Heterogeneity of HBV-Specific CD8+ T-Cell Failure: Implications for Immunotherapy.

Abstract:

:Chronic hepatitis B virus (HBV) infection is a major global health burden affecting around 257 million people worldwide. The consequences of chronic HBV infection include progressive liver damage, liver cirrhosis, and hepatocellular carcinoma. Although current direct antiviral therapies successfully lead to suppression of viral replication and deceleration of liver cirrhosis progression, these treatments are rarely curative and patients often require a life-long therapy. Based on the ability of the immune system to control HBV infection in at least a subset of patients, immunotherapeutic approaches are promising treatment options to achieve HBV cure. In particular, T cell-based therapies are of special interest since CD8+ T cells are not only capable to control HBV infection but also to eliminate HBV-infected cells. However, recent data show that the molecular mechanisms underlying CD8+ T-cell failure in chronic HBV infection depend on the targeted antigen and thus different strategies to improve the HBV-specific CD8+ T-cell response are required. Here, we review the current knowledge about the heterogeneity of impaired HBV-specific T-cell populations and the potential consequences for T cell-based immunotherapeutic approaches in HBV cure.

journal_name

Front Immunol

journal_title

Frontiers in immunology

authors

Heim K,Neumann-Haefelin C,Thimme R,Hofmann M

doi

10.3389/fimmu.2019.02240

subject

Has Abstract

pub_date

2019-09-20 00:00:00

pages

2240

issn

1664-3224

journal_volume

10

pub_type

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