The influences of antiviral therapy on T-cell function in adult patients with chronic hepatitis B

Author:

Harkisoen Soeradj1,Kroon Steven1,van Erpecum Karel J2,Hoepelman Andy IM1,Baarle Debbie van34,Arends Joop E13

Affiliation:

1. Department of Internal Medicine & Infectious diseases, University Medical Center Utrecht, Utrecht, The Netherlands

2. Department of Gastroenterology & Hepatology, University Medical Center Utrecht, Utrecht, The Netherlands

3. Department of Immunology, Laboratory for Translational Immunology (LTI), University Medical Center Utrecht, Utrecht, The Netherlands

4. Centre for Infectious Disease Control, National Institute for Public Health & the Environment (RIVM), Bilthoven, The Netherlands

Abstract

ABSTRACT  T cells play an important role in the clearance of acute infection and control of hepatitis B virus (HBV) infection during the chronic phase. Chronic HBV is characterized by a weak and limited T-cell response. Several hypotheses, such as presence of Tregs or occurrence of T-cell exhaustion have been proposed to explain these observations. The two registered classes of anti-HBV drugs: pegylated-IFN-α (PEG-IFN-α) and nucleos(t)ide analogs (NUCs) have, next to their antiviral effect, also an immunomodulatory effect. Although NUCs have no direct immunomodulatory effects, they may indirectly positively affect the T-cell response through their viral suppressive action. In this review, effects of both PEG-IFN-α and NUC therapy will be discussed with regard to the cellular immune response against HBV.

Publisher

Future Medicine Ltd

Subject

Virology

Reference63 articles.

1. World Health Organization. World Hepatitis Day 2012. www.who.int/csr/disease/hepatitis/world_hepatitis_day/en/.

2. World Health Organization. Hepatitis B facts sheet. www.who.int/mediacentre/factsheets/fs204/en/.

3. Dynamic changes of cytotoxic T lymphocytes (CTLs), natural killer (NK) cells, and natural killer T (NKT) cells in patients with acute hepatitis B infection

4. New insights into how HBV manipulates the innate immune response to establish acute and persistent infection

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