HBcAg-specific IL-21-producing CD4+ T cells are associated with relative viral control in patients with chronic hepatitis B
Autor: | Juanjuan Fu, Li Li, L.-W. Cheng, Xiu-Cheng Pan, X. Feng, M. Liu, X.-Y. Gao, G. Kong |
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Rok vydání: | 2013 |
Předmět: |
Adult
CD4-Positive T-Lymphocytes Male Hepatitis B virus T cell Immunology CD8-Positive T-Lymphocytes medicine.disease_cause Interleukin 21 Interferon-gamma Immune system Hepatitis B Chronic medicine Cytotoxic T cell Humans Lymphocyte Count business.industry Perforin Interleukins General Medicine Hepatitis B medicine.disease Virology Hepatitis B Core Antigens HBcAg medicine.anatomical_structure Female business CD8 |
Zdroj: | Scandinavian journal of immunology. 78(5) |
ISSN: | 1365-3083 |
Popis: | Function exhaustion of specific cytotoxic CD8+ T cell in chronic virus infection partly results from the low levels of CD4 help, but the mechanisms by which CD4 help T cell required to control hepatitis B virus infection are not well understood. In this study, we investigated the role of interleukin-21-producing CD4+ T cell response in viral control of hepatitis B virus infection. HBcAg-specific interleukin-21-producing CD4+ T cells in blood were detected in patients with hepatitis B virus infection. Patients with acute hepatitis B had greater HBcAg-specific interleukin-21-producing CD4+ T cells in blood compared with chronic hepatitis B patients, and there was no statistical significance between immune active chronic hepatitis B patients and inactive healthy carrier patients for these cells, whereas frequencies of these cells negatively correlated with HBV DNA levels but positively correlated with HBc18-27-specific IFN-γ-producing CD8+ T cells. Moreover, interleukin-21 sustained HBc18-27-specific CD8+ T cells in vitro, and interleukin-21 production by HBcAg-specific IL-21-producing CD4+ T cells of acute hepatitis B patients enhanced IFN-γ and perforin expression by CD8+ T cells from chronic hepatitis B patients. Our results demonstrate that HBcAg-specific interleukin-21-producing CD4+ T cell responses might contribute to viral control by sustaining CD8+ T cell antiviral function. |
Databáze: | OpenAIRE |
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