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 in | BioMed research international Vol. 2010; no. 2010; pp. 1 - 7 |
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Main Authors | , , , , , |
Format | Journal Article |
Language | English |
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Cairo, Egypt
Hindawi Publishing Corporation
01.01.2010
Dar al -Nasr -al-Llktruni Hindawi Limited |
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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. |
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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 |
AuthorAffiliation_xml | – name: Department of Hepatology, First Hospital, Jilin University, Changchun 130021, China |
Author_xml | – sequence: 1 fullname: Feng, Xiang-Wei – sequence: 2 fullname: Zhang, Hong – sequence: 3 fullname: Jin, Qing-Long – sequence: 4 fullname: Jiang, Yanfang – sequence: 5 fullname: Li, Wan-Yu – sequence: 6 fullname: Niu, Jun-Qi |
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CitedBy_id | crossref_primary_10_17941_agd_676970 crossref_primary_10_1007_s11655_013_1433_7 crossref_primary_10_1016_j_clinre_2020_07_023 crossref_primary_10_3748_wjg_v21_i41_11522 crossref_primary_10_1093_carcin_bgr319 crossref_primary_10_1177_147323001204000131 crossref_primary_10_4236_ym_2017_12008 crossref_primary_10_12659_MSM_899725 |
Cites_doi | 10.1002/jmv.21340 10.1002/hep.21282 10.1155/2009/289068 10.1016/S0016-5085(97)70235-X 10.1016/j.bbrc.2008.12.114 10.1128/JVI.79.21.13412-13420.2005 10.4049/jimmunol.172.12.7432 10.1016/S1473-3099(07)70289-X 10.1084/jem.20060772 10.1002/ptr.2844 10.1099/vir.0.81920-0 10.1002/jmv.20194 10.1084/jem.20011145 10.1111/j.1478-3231.2009.01991.x 10.1086/429492 10.1002/hep.20649 10.4049/jimmunol.164.12.6480 10.1006/clim.2001.5018 10.1155/2009/930268 10.1002/hep.510250438 10.1016/j.jhep.2005.01.038 10.1186/1471-2334-8-123 10.1158/1078-0432.CCR-06-0154 10.1189/jlb.1006622 10.1007/s005350170057 10.1007/s10067-009-1218-8 |
ContentType | Journal Article |
Copyright | Copyright © 2010 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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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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Volume | 2010 |
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