Analysis of T cell receptor Vβ gene usage during the course of disease in patients with chronic hepatitis B

被引:8
作者
Dou, HY
Wu, JC
Peng, WL
Chang, CM
Chi, WK
Chu, YD
Hu, CP [1 ]
机构
[1] Vet Gen Hosp, Dept Med Res, Taipei 112, Taiwan
[2] Natl Yang Ming Univ, Inst Microbiol & Immunol, Taipei 112, Taiwan
[3] Vet Gen Hosp, Dept Med, Taipei, Taiwan
[4] Natl Hlth Res Inst, Taipei, Taiwan
[5] Dev Ctr Biotechnol, Proc Dev Div, Taipei, Taiwan
关键词
T cell receptor; V-beta gene usage; immune response; chronic HBV infection;
D O I
10.1007/BF02255931
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The T cell receptor (TCR) is a heterodimeric molecule expressed on the surface of T cells and recognizes foreign peptides presented by the major histocompatibility complex on the surface of antigen-presenting cells or virus-infected cells. Analysis of TCR usage by T cells which recognize hepatitis B virus (HBV) provides further insight into the participation of T cell populations during the course of disease, In this study, we examined the T-cell-proliferative response and the TCR V beta gene usage of peripheral blood mononuclear cells in 3 patients with clinical evidence typical of chronic hepatitis B. All 3 patients had significant T-cell proliferative responses against HBV core antigen (HBcAg) during the remission stage, while no responses were detected during the acute exacerbation stage. In addition, the TCR V-beta 7 gene was utilized more frequently in T cells recognizing HBcAg during remission, while TCR V-beta 1 and V-beta 2 were utilized at a higher percentage during acute exacerbation. On the contrary, the T cell proliferative response against HBV surface antigen was undetectable and no specific V beta gene was utilized more frequently by all 3 patients, regardless of disease state. Our longitudinal studies, although based on a small sample of patients, demonstrate that the population of HBcAg-activated T cells alters during the course of disease in chronic hepatitis B patients.
引用
收藏
页码:428 / 434
页数:7
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