Host genetic determinants of spontaneous hepatitis C clearance

Author:

Rauch Andri1,Gaudieri Silvana23,Thio Chloe4,Bochud Pierre-Yves5

Affiliation:

1. University Clinic of Infectious Diseases, University Hospital Bern & University of Bern, Inselspital PKT2B, 3010 Bern, Switzerland.

2. Royal Perth Hospital and Murdoch University, Perth, Australia

3. University of Western Australia, Perth, Australia

4. Johns Hopkins University, MD, USA

5. University Hospital & University of Lausanne, Lausanne, Switzerland

Abstract

Acute infection with the hepatitis C virus (HCV) induces a wide range of innate and adaptive immune responses. A total of 20–50% of acutely HCV-infected individuals permanently control the virus, referred to as ‘spontaneous hepatitis C clearance’, while the infection progresses to chronic hepatitis C in the majority of cases. Numerous studies have examined host genetic determinants of hepatitis C infection outcome and revealed the influence of genetic polymorphisms of human leukocyte antigens, killer immunoglobulin-like receptors, chemokines, interleukins and interferon-stimulated genes on spontaneous hepatitis C clearance. However, most genetic associations were not confirmed in independent cohorts, revealed opposing results in diverse populations or were limited by varying definitions of hepatitis C outcomes or small sample size. Coordinated efforts are needed in the search for key genetic determinants of spontaneous hepatitis C clearance that include well-conducted candidate genetic and genome-wide association studies, direct sequencing and follow-up functional studies.

Publisher

Future Medicine Ltd

Subject

Pharmacology,Genetics,Molecular Medicine

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