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The Impact of a CMV Infection on the Expression of Selected Immunological Parameters in Liver Tissue in Children with Biliary Atresia

The pathogenesis of biliary atresia (BA) is still not clear. The aim of this study was to evaluate the expression of selected immunological parameters in liver tissue in BA children based on CMV/EBV infection status. Eight of thirty-one children with newly diagnosed BA were included in this prospect...

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Autores principales: Janowska, Maria, Bierła, Joanna B., Kaleta, Magdalena, Wierzbicka-Rucińska, Aldona, Czubkowski, Piotr, Kanarek, Ewelina, Cukrowska, Bożena, Pawłowska, Joanna, Cielecka-Kuszyk, Joanna
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9781492/
https://www.ncbi.nlm.nih.gov/pubmed/36555887
http://dx.doi.org/10.3390/jcm11247269
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author Janowska, Maria
Bierła, Joanna B.
Kaleta, Magdalena
Wierzbicka-Rucińska, Aldona
Czubkowski, Piotr
Kanarek, Ewelina
Cukrowska, Bożena
Pawłowska, Joanna
Cielecka-Kuszyk, Joanna
author_facet Janowska, Maria
Bierła, Joanna B.
Kaleta, Magdalena
Wierzbicka-Rucińska, Aldona
Czubkowski, Piotr
Kanarek, Ewelina
Cukrowska, Bożena
Pawłowska, Joanna
Cielecka-Kuszyk, Joanna
author_sort Janowska, Maria
collection PubMed
description The pathogenesis of biliary atresia (BA) is still not clear. The aim of this study was to evaluate the expression of selected immunological parameters in liver tissue in BA children based on CMV/EBV infection status. Eight of thirty-one children with newly diagnosed BA were included in this prospective study and assigned to two groups (I with active infection, II without active or past infection). All studies were performed on surgical liver biopsies. To visualize CD8+ T cells and CD56 expression, immunohistochemical staining was performed. The viral genetic material in the studied groups was not found, but CMV infection significantly affected the number of CD8+ lymphocytes in both the portal area and the bile ducts. The average number of CD8+ cells per mm(2) of portal area in Groups I and II was 335 and 200 (p = 0.002). The average number of these cellsthat infiltrated the epithelium of the bile duct per mm(2) in Group I and II was 0.73 and 0.37 (p = 0.0003), respectively. Expression of CD56 in the bile ducts corresponded to the intensity of the inflammatory infiltrate of CD8+ cells. Our results suggest that active CMV infection induces an increased infiltration of CD8+ lymphocytes, which could play a role in BA immunopathogenesis. Increased CD56 expression can be a sign of a newly formed bile structure often without lumen, suggesting inhibition of the maturation process in BA.
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spelling pubmed-97814922022-12-24 The Impact of a CMV Infection on the Expression of Selected Immunological Parameters in Liver Tissue in Children with Biliary Atresia Janowska, Maria Bierła, Joanna B. Kaleta, Magdalena Wierzbicka-Rucińska, Aldona Czubkowski, Piotr Kanarek, Ewelina Cukrowska, Bożena Pawłowska, Joanna Cielecka-Kuszyk, Joanna J Clin Med Article The pathogenesis of biliary atresia (BA) is still not clear. The aim of this study was to evaluate the expression of selected immunological parameters in liver tissue in BA children based on CMV/EBV infection status. Eight of thirty-one children with newly diagnosed BA were included in this prospective study and assigned to two groups (I with active infection, II without active or past infection). All studies were performed on surgical liver biopsies. To visualize CD8+ T cells and CD56 expression, immunohistochemical staining was performed. The viral genetic material in the studied groups was not found, but CMV infection significantly affected the number of CD8+ lymphocytes in both the portal area and the bile ducts. The average number of CD8+ cells per mm(2) of portal area in Groups I and II was 335 and 200 (p = 0.002). The average number of these cellsthat infiltrated the epithelium of the bile duct per mm(2) in Group I and II was 0.73 and 0.37 (p = 0.0003), respectively. Expression of CD56 in the bile ducts corresponded to the intensity of the inflammatory infiltrate of CD8+ cells. Our results suggest that active CMV infection induces an increased infiltration of CD8+ lymphocytes, which could play a role in BA immunopathogenesis. Increased CD56 expression can be a sign of a newly formed bile structure often without lumen, suggesting inhibition of the maturation process in BA. MDPI 2022-12-07 /pmc/articles/PMC9781492/ /pubmed/36555887 http://dx.doi.org/10.3390/jcm11247269 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Janowska, Maria
Bierła, Joanna B.
Kaleta, Magdalena
Wierzbicka-Rucińska, Aldona
Czubkowski, Piotr
Kanarek, Ewelina
Cukrowska, Bożena
Pawłowska, Joanna
Cielecka-Kuszyk, Joanna
The Impact of a CMV Infection on the Expression of Selected Immunological Parameters in Liver Tissue in Children with Biliary Atresia
title The Impact of a CMV Infection on the Expression of Selected Immunological Parameters in Liver Tissue in Children with Biliary Atresia
title_full The Impact of a CMV Infection on the Expression of Selected Immunological Parameters in Liver Tissue in Children with Biliary Atresia
title_fullStr The Impact of a CMV Infection on the Expression of Selected Immunological Parameters in Liver Tissue in Children with Biliary Atresia
title_full_unstemmed The Impact of a CMV Infection on the Expression of Selected Immunological Parameters in Liver Tissue in Children with Biliary Atresia
title_short The Impact of a CMV Infection on the Expression of Selected Immunological Parameters in Liver Tissue in Children with Biliary Atresia
title_sort impact of a cmv infection on the expression of selected immunological parameters in liver tissue in children with biliary atresia
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9781492/
https://www.ncbi.nlm.nih.gov/pubmed/36555887
http://dx.doi.org/10.3390/jcm11247269
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