Interleukin 28B genetic polymorphism and hepatitis B virus infection

doi:10.3748/wjg.v20.i34.12026

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World Journal of Gastroenterology

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1007-9327

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World J Gastroenterol. Sep 14, 2014; 20(34): 12026-12030
Published online Sep 14, 2014. doi: 10.3748/wjg.v20.i34.12026

Interleukin 28B genetic polymorphism and hepatitis B virus infection

Toru Takahashi

Toru Takahashi, Division of Gastroenterology and Hepatology, Uonuma Hospital, Ojiyashi, Niigata 947-0028, Japan

Author contributions: Takahashi T solely contributed to this paper.

Correspondence to: Toru Takahashi, MD, PhD, Director, Division of Gastroenterology and Hepatology, Uonuma Hospital, 4-1-38 Jonai, Ojiyashi, Niigata 947-0028, Japan. torutoru@uonumahosp.jp

Telephone: +81-25-8832870 Fax: +81-25-8834789

Received: October 27, 2013
Revised: January 24, 2014
Accepted: April 8, 2014
Published online: September 14, 2014
Processing time: 326 Days and 3.4 Hours

Abstract

Interleukin (IL) 28B genetic polymorphism is significantly associated with the sustained virological response rate in patients with chronic hepatitis C treated with pegylated interferon-α (PEG-IFN) plus ribavirin and with spontaneous hepatitis C virus clearance. However, a consensus on the relationship between IL28B genetic polymorphism and the favorable outcome of chronic hepatitis B virus infection defined by hepatitis B e antigen seroconversion, and/or hepatitis B surface antigen seroclearance in patients treated with interferon or PEG-IFN has not been reached. Several reports failed to show a positive association, while some studies demonstrated a positive association in certain subject settings. More prospective studies including large cohorts are needed to determine the possible association between IL28B genetic polymorphism and the outcome of interferon or PEG-IFN treatment for chronic hepatitis B.

Keywords: Interleukin 28B; Polymorphism; Hepatitis B virus; Interferon; Pegylated interferon

Core tip: An association between interleukin (IL) 28B genetic polymorphism and sustained virological response rate in patients with chronic hepatitis C treated with pegylated interferon-α and ribavirin or spontaneous hepatitis C virus clearance has been established. However, the association between IL28B genetic polymorphism and hepatitis B virus infection remains unclear. We discuss this topic and summarize the available clinical data.