Abstract
It is considered that selection pressure exerted by the host immune response during early HCV infection might influence the outcome of that infection particularly as it relates to persistence or clearance of the agent. However, it is unclear whether positive selection pressure plays a role in determining the severity of hepatitis C during the course of persistent HCV infection. To address the evolutionary mechanism by which HCV escapes from the host immune response and to assess the relationship between viral evolution and hepatic inflammation, we determined 57 sequences (3-5 serial samples per patient) from 5 individuals with persistent HCV infection of genotype 1a who were under long-term follow-up ranging from 15.6 to 21.6 years. We applied a novel method to estimate serial alternations of selective pressure against the HCV enveloped region and compared this to fluctuation in transaminase level over time. Positive selection pressure was reduced over time postinfection, as evidenced by a reduction in nonsynonymous substitutions in the later phase of infection. Furthermore, serum transaminase, as a measure of inflammatory necrosis of hepatocytes, was reduced in parallel with decreased positive selection pressure. These results suggest that during persistent HCV infection, the virus faces diminished immune pressure over time, either from mutation to an immune resistant sequence or from immunologic exhaustion, and that this diminished immune attack is reflected in diminished inflammatory activity. This observation may be applicable to other viruses characterized by a slow rate of disease progression.
Original language | English (US) |
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Pages (from-to) | 27-33 |
Number of pages | 7 |
Journal | Virology |
Volume | 361 |
Issue number | 1 |
DOIs | |
State | Published - Apr 25 2007 |
Externally published | Yes |
Bibliographical note
Funding Information:We appreciate Thomas Nagylaki and two reviewers for useful comments. The work was supported by a grant-in-aid from the Ministry of Health, Labour and Welfare of Japan (H16-kanen-3), grants-in-aid for Young Scientists (A) from the Ministry of Education, Culture, Science, Sports of Japan (16689016) and Japan Science and Technology Agency.
Keywords
- Alanine aminotransferase (ALT)
- E2
- Evolution
- HCV
- Immune response
- Persistent infection
- Positive selection
- RNA virus
- Selective pressure
ASJC Scopus subject areas
- Virology