Immunologic Characterization of Posthepatitis Cirrhosis Caused by HBV and HCV Infection

No specific treatment can reverse the liver injury in cirrhosis. This study aims to characterize immune status and correlations between cirrhosis induced by HBV and HCV. Phenotypes of peripheral blood lymphocyte subsets (T, NK, regulatory T cells) and Th cytokine secretion were analyzed using flow c...

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Published inBioMed research international Vol. 2010; no. 2010; pp. 1 - 7
Main Authors Feng, Xiang-Wei, Zhang, Hong, Jin, Qing-Long, Jiang, Yanfang, Li, Wan-Yu, Niu, Jun-Qi
Format Journal Article
LanguageEnglish
Published Cairo, Egypt Hindawi Publishing Corporation 01.01.2010
Dar al -Nasr -al-Llktruni
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Abstract No specific treatment can reverse the liver injury in cirrhosis. This study aims to characterize immune status and correlations between cirrhosis induced by HBV and HCV. Phenotypes of peripheral blood lymphocyte subsets (T, NK, regulatory T cells) and Th cytokine secretion were analyzed using flow cytometry in 42 HBV-cirrhotic and 40 HCV-cirrhotic patients. Cirrhotic patients had a lower proportion of CD3+CD8+T cells and NK cells, while the proportion of CD3+CD4+T cells and Treg cells were higher than those of healthy controls. The levels of Th2 cytokine (IL-6) in cirrhotic patients were increased, while only the Th1 cytokine (IFN-γ) increased in HBV-cirrhotic patients. These findings show that there is no difference between the cirrhotic groups except in the IFN-γ level. In cirrhosis, defects in innate, adaptive immune cells are likely regardless of which virus is involved. A cytokine imbalance may play a role in the development of posthepatitic cirrhosis.
AbstractList No specific treatment can reverse the liver injury in cirrhosis. This study aims to characterize immune status and correlations between cirrhosis induced by HBV and HCV. Phenotypes of peripheral blood lymphocyte subsets (T, NK, regulatory T cells) and Th cytokine secretion were analyzed using flow cytometry in 42 HBV-cirrhotic and 40 HCV-cirrhotic patients. Cirrhotic patients had a lower proportion of CD3 + CD8 + T cells and NK cells, while the proportion of CD3 + CD4 + T cells and Treg cells were higher than those of healthy controls. The levels of Th2 cytokine (IL-6) in cirrhotic patients were increased, while only the Th1 cytokine (IFN- γ ) increased in HBV-cirrhotic patients. These findings show that there is no difference between the cirrhotic groups except in the IFN- γ level. In cirrhosis, defects in innate, adaptive immune cells are likely regardless of which virus is involved. A cytokine imbalance may play a role in the development of posthepatitic cirrhosis.
No specific treatment can reverse the liver injury in cirrhosis. This study aims to characterize immune status and correlations between cirrhosis induced by HBV and HCV. Phenotypes of peripheral blood lymphocyte subsets (T, NK, regulatory T cells) and Th cytokine secretion were analyzed using flow cytometry in 42 HBV-cirrhotic and 40 HCV-cirrhotic patients. Cirrhotic patients had a lower proportion of CD3+CD8+T cells and NK cells, while the proportion of CD3+CD4+T cells and Treg cells were higher than those of healthy controls. The levels of Th2 cytokine (IL-6) in cirrhotic patients were increased, while only the Th1 cytokine (IFN-γ) increased in HBV-cirrhotic patients. These findings show that there is no difference between the cirrhotic groups except in the IFN-γ level. In cirrhosis, defects in innate, adaptive immune cells are likely regardless of which virus is involved. A cytokine imbalance may play a role in the development of posthepatitic cirrhosis.
No specific treatment can reverse the liver injury in cirrhosis. This study aims to characterize immune status and correlations between cirrhosis induced by HBV and HCV. Phenotypes of peripheral blood lymphocyte subsets (T, NK, regulatory T cells) and Th cytokine secretion were analyzed using flow cytometry in 42 HBV-cirrhotic and 40 HCV-cirrhotic patients. Cirrhotic patients had a lower proportion of CD3+CD8+T cells and NK cells, while the proportion of CD3+CD4+T cells and Treg cells were higher than those of healthy controls. The levels of Th2 cytokine (IL-6) in cirrhotic patients were increased, while only the Th1 cytokine (IFN- g) increased in HBV-cirrhotic patients. These findings show that there is no difference between the cirrhotic groups except in the IFN- g level. In cirrhosis, defects in innate, adaptive immune cells are likely regardless of which virus is involved. A cytokine imbalance may play a role in the development of posthepatitic cirrhosis.
No specific treatment can reverse the liver injury in cirrhosis. This study aims to characterize immune status and correlations between cirrhosis induced by HBV and HCV. Phenotypes of peripheral blood lymphocyte subsets (T, NK, regulatory T cells) and Th cytokine secretion were analyzed using flow cytometry in 42 HBV-cirrhotic and 40 HCV-cirrhotic patients. Cirrhotic patients had a lower proportion of CD3(+)CD8(+)T cells and NK cells, while the proportion of CD3(+)CD4(+)T cells and Treg cells were higher than those of healthy controls. The levels of Th2 cytokine (IL-6) in cirrhotic patients were increased, while only the Th1 cytokine (IFN-gamma) increased in HBV-cirrhotic patients. These findings show that there is no difference between the cirrhotic groups except in the IFN-gamma level. In cirrhosis, defects in innate, adaptive immune cells are likely regardless of which virus is involved. A cytokine imbalance may play a role in the development of posthepatitic cirrhosis.
Author Zhang, Hong
Jin, Qing-Long
Jiang, Yanfang
Niu, Jun-Qi
Feng, Xiang-Wei
Li, Wan-Yu
AuthorAffiliation Department of Hepatology, First Hospital, Jilin University, Changchun 130021, China
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2015 INIST-CNRS
Copyright © 2010 Wan-Yu Li et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
Copyright © 2010 Wan-Yu Li et al. 2010
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Issue 2010
Keywords Infection
Characterization
Viral hepatitis B
Cirrhosis
Viral disease
Digestive diseases
Hepatic disease
Viral hepatitis C
Language English
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SubjectTerms Adult
Aged
Biological and medical sciences
Biomedical research
Blood
CD4 Antigens
CD4-CD8 Ratio
Deoxyribonucleic acid
Disease
DNA
Female
Forkhead Transcription Factors
Gastroenterology. Liver. Pancreas. Abdomen
Hepatitis B - complications
Hepatitis B virus
Hepatitis C - complications
Hepatitis C virus
Hepatology
Human viral diseases
Humans
Immune system
Infections
Infectious diseases
Interferon-gamma
Interleukins
Liver cirrhosis
Liver Cirrhosis - complications
Liver Cirrhosis - immunology
Liver Cirrhosis - metabolism
Liver. Biliary tract. Portal circulation. Exocrine pancreas
Lymphocytes
Lymphocytes - immunology
Lymphocytes - metabolism
Male
Medical sciences
Middle Aged
Other diseases. Semiology
Pathogenesis
Tropical diseases
Viral diseases
Viral hepatitis
Viral infections
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Title Immunologic Characterization of Posthepatitis Cirrhosis Caused by HBV and HCV Infection
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https://dx.doi.org/10.1155/2010/138237
https://www.ncbi.nlm.nih.gov/pubmed/20617133
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Volume 2010
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