- 作者: Horng-yunn Dou; Jaw-Ching Wu; Wei-li Peng; Chungming Chang; Wei-Kuang Chi; Yi-Ding Chu; Cheng-po Hu
- 作者服務機構: a Department of Medical Research, Veterans General Hospital-Taipei, ; b Institute of Microbiology and Immunology,National Yang-Ming University, c Department of Medicine, Veterans General Hospital-Taipei, ; d National Health Research Institute, ; e -Process Development Division,Development Center for Biotechnology,Taipei, Taiwan, ROC
- 中文摘要: --
- 英文摘要: 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-prolif-erative response and the TCR Vβ 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 Vβ7 gene was utilized more frequently in T cells recognizing HBcAg during remission, while TCR Vβ1 and Vβ2 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 Vβ 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.
- 中文關鍵字: --
- 英文關鍵字: T cell receptor ; Vβ gene usage ; Immune response ; Chronic HBV infection