Response of primed human PBMC to synthetic peptides derived from hepatitis B virus envelope proteins: a search for promiscuous epitopes

被引:14
作者
Doh, H
Roh, S
Lee, KW
Kim, K
机构
[1] Ewha Womans Univ, Div Mol Life Sci, Seoul 120750, South Korea
[2] Ewha Womans Univ, Coll Pharm, Seoul 120750, South Korea
[3] Hallym Univ, Coll Med, Dept Clin Pathol, Seoul 134701, South Korea
来源
FEMS IMMUNOLOGY AND MEDICAL MICROBIOLOGY | 2003年 / 35卷 / 01期
基金
新加坡国家研究基金会;
关键词
hepatitis B virus; peripheral blood mononuclear cell; T helper epitope;
D O I
10.1016/S0928-8244(02)00461-3
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 [免疫学];
摘要
This investigation was aimed at identifying effective T helper cell epitopes to the hepatitis B virus in humans. A panel of synthetic peptides that represent the hepatitis B virus whole envelope proteins was examined for their capability to stimulate peripheral blood mononuclear cells from human subjects infected with hepatitis B virus naturally. In addition, a large number of subjects were examined and their human leukocyte antigen (HLA) class II allele types were identified to determine whether the helper T cell epitope is specific for a particular HLA allele or 'promiscuous'. The peptides of the amino acid residues 52-67, 110-125, 190-205, and 228-243 appeared to be immunogenic, and particularly, the 52-67 residue was the most promiscuous epitope peptide. These results would contribute to the better understanding of the helper T cell responses to the hepatitis B virus and provide a useful way in designing epitope-based vaccines and future therapeutic strategies. (C) 2003 Federation of European Microbiological Societies. Published by Elsevier Science B.V. All rights reserved.
引用
收藏
页码:77 / 85
页数:9
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