CD8T cells;
chronic hepatitis;
hepatitis B virus;
therapeutic vaccine;
immunodominance;
D O I:
10.1016/S0161-5890(01)00082-7
中图分类号:
Q5 [生物化学];
Q7 [分子生物学];
学科分类号:
071010 ;
081704 ;
摘要:
Chronic hepatitis B virus (HBV) infection is a major cause of morbidity and mortality worldwide, yet currently available therapies fail to provide long-term control of viral replication in most patients. Strategies to boost the weak virus-specific T-cell response typically found in patients with chronic hepatitis B have been proposed as a means of terminating persistent HBV infection. The potential problems arising from the stimulation of virus-specific immunity in a disease caused by a non-cytopathic virus, where viral control and liver injury are mediated by the immune system, are discussed. Furthermore, the concept of augmenting the HBV-specific T-cell response, which has previously been focused solely on quantitative issues, is expanded in the light of new findings of qualitative differences in the HBV-specific CD8 cell response. (C) 2001 Elsevier Science Ltd. All rights reserved.
机构:
Univ Virginia, Beirne B Carter Ctr Immunol Res, Charlottesville, VA 22906 USAUniv Virginia, Beirne B Carter Ctr Immunol Res, Charlottesville, VA 22906 USA
Spencer, JV
;
Braciale, TJ
论文数: 0引用数: 0
h-index: 0
机构:
Univ Virginia, Beirne B Carter Ctr Immunol Res, Charlottesville, VA 22906 USAUniv Virginia, Beirne B Carter Ctr Immunol Res, Charlottesville, VA 22906 USA
机构:
Univ Virginia, Beirne B Carter Ctr Immunol Res, Charlottesville, VA 22906 USAUniv Virginia, Beirne B Carter Ctr Immunol Res, Charlottesville, VA 22906 USA
Spencer, JV
;
Braciale, TJ
论文数: 0引用数: 0
h-index: 0
机构:
Univ Virginia, Beirne B Carter Ctr Immunol Res, Charlottesville, VA 22906 USAUniv Virginia, Beirne B Carter Ctr Immunol Res, Charlottesville, VA 22906 USA