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  4. Peginterferon α in the treatment of chronic hepatitis B
 
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Peginterferon α in the treatment of chronic hepatitis B

Journal
Expert Opinion on Biological Therapy
Journal Volume
14
Journal Issue
7
Pages
995-1006
Date Issued
2014
Author(s)
TAI-CHUNG TSENG  
JIA-HORNG KAO  
DING-SHINN CHEN  
DOI
10.1517/14712598.2014.907784
URI
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84902159056&doi=10.1517%2f14712598.2014.907784&partnerID=40&md5=4d22ed339963535f13844d831651d32e
https://scholars.lib.ntu.edu.tw/handle/123456789/581985
Abstract
Introduction: Hepatitis B virus (HBV) infection is a global health problem. Peginterferon α (PEG-IFN), which includes PEG-IFN α-2a (Pegasys) and PEG-IFN α-2b (Peg-Intron), can be used to treat patients with chronic hepatitis B (CHB) infection. A finite duration of PEG-IFN therapy may lead to long-term viral suppression. Clinically, it is important to identify super-responders and null-responders to PEG-IFN due to its substantial side effects. Areas covered: From the literature review, it is known that PEG-IFN is more effective for hepatitis B e antigen (HBeAg)-positive patients who have high pre-treatment alanine aminotransferase level, lower HBV DNA level and genotype A (vs genotype D), as well as those with more favourable viral predictors, such as precore stop codon or basal core promoter mutants infections in Asian patients and wild-type virus in Caucasian patients. For HBeAg-positive patients and HBeAg-negative patients with genotype D infection, PEG-IFN therapy could be terminated early at week 12 or 24 in primary non-responders defined by the Hepatitis B surface antigen stopping rules. With regard to host factors, single nucleotide polymorphisms of IL28B do not seem to affect the treatment outcomes in Asian patients, but its role in Caucasian patients remains disputed. Expert opinion: Most of the known predictors need validation by large prospective trials. In addition, we need to identify more baseline predictors for super-responders in order to achieve personalised PEG-IFN treatment for CHB. ? 2014 Informa UK, Ltd.
Subjects
Basal core promoter; Chronic hepatitis B; Genotype; HBsAg; Hepatitis B e antigen; Hepatitis B virus; IL28B; PEG-IFN; Precore stop codon
SDGs

[SDGs]SDG3

Other Subjects
alanine aminotransferase; hepatitis B surface antigen; hepatitis B(e) antigen; host factor; interleukin 28B; peginterferon alpha; peginterferon alpha2a; peginterferon alpha2b; virus DNA; alpha interferon; antivirus agent; hepatitis B surface antigen; hepatitis B(e) antigen; IL28B protein, human; interleukin derivative; macrogol derivative; peginterferon alpha2a; peginterferon alpha2b; recombinant protein; alanine aminotransferase blood level; article; Asian; Caucasian; drug efficacy; genotype; hepatitis B; Hepatitis B virus; history; human; mutant; optimal drug dose; prediction; quantitative analysis; single nucleotide polymorphism; stop codon; treatment duration; treatment outcome; treatment response; genetics; Hepatitis B, Chronic; immunology; prospective study; Antiviral Agents; Genotype; Hepatitis B e Antigens; Hepatitis B Surface Antigens; Hepatitis B virus; Hepatitis B, Chronic; Humans; Interferon-alpha; Interleukins; Polyethylene Glycols; Polymorphism, Single Nucleotide; Prospective Studies; Recombinant Proteins; Treatment Outcome
Publisher
Informa Healthcare
Type
journal article

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