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The role of hepatic progenitor cells in predicting response to therapy in Egyptian patients with chronic hepatitis C, genotype 4

BACKGROUND: Interferon therapy is used as a line of treatment of chronic hepatitis C virus (HCV) in several areas of the world including Egypt. OBJECTIVE: Our aim was to investigate the value of hepatic progenitor cells (HPCs) in predicting response of patients with chronic HCV, genotype 4 to pegyla...

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Autores principales: Helal, Thanaa El A, Radwan, Nehal A, Mahmoud, Heba A, Zaki, Ahmed ME, Ahmed, Naglaa S, Wahib, Ali AA, Aref, Ahmed M
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Makerere Medical School 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6531979/
https://www.ncbi.nlm.nih.gov/pubmed/31148968
http://dx.doi.org/10.4314/ahs.v19i1.14
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author Helal, Thanaa El A
Radwan, Nehal A
Mahmoud, Heba A
Zaki, Ahmed ME
Ahmed, Naglaa S
Wahib, Ali AA
Aref, Ahmed M
author_facet Helal, Thanaa El A
Radwan, Nehal A
Mahmoud, Heba A
Zaki, Ahmed ME
Ahmed, Naglaa S
Wahib, Ali AA
Aref, Ahmed M
author_sort Helal, Thanaa El A
collection PubMed
description BACKGROUND: Interferon therapy is used as a line of treatment of chronic hepatitis C virus (HCV) in several areas of the world including Egypt. OBJECTIVE: Our aim was to investigate the value of hepatic progenitor cells (HPCs) in predicting response of patients with chronic HCV, genotype 4 to pegylated interferon (PEGIFN) plus ribavirin (RBV) therapy. METHODS: Pre-treatment liver biopsies obtained from 110 patients with chronic HCV, genotype 4 were examined immunohistochemically for HPCs using cytokeratin19. The mean number of HPCs as ductular reaction (DR) and as isolated progenitor cells (IPCs) was counted in each case. The patients were classified into: those with sustained virological response (SVR) and those who did not achieve SVR. The results were compared between the two groups. Also, the relationships between HPCs and other clinico-pathologic variables were estimated using multivariate analysis. RESULTS: The mean number of HPCs was the only independent predictor of therapeutic response, being significantly higher in non-responders (P = 0 for DR and P = 0.03 for IPCs). On the other hand, fibrosis stage and steatosis were the only independent factors which showed a significant direct association with the mean number of HPCs in the form of DR and IPCs (P = 0 for each). CONCLUSION: The number of HPCs provides prognostic information in chronic HCV since it is significantly associated with stage of fibrosis. More importantly, it can be used as a marker to predict response of patients with chronic HCV to PEGIFN plus RBV therapy.
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spelling pubmed-65319792019-05-30 The role of hepatic progenitor cells in predicting response to therapy in Egyptian patients with chronic hepatitis C, genotype 4 Helal, Thanaa El A Radwan, Nehal A Mahmoud, Heba A Zaki, Ahmed ME Ahmed, Naglaa S Wahib, Ali AA Aref, Ahmed M Afr Health Sci Articles BACKGROUND: Interferon therapy is used as a line of treatment of chronic hepatitis C virus (HCV) in several areas of the world including Egypt. OBJECTIVE: Our aim was to investigate the value of hepatic progenitor cells (HPCs) in predicting response of patients with chronic HCV, genotype 4 to pegylated interferon (PEGIFN) plus ribavirin (RBV) therapy. METHODS: Pre-treatment liver biopsies obtained from 110 patients with chronic HCV, genotype 4 were examined immunohistochemically for HPCs using cytokeratin19. The mean number of HPCs as ductular reaction (DR) and as isolated progenitor cells (IPCs) was counted in each case. The patients were classified into: those with sustained virological response (SVR) and those who did not achieve SVR. The results were compared between the two groups. Also, the relationships between HPCs and other clinico-pathologic variables were estimated using multivariate analysis. RESULTS: The mean number of HPCs was the only independent predictor of therapeutic response, being significantly higher in non-responders (P = 0 for DR and P = 0.03 for IPCs). On the other hand, fibrosis stage and steatosis were the only independent factors which showed a significant direct association with the mean number of HPCs in the form of DR and IPCs (P = 0 for each). CONCLUSION: The number of HPCs provides prognostic information in chronic HCV since it is significantly associated with stage of fibrosis. More importantly, it can be used as a marker to predict response of patients with chronic HCV to PEGIFN plus RBV therapy. Makerere Medical School 2019-03 /pmc/articles/PMC6531979/ /pubmed/31148968 http://dx.doi.org/10.4314/ahs.v19i1.14 Text en © 2019 Helal et al. Licensee African Health Sciences. This is an Open Access article distributed under the terms of the Creative commons Attribution License (https://creativecommons.org/licenses/BY/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Articles
Helal, Thanaa El A
Radwan, Nehal A
Mahmoud, Heba A
Zaki, Ahmed ME
Ahmed, Naglaa S
Wahib, Ali AA
Aref, Ahmed M
The role of hepatic progenitor cells in predicting response to therapy in Egyptian patients with chronic hepatitis C, genotype 4
title The role of hepatic progenitor cells in predicting response to therapy in Egyptian patients with chronic hepatitis C, genotype 4
title_full The role of hepatic progenitor cells in predicting response to therapy in Egyptian patients with chronic hepatitis C, genotype 4
title_fullStr The role of hepatic progenitor cells in predicting response to therapy in Egyptian patients with chronic hepatitis C, genotype 4
title_full_unstemmed The role of hepatic progenitor cells in predicting response to therapy in Egyptian patients with chronic hepatitis C, genotype 4
title_short The role of hepatic progenitor cells in predicting response to therapy in Egyptian patients with chronic hepatitis C, genotype 4
title_sort role of hepatic progenitor cells in predicting response to therapy in egyptian patients with chronic hepatitis c, genotype 4
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6531979/
https://www.ncbi.nlm.nih.gov/pubmed/31148968
http://dx.doi.org/10.4314/ahs.v19i1.14
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