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.
Original language | English (US) |
---|---|
Pages (from-to) | 1819-1837 |
Number of pages | 19 |
Journal | Pharmacogenomics |
Volume | 10 |
Issue number | 11 |
DOIs | |
State | Published - 2009 |
Keywords
- Association studies
- Genetics
- Hepatitis C
- Spontaneous hepatitis C clearance
ASJC Scopus subject areas
- Molecular Medicine
- Genetics
- Pharmacology