Frequencies of epitope-specific cytotoxic T lymphocytes in active chronic viral hepatitis B infection by using MHC class I peptide tetramers

被引:22
作者
Wu, YZ
Zhang, JB [1 ]
Chen, SY
Chen, A
Wang, L
Li, JY
Zhao, TT
Zou, LY
Tang, Y
Tingrong, L
Wang, F
机构
[1] Third Mil Med Univ, Inst Immunol, PLA, Chongqing 400038, Peoples R China
[2] Hosp Infect Dis Chongqing, Chongqing, Peoples R China
[3] Third Mil Med Univ, SW Hosp, Dept Infect Dis, Chongqing, Peoples R China
关键词
epitope; cytotoxic T lymphocyte; multiple regression analysis; hepatitis B virus; tetramers;
D O I
10.1016/j.imlet.2004.01.002
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Hepatitis B virus (HBV)-specific cytotoxic T lymphocytes (CTLs) are thought to play key roles in viral control and liver damage. We have used HLA-A*02 tetramer complex to human HBV core 18-27 (Tc 18-27), envelope 183-191 (Te 183-191), envelope 335-343 (Te 335-343), and polymerase 575-583 (Tp 575-583) epitopes to characterize HLA class I-restricted CD8+ T cells in active chronic HBV infection. The frequencies of specific epitopes circulating tetramer+ cells were determined in whole-blood samples by analysis of flow cytometry. The correlation of HBV epitope-specific CTL, between viral replication and liver damage, was analyzed by multiple regression. Our data shown that HBV-specific CD8+ T cells can be easily detected in peripheral blood of active chronic HBV infections. No significant correlation was found between either the frequency of HBV-specific CD8+ T cells and the viral load, or the frequency of HBV-specific CD8+ T cells and the levels of alanine transaminase. These results suggest that the existence of epitope-specific HBV CTLs are not directly correlated to hepatocyte injury, and the frequencies of HBV-specific T cells are not determinant of immune-mediated protection in chronic HBV infection. (C) 2004 Elsevier B.V. All rights reserved.
引用
收藏
页码:253 / 258
页数:6
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