Evolution of the hepatitis C virus second envelope protein hypervariable region in chronically infected patients receiving alpha interferon therapy

Citation
Jm. Pawlotsky et al., Evolution of the hepatitis C virus second envelope protein hypervariable region in chronically infected patients receiving alpha interferon therapy, J VIROLOGY, 73(8), 1999, pp. 6490-6499
Citations number
68
Categorie Soggetti
Microbiology
Journal title
JOURNAL OF VIROLOGY
ISSN journal
0022538X → ACNP
Volume
73
Issue
8
Year of publication
1999
Pages
6490 - 6499
Database
ISI
SICI code
0022-538X(199908)73:8<6490:EOTHCV>2.0.ZU;2-#
Abstract
Sustained hepatitis C virus (HCV) RNA clearance is achieved in 8 to 12% of patients with chronic HCV infection treated with alpha interferon (IFN-alph a) at the approved dose of 3 MU three times a week for 6 months and in abou t 25% of those receiving this treatment for 12 months. We used single-stran d conformation polymorphism analysis combined with cloning and sequencing s trategies to characterize the genetic evolution of HCV second envelope gene hypervariable region 1 (HVR1) quasispecies during and after IFN therapy in patients who failed to clear HCV RNA. Sustained HCV RNA clearance was achi eved in 6% of patients. Profound changes in HVR1 quasispecies major variant s were estimated to occur in 70% of the patients during and after therapy. These changes were evolutionary and were characterized by shifts in the vir us population, related to selection and subsequent diversification of minor pretreatment variants. The quasispecies changes appeared to be induced by changes in the host environment likely resulting from the IFN-induced enhan cement and post-IFN attenuation of neutralizing and possibly cytotoxic resp onses against HVR1, The remaining patients had no apparent changes in HVR1 quasispecies major variants, suggesting selection of major pretreatment var iants, but some changes were observed in other genomic regions. We conclude that IFN-alpha administration and withdrawal profoundly alters the nature of circulating HCV quasispecies, owing to profound changes in virus-host in teractions, in patients in whom sustained HCV RNA clearance fails to occur. These changes are associated with profound alterations of the natural outc ome of HCV-related liver disease, raising the hypothesis of a causal relati onship.