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P Selectins and immunological profiles in HCV and Schistosoma mansoni induced chronic liver disease

BACKGROUND: Hepatitis C virus (HCV) and Schistosoma mansoni are major causes of chronic liver disease (CLD) in which immune alteration is common. Recent studies suggested that certain platelets and lymphocytes activation markers may have an impact on progression of CLD. This study aimed to evaluate...

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Autores principales: Kamel, Mahmoud M, A Fouad, Shawky, Basyoni, Maha MA
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4119237/
https://www.ncbi.nlm.nih.gov/pubmed/25066324
http://dx.doi.org/10.1186/1471-230X-14-132
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author Kamel, Mahmoud M
A Fouad, Shawky
Basyoni, Maha MA
author_facet Kamel, Mahmoud M
A Fouad, Shawky
Basyoni, Maha MA
author_sort Kamel, Mahmoud M
collection PubMed
description BACKGROUND: Hepatitis C virus (HCV) and Schistosoma mansoni are major causes of chronic liver disease (CLD) in which immune alteration is common. Recent studies suggested that certain platelets and lymphocytes activation markers may have an impact on progression of CLD. This study aimed to evaluate the potential of platelets and lymphocytes activation molecules expression on the pathogenesis of CLD in distinct or concomitant chronic HCV and schistosomiasis mansoni infections. METHODS: The study populations were divided into group-I: patients with chronic schistosomiasis mansoni, group-II: HCV patients without cirrhosis, group-III: patients with combined liver diseases without cirrhosis, group-IV: patients with chronic HCV and liver cirrhosis and group-V: Age and sex matched healthy individuals as normal controls. All groups were subjected to full clinical evaluation, ELISA anti-HCV antibodies screening, parasitological examination for diagnosing S. mansoni and flow cytometry for lymphocyte (CD3, CD4, CD8, CD19, CD22, & CD56) and platelets activation (CD41, CD42 & CD62P (P- selectins)) markers. RESULTS: The platelet count was significantly decreased in HCV and/or S. mansoni patients. The total T-lymphocytes and T-helper cells were significantly reduced, while T-cytotoxics were increased. The patients possessed a significantly higher platelets activation marker; CD62P (P-selectins) and higher mean fluorescent intensity (MFI) positivity. There were considerable correlations between platelets count and both of CD62P and MFI. CONCLUSION: Our Findings suggest an increased expression of certain platelets and lymphocytes activation markers in chronic HCV and S. mansoni induced CLD that may have a role in disease progression.
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spelling pubmed-41192372014-08-03 P Selectins and immunological profiles in HCV and Schistosoma mansoni induced chronic liver disease Kamel, Mahmoud M A Fouad, Shawky Basyoni, Maha MA BMC Gastroenterol Research Article BACKGROUND: Hepatitis C virus (HCV) and Schistosoma mansoni are major causes of chronic liver disease (CLD) in which immune alteration is common. Recent studies suggested that certain platelets and lymphocytes activation markers may have an impact on progression of CLD. This study aimed to evaluate the potential of platelets and lymphocytes activation molecules expression on the pathogenesis of CLD in distinct or concomitant chronic HCV and schistosomiasis mansoni infections. METHODS: The study populations were divided into group-I: patients with chronic schistosomiasis mansoni, group-II: HCV patients without cirrhosis, group-III: patients with combined liver diseases without cirrhosis, group-IV: patients with chronic HCV and liver cirrhosis and group-V: Age and sex matched healthy individuals as normal controls. All groups were subjected to full clinical evaluation, ELISA anti-HCV antibodies screening, parasitological examination for diagnosing S. mansoni and flow cytometry for lymphocyte (CD3, CD4, CD8, CD19, CD22, & CD56) and platelets activation (CD41, CD42 & CD62P (P- selectins)) markers. RESULTS: The platelet count was significantly decreased in HCV and/or S. mansoni patients. The total T-lymphocytes and T-helper cells were significantly reduced, while T-cytotoxics were increased. The patients possessed a significantly higher platelets activation marker; CD62P (P-selectins) and higher mean fluorescent intensity (MFI) positivity. There were considerable correlations between platelets count and both of CD62P and MFI. CONCLUSION: Our Findings suggest an increased expression of certain platelets and lymphocytes activation markers in chronic HCV and S. mansoni induced CLD that may have a role in disease progression. BioMed Central 2014-07-28 /pmc/articles/PMC4119237/ /pubmed/25066324 http://dx.doi.org/10.1186/1471-230X-14-132 Text en Copyright © 2014 Kamel et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/4.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Kamel, Mahmoud M
A Fouad, Shawky
Basyoni, Maha MA
P Selectins and immunological profiles in HCV and Schistosoma mansoni induced chronic liver disease
title P Selectins and immunological profiles in HCV and Schistosoma mansoni induced chronic liver disease
title_full P Selectins and immunological profiles in HCV and Schistosoma mansoni induced chronic liver disease
title_fullStr P Selectins and immunological profiles in HCV and Schistosoma mansoni induced chronic liver disease
title_full_unstemmed P Selectins and immunological profiles in HCV and Schistosoma mansoni induced chronic liver disease
title_short P Selectins and immunological profiles in HCV and Schistosoma mansoni induced chronic liver disease
title_sort p selectins and immunological profiles in hcv and schistosoma mansoni induced chronic liver disease
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4119237/
https://www.ncbi.nlm.nih.gov/pubmed/25066324
http://dx.doi.org/10.1186/1471-230X-14-132
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