The molecular basis of the failed immune response in chronic HBV: Therapeutic implications

被引:140
作者
Maini, Mala K. [1 ]
Schurich, Anna [1 ]
机构
[1] UCL, Dept Immunol & Mol Pathol, London WC1E 6BT, England
基金
英国医学研究理事会;
关键词
CD8 T cell exhaustion; Chronic hepatitis B virus infection; Immunotherapy; HEPATITIS-B-VIRUS; CD8(+) T-CELLS; GROWTH-FACTOR-BETA; LAMIVUDINE TREATMENT; ENDOTHELIAL-CELLS; LIVER-DAMAGE; IN-VIVO; INFECTION; DELETION; ANTIGEN;
D O I
10.1016/j.jhep.2009.12.017
中图分类号
R57 [消化系及腹部疾病];
学科分类号
100201 [内科学];
摘要
There is a pressing need to develop new immunotherapeutic interventions in chronic hepatitis B virus (HBV) infection in order to limit the high costs and risks of toxicity or viral resistance associated with maintenance antiviral treatment. Here we review recent advances in our understanding of the molecular defects underlying the profound T cell depletion characteristic of these patients. We propose that T cells are driven to apoptosis by the combination of persistent, high antigen load and excessive inhibitory signals encountered in the hepatic microenvironment. The feasibility of boosting sustained antiviral control by targeted reversal of key tolerising mechanisms is discussed. (c) 2010 European Association for the Study of the Liver. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:616 / 619
页数:4
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