An immunodominant HLA-A*1101-restricted CD8+ T-cell response targeting hepatitis B surface antigen in chronic hepatitis B patients

被引:6
|
作者
Chen, Xiaoling [1 ,2 ]
Wang, Wenbo [1 ,2 ]
Wang, Shufeng [1 ,2 ]
Meng, Gang [3 ]
Zhang, Mengjun [4 ]
Ni, Bing [1 ,2 ]
Wu, Yuzhang [1 ,2 ]
Wang, Li [1 ,2 ]
机构
[1] Third Mil Med Univ, Dept Immunol, Chongqing 400038, Peoples R China
[2] PLA, Inst Immunol, Chongqing 400038, Peoples R China
[3] Third Mil Med Univ, Southwest Hosp, Dept Pathol, Chongqing 400038, Peoples R China
[4] Third Mil Med Univ, Fac Lab Med, Dept Analyt Chem, Chongqing 400038, Peoples R China
来源
JOURNAL OF GENERAL VIROLOGY | 2013年 / 94卷
基金
中国国家自然科学基金;
关键词
CHRONIC HBV INFECTION; VIRUS-INFECTION; LYMPHOCYTE RESPONSES; VIRAL-HEPATITIS; CLASS-I; HLA; EPITOPES; PROTEINS; POLYMORPHISM; POPULATION;
D O I
10.1099/vir.0.052167-0
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Hepatitis B virus (HBV) infection is a worldwide public health problem. HBV-specific CD8(+) CTLs are vital for viral clearance. Identification of immunodominant CTL epitopes from HBV-associated antigens is necessary for therapeutic vaccine development. We showed that the HLA-A*1101 allele is one of the most common alleles in both healthy individuals and chronic hepatitis B (CHB) patients in the Chongqing area, China. However, less than 10% of epitopes of HBV-associated antigens have been identified in an HLA-A*1101 context. Here, we describe an immunodominant CD8(+) T-cell response targeting a hepatitis B surface antigen determinant (HBs(295-304)) restricted by HLA-A*1101 in both healthy individuals and CHB patients. Moreover, HBs(295-304) is more immunogenic for CTL induction than a known naturally HLA-A*1101-processed epitope from hepatitis B core antigen (HBc(88-96)). Therefore, the newly identified epitope, HBs(295-304), will benefit the development of immunotherapeutic approaches for HBV infection.
引用
收藏
页码:2717 / 2723
页数:7
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