan Kempski verfasserin aut Jan Kempski verfasserin aut Thorben Fründt verfasserin aut Sören Weidemann verfasserin aut Christoph Schramm verfasserin aut Christoph Schramm verfasserin aut Christoph Schramm verfasserin aut Nicola Gagliani verfasserin aut Nicola Gagliani verfasserin aut Nicola Gagliani verfasserin aut Samuel Huber verfasserin aut Samuel Huber verfasserin aut Tanja Bedke verfasserin aut Tanja Bedke verfasserin aut In Frontiers in Immunology Frontiers Media S.A., 2011 15(2024) (DE-627)657998354 (DE-600)2606827-8 16643224 nnns volume:15 year:2024 https://doi.org/10.3389/fimmu.2024.1307297 kostenfrei https://doaj.org/article/fe4be545b6ce4708b789790c53a8eb4c kostenfrei https://www.frontiersin.org/articles/10.3389/fimmu.2024.1307297/full kostenfrei https://doaj.org/toc/1664-3224 Journal toc kostenfrei GBV_USEFLAG_A SYSFLAG_A GBV_DOAJ GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_73 GBV_ILN_74 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_206 GBV_ILN_213 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_2003 GBV_ILN_2014 GBV_ILN_4012 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4249 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 AR 15 2024 |
allfieldsGer |
10.3389/fimmu.2024.1307297 doi (DE-627)DOAJ099734036 (DE-599)DOAJfe4be545b6ce4708b789790c53a8eb4c DE-627 ger DE-627 rakwb eng RC581-607 Friederike Stumme verfasserin aut A protective effect of inflammatory bowel disease on the severity of sclerosing cholangitis 2024 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier BackgroundPrimary sclerosing cholangitis (PSC) is a chronic liver disease marked by inflammation of the bile ducts and results in the development of strictures and fibrosis. A robust clinical correlation exists between PSC and inflammatory bowel disease (IBD). At present, published data are controversial, and it is yet unclear whether IBD drives or attenuates PSC.MethodsMdr2-deficient mice or DDC-fed mice were used as experimental models for sclerosing cholangitis. Additionally, colitis was induced in mice with experimental sclerosing cholangitis, either through infection with Citrobacter rodentium or by feeding with DSS. Lastly, fibrosis levels were determined through FibroScan analysis in people with PSC and PSC-IBD.ResultsUsing two distinct experimental models of colitis and two models of sclerosing cholangitis, we found that colitis does not aggravate liver pathology, but rather reduces liver inflammation and liver fibrosis. Likewise, people with PSC-IBD have decreased liver fibrosis compared to those with PSC alone.ConclusionsWe found evidence that intestinal inflammation attenuates liver pathology. This study serves as a basis for further research on the pathogenesis of PSC and PSC-IBD, as well as the molecular mechanism responsible for the protective effect of IBD on PSC development. This study could lead to the discovery of novel therapeutic targets for PSC. primary sclerosing cholangitis inflammatory bowel disease Mdr2 knock out microbiota colitis Immunologic diseases. Allergy Friederike Stumme verfasserin aut Niklas Steffens verfasserin aut Babett Steglich verfasserin aut Babett Steglich verfasserin aut Babett Steglich verfasserin aut Franziska Mathies verfasserin aut Mikolaj Nawrocki verfasserin aut Mikolaj Nawrocki verfasserin aut Morsal Sabihi verfasserin aut Morsal Sabihi verfasserin aut Shiwa Soukou-Wargalla verfasserin aut Emilia Göke verfasserin aut Emilia Göke verfasserin aut Jan Kempski verfasserin aut Jan Kempski verfasserin aut Thorben Fründt verfasserin aut Sören Weidemann verfasserin aut Christoph Schramm verfasserin aut Christoph Schramm verfasserin aut Christoph Schramm verfasserin aut Nicola Gagliani verfasserin aut Nicola Gagliani verfasserin aut Nicola Gagliani verfasserin aut Samuel Huber verfasserin aut Samuel Huber verfasserin aut Tanja Bedke verfasserin aut Tanja Bedke verfasserin aut In Frontiers in Immunology Frontiers Media S.A., 2011 15(2024) (DE-627)657998354 (DE-600)2606827-8 16643224 nnns volume:15 year:2024 https://doi.org/10.3389/fimmu.2024.1307297 kostenfrei https://doaj.org/article/fe4be545b6ce4708b789790c53a8eb4c kostenfrei https://www.frontiersin.org/articles/10.3389/fimmu.2024.1307297/full kostenfrei https://doaj.org/toc/1664-3224 Journal toc kostenfrei GBV_USEFLAG_A SYSFLAG_A GBV_DOAJ GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_73 GBV_ILN_74 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_206 GBV_ILN_213 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_2003 GBV_ILN_2014 GBV_ILN_4012 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4249 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 AR 15 2024 |
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10.3389/fimmu.2024.1307297 doi (DE-627)DOAJ099734036 (DE-599)DOAJfe4be545b6ce4708b789790c53a8eb4c DE-627 ger DE-627 rakwb eng RC581-607 Friederike Stumme verfasserin aut A protective effect of inflammatory bowel disease on the severity of sclerosing cholangitis 2024 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier BackgroundPrimary sclerosing cholangitis (PSC) is a chronic liver disease marked by inflammation of the bile ducts and results in the development of strictures and fibrosis. A robust clinical correlation exists between PSC and inflammatory bowel disease (IBD). At present, published data are controversial, and it is yet unclear whether IBD drives or attenuates PSC.MethodsMdr2-deficient mice or DDC-fed mice were used as experimental models for sclerosing cholangitis. Additionally, colitis was induced in mice with experimental sclerosing cholangitis, either through infection with Citrobacter rodentium or by feeding with DSS. Lastly, fibrosis levels were determined through FibroScan analysis in people with PSC and PSC-IBD.ResultsUsing two distinct experimental models of colitis and two models of sclerosing cholangitis, we found that colitis does not aggravate liver pathology, but rather reduces liver inflammation and liver fibrosis. Likewise, people with PSC-IBD have decreased liver fibrosis compared to those with PSC alone.ConclusionsWe found evidence that intestinal inflammation attenuates liver pathology. This study serves as a basis for further research on the pathogenesis of PSC and PSC-IBD, as well as the molecular mechanism responsible for the protective effect of IBD on PSC development. This study could lead to the discovery of novel therapeutic targets for PSC. primary sclerosing cholangitis inflammatory bowel disease Mdr2 knock out microbiota colitis Immunologic diseases. Allergy Friederike Stumme verfasserin aut Niklas Steffens verfasserin aut Babett Steglich verfasserin aut Babett Steglich verfasserin aut Babett Steglich verfasserin aut Franziska Mathies verfasserin aut Mikolaj Nawrocki verfasserin aut Mikolaj Nawrocki verfasserin aut Morsal Sabihi verfasserin aut Morsal Sabihi verfasserin aut Shiwa Soukou-Wargalla verfasserin aut Emilia Göke verfasserin aut Emilia Göke verfasserin aut Jan Kempski verfasserin aut Jan Kempski verfasserin aut Thorben Fründt verfasserin aut Sören Weidemann verfasserin aut Christoph Schramm verfasserin aut Christoph Schramm verfasserin aut Christoph Schramm verfasserin aut Nicola Gagliani verfasserin aut Nicola Gagliani verfasserin aut Nicola Gagliani verfasserin aut Samuel Huber verfasserin aut Samuel Huber verfasserin aut Tanja Bedke verfasserin aut Tanja Bedke verfasserin aut In Frontiers in Immunology Frontiers Media S.A., 2011 15(2024) (DE-627)657998354 (DE-600)2606827-8 16643224 nnns volume:15 year:2024 https://doi.org/10.3389/fimmu.2024.1307297 kostenfrei https://doaj.org/article/fe4be545b6ce4708b789790c53a8eb4c kostenfrei https://www.frontiersin.org/articles/10.3389/fimmu.2024.1307297/full kostenfrei https://doaj.org/toc/1664-3224 Journal toc kostenfrei GBV_USEFLAG_A SYSFLAG_A GBV_DOAJ GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_73 GBV_ILN_74 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_206 GBV_ILN_213 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_2003 GBV_ILN_2014 GBV_ILN_4012 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4249 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 AR 15 2024 |
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Friederike Stumme @@aut@@ Niklas Steffens @@aut@@ Babett Steglich @@aut@@ Franziska Mathies @@aut@@ Mikolaj Nawrocki @@aut@@ Morsal Sabihi @@aut@@ Shiwa Soukou-Wargalla @@aut@@ Emilia Göke @@aut@@ Jan Kempski @@aut@@ Thorben Fründt @@aut@@ Sören Weidemann @@aut@@ Christoph Schramm @@aut@@ Nicola Gagliani @@aut@@ Samuel Huber @@aut@@ Tanja Bedke @@aut@@ |
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RC581-607 A protective effect of inflammatory bowel disease on the severity of sclerosing cholangitis primary sclerosing cholangitis inflammatory bowel disease Mdr2 knock out microbiota colitis |
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A protective effect of inflammatory bowel disease on the severity of sclerosing cholangitis |
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A protective effect of inflammatory bowel disease on the severity of sclerosing cholangitis |
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Friederike Stumme |
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Friederike Stumme Niklas Steffens Babett Steglich Franziska Mathies Mikolaj Nawrocki Morsal Sabihi Shiwa Soukou-Wargalla Emilia Göke Jan Kempski Thorben Fründt Sören Weidemann Christoph Schramm Nicola Gagliani Samuel Huber Tanja Bedke |
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protective effect of inflammatory bowel disease on the severity of sclerosing cholangitis |
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A protective effect of inflammatory bowel disease on the severity of sclerosing cholangitis |
abstract |
BackgroundPrimary sclerosing cholangitis (PSC) is a chronic liver disease marked by inflammation of the bile ducts and results in the development of strictures and fibrosis. A robust clinical correlation exists between PSC and inflammatory bowel disease (IBD). At present, published data are controversial, and it is yet unclear whether IBD drives or attenuates PSC.MethodsMdr2-deficient mice or DDC-fed mice were used as experimental models for sclerosing cholangitis. Additionally, colitis was induced in mice with experimental sclerosing cholangitis, either through infection with Citrobacter rodentium or by feeding with DSS. Lastly, fibrosis levels were determined through FibroScan analysis in people with PSC and PSC-IBD.ResultsUsing two distinct experimental models of colitis and two models of sclerosing cholangitis, we found that colitis does not aggravate liver pathology, but rather reduces liver inflammation and liver fibrosis. Likewise, people with PSC-IBD have decreased liver fibrosis compared to those with PSC alone.ConclusionsWe found evidence that intestinal inflammation attenuates liver pathology. This study serves as a basis for further research on the pathogenesis of PSC and PSC-IBD, as well as the molecular mechanism responsible for the protective effect of IBD on PSC development. This study could lead to the discovery of novel therapeutic targets for PSC. |
abstractGer |
BackgroundPrimary sclerosing cholangitis (PSC) is a chronic liver disease marked by inflammation of the bile ducts and results in the development of strictures and fibrosis. A robust clinical correlation exists between PSC and inflammatory bowel disease (IBD). At present, published data are controversial, and it is yet unclear whether IBD drives or attenuates PSC.MethodsMdr2-deficient mice or DDC-fed mice were used as experimental models for sclerosing cholangitis. Additionally, colitis was induced in mice with experimental sclerosing cholangitis, either through infection with Citrobacter rodentium or by feeding with DSS. Lastly, fibrosis levels were determined through FibroScan analysis in people with PSC and PSC-IBD.ResultsUsing two distinct experimental models of colitis and two models of sclerosing cholangitis, we found that colitis does not aggravate liver pathology, but rather reduces liver inflammation and liver fibrosis. Likewise, people with PSC-IBD have decreased liver fibrosis compared to those with PSC alone.ConclusionsWe found evidence that intestinal inflammation attenuates liver pathology. This study serves as a basis for further research on the pathogenesis of PSC and PSC-IBD, as well as the molecular mechanism responsible for the protective effect of IBD on PSC development. This study could lead to the discovery of novel therapeutic targets for PSC. |
abstract_unstemmed |
BackgroundPrimary sclerosing cholangitis (PSC) is a chronic liver disease marked by inflammation of the bile ducts and results in the development of strictures and fibrosis. A robust clinical correlation exists between PSC and inflammatory bowel disease (IBD). At present, published data are controversial, and it is yet unclear whether IBD drives or attenuates PSC.MethodsMdr2-deficient mice or DDC-fed mice were used as experimental models for sclerosing cholangitis. Additionally, colitis was induced in mice with experimental sclerosing cholangitis, either through infection with Citrobacter rodentium or by feeding with DSS. Lastly, fibrosis levels were determined through FibroScan analysis in people with PSC and PSC-IBD.ResultsUsing two distinct experimental models of colitis and two models of sclerosing cholangitis, we found that colitis does not aggravate liver pathology, but rather reduces liver inflammation and liver fibrosis. Likewise, people with PSC-IBD have decreased liver fibrosis compared to those with PSC alone.ConclusionsWe found evidence that intestinal inflammation attenuates liver pathology. This study serves as a basis for further research on the pathogenesis of PSC and PSC-IBD, as well as the molecular mechanism responsible for the protective effect of IBD on PSC development. This study could lead to the discovery of novel therapeutic targets for PSC. |
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title_short |
A protective effect of inflammatory bowel disease on the severity of sclerosing cholangitis |
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Friederike Stumme Niklas Steffens Babett Steglich Franziska Mathies Mikolaj Nawrocki Morsal Sabihi Shiwa Soukou-Wargalla Emilia Göke Jan Kempski Thorben Fründt Sören Weidemann Christoph Schramm Nicola Gagliani Samuel Huber Tanja Bedke |
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