Impact of deranged B cell subsets distribution in the development of HCV-related cirrhosis and HCC in type two diabetes mellitus

Abstract Type II diabetes (T2D) may worsen the course of hepatitis C virus infection with a greater risk of liver cirrhosis (LC) and hepatocellular carcinoma (HCC). In chronic viral infections, the deranged B cell subset signifies uncontrolled disease. The study aimed to verify the relation between...

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Autores principales: Fadwa A. Abdelwahab, Khaled M. Hassanein, Helal F. Hetta, Mohamed O. Abdelmalek, Asmaa M. Zahran, Omnia El-Badawy
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Publicado: Nature Portfolio 2020
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Acceso en línea:https://doaj.org/article/031740f7403a447d81c2d32cc73eaedf
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spelling oai:doaj.org-article:031740f7403a447d81c2d32cc73eaedf2021-12-02T15:10:11ZImpact of deranged B cell subsets distribution in the development of HCV-related cirrhosis and HCC in type two diabetes mellitus10.1038/s41598-020-77416-02045-2322https://doaj.org/article/031740f7403a447d81c2d32cc73eaedf2020-11-01T00:00:00Zhttps://doi.org/10.1038/s41598-020-77416-0https://doaj.org/toc/2045-2322Abstract Type II diabetes (T2D) may worsen the course of hepatitis C virus infection with a greater risk of liver cirrhosis (LC) and hepatocellular carcinoma (HCC). In chronic viral infections, the deranged B cell subset signifies uncontrolled disease. The study aimed to verify the relation between B cell subsets’ distribution and liver disease progression in chronic hepatitis C (CHC) patients with T2D. A total of 67 CHC patients were divided into two groups; 33 non-diabetic and 34 with T2D. Each group was subdivided into CHC-without LC or HCC (N-CHC), CHC-with LC (CHC-LC), and CHC-with HCC (CHC-HCC). Twenty-seven healthy individuals also participated as controls. Flow cytometry was used to analyze CD19+ B cell subsets based on the expression of CD24 and CD38. CD19+CD24hiCD38hi Immature/transitional B cells elevated in diabetic than non-diabetic patients. In diabetic patients, while CD19+CD24+CD38− primarily memory B cells were higher in CHC-N and CHC-HCC groups than LC with a good predictive accuracy of LC, the opposite was observed for CD19+CD24−CD38− new memory B cells. Only in diabetic patients, the CD19+CD24intCD38int naïve mature B cells were high in CHC-HCC patients with good prognostic accuracy of HCC. Merely in diabetic patients, several correlations were observed between B cell subsets and liver function. Immature/transitional B cells increase remarkably in diabetic CHCpatients and might have a role in liver disease progression. Memory and Naïve B cells are good potential predictors of LC and HCCin diabetic CHCpatients, respectively. Further studies are needed to investigate the role of the CD19+CD24−CD38− new memory B cells in disease progression in CHC patients.Fadwa A. AbdelwahabKhaled M. HassaneinHelal F. HettaMohamed O. AbdelmalekAsmaa M. ZahranOmnia El-BadawyNature PortfolioarticleMedicineRScienceQENScientific Reports, Vol 10, Iss 1, Pp 1-11 (2020)
institution DOAJ
collection DOAJ
language EN
topic Medicine
R
Science
Q
spellingShingle Medicine
R
Science
Q
Fadwa A. Abdelwahab
Khaled M. Hassanein
Helal F. Hetta
Mohamed O. Abdelmalek
Asmaa M. Zahran
Omnia El-Badawy
Impact of deranged B cell subsets distribution in the development of HCV-related cirrhosis and HCC in type two diabetes mellitus
description Abstract Type II diabetes (T2D) may worsen the course of hepatitis C virus infection with a greater risk of liver cirrhosis (LC) and hepatocellular carcinoma (HCC). In chronic viral infections, the deranged B cell subset signifies uncontrolled disease. The study aimed to verify the relation between B cell subsets’ distribution and liver disease progression in chronic hepatitis C (CHC) patients with T2D. A total of 67 CHC patients were divided into two groups; 33 non-diabetic and 34 with T2D. Each group was subdivided into CHC-without LC or HCC (N-CHC), CHC-with LC (CHC-LC), and CHC-with HCC (CHC-HCC). Twenty-seven healthy individuals also participated as controls. Flow cytometry was used to analyze CD19+ B cell subsets based on the expression of CD24 and CD38. CD19+CD24hiCD38hi Immature/transitional B cells elevated in diabetic than non-diabetic patients. In diabetic patients, while CD19+CD24+CD38− primarily memory B cells were higher in CHC-N and CHC-HCC groups than LC with a good predictive accuracy of LC, the opposite was observed for CD19+CD24−CD38− new memory B cells. Only in diabetic patients, the CD19+CD24intCD38int naïve mature B cells were high in CHC-HCC patients with good prognostic accuracy of HCC. Merely in diabetic patients, several correlations were observed between B cell subsets and liver function. Immature/transitional B cells increase remarkably in diabetic CHCpatients and might have a role in liver disease progression. Memory and Naïve B cells are good potential predictors of LC and HCCin diabetic CHCpatients, respectively. Further studies are needed to investigate the role of the CD19+CD24−CD38− new memory B cells in disease progression in CHC patients.
format article
author Fadwa A. Abdelwahab
Khaled M. Hassanein
Helal F. Hetta
Mohamed O. Abdelmalek
Asmaa M. Zahran
Omnia El-Badawy
author_facet Fadwa A. Abdelwahab
Khaled M. Hassanein
Helal F. Hetta
Mohamed O. Abdelmalek
Asmaa M. Zahran
Omnia El-Badawy
author_sort Fadwa A. Abdelwahab
title Impact of deranged B cell subsets distribution in the development of HCV-related cirrhosis and HCC in type two diabetes mellitus
title_short Impact of deranged B cell subsets distribution in the development of HCV-related cirrhosis and HCC in type two diabetes mellitus
title_full Impact of deranged B cell subsets distribution in the development of HCV-related cirrhosis and HCC in type two diabetes mellitus
title_fullStr Impact of deranged B cell subsets distribution in the development of HCV-related cirrhosis and HCC in type two diabetes mellitus
title_full_unstemmed Impact of deranged B cell subsets distribution in the development of HCV-related cirrhosis and HCC in type two diabetes mellitus
title_sort impact of deranged b cell subsets distribution in the development of hcv-related cirrhosis and hcc in type two diabetes mellitus
publisher Nature Portfolio
publishDate 2020
url https://doaj.org/article/031740f7403a447d81c2d32cc73eaedf
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