Role of Some Predominant Host Immunomodulators' Single Nucleotide Polymorphisms in Severity of Hepatitis B Virus and Hepatitis C Virus Infection

Viral Immunol. 2016 Dec;29(10):536-545. doi: 10.1089/vim.2016.0062. Epub 2016 Sep 27.

Abstract

Hepatitis B and C infections can be either acute or chronic. The chronic infection can culminate in liver cirrhosis and hepatocellular carcinoma. Influence of the host genetic makeup on conversion of acute to chronic infection, development of cirrhosis, and hepatocellular carcinoma is an interesting area of research. Variability in different immune system genes may account for such differences in the outcome of infection. This article discusses single nucleotide polymorphisms in different host immunomodulator genes that have been frequently reported to influence the outcome of infection and severity of disease. The genetic variability could be utilized for the prediction of disease outcome and treatment responses.

Keywords: chronic infections; host–virus interactions; susceptibility; treatment.

Publication types

  • Review

MeSH terms

  • Carcinoma, Hepatocellular / immunology*
  • HLA Antigens / genetics
  • HLA Antigens / immunology
  • Hepacivirus / immunology*
  • Hepatitis B virus / immunology*
  • Hepatitis B, Chronic / complications
  • Hepatitis B, Chronic / immunology*
  • Hepatitis C, Chronic / complications
  • Hepatitis C, Chronic / immunology*
  • Humans
  • Immunologic Factors / genetics*
  • Immunologic Factors / immunology
  • Interleukins / genetics
  • Interleukins / immunology
  • Liver Cirrhosis / etiology
  • Liver Cirrhosis / immunology*
  • Liver Neoplasms / immunology*
  • Mannose-Binding Lectin / genetics
  • Mannose-Binding Lectin / immunology
  • Polymorphism, Single Nucleotide
  • Receptor, Interferon alpha-beta / genetics
  • Receptor, Interferon alpha-beta / immunology
  • Receptors, CCR5 / genetics
  • Receptors, CCR5 / immunology
  • Tumor Necrosis Factor-alpha / genetics
  • Tumor Necrosis Factor-alpha / immunology

Substances

  • CCR5 protein, human
  • HLA Antigens
  • IFNAR1 protein, human
  • Immunologic Factors
  • Interleukins
  • MBL2 protein, human
  • Mannose-Binding Lectin
  • Receptors, CCR5
  • Tumor Necrosis Factor-alpha
  • Receptor, Interferon alpha-beta