Clearance kinetics of hepatitis C virus under different antiviral therapies

Citation
F. Torre et al., Clearance kinetics of hepatitis C virus under different antiviral therapies, J MED VIROL, 64(4), 2001, pp. 455-459
Citations number
17
Categorie Soggetti
Clinical Immunolgy & Infectious Disease",Microbiology
Journal title
JOURNAL OF MEDICAL VIROLOGY
ISSN journal
01466615 → ACNP
Volume
64
Issue
4
Year of publication
2001
Pages
455 - 459
Database
ISI
SICI code
0146-6615(200108)64:4<455:CKOHCV>2.0.ZU;2-A
Abstract
Interferon alpha (IFN) has been the standard treatment for hepatitis C viru s (HCV) infection. Using the kinetic curves of viral clearance, this study compared three treatment regimes based on IFN alone or in combination with Amantadine or Ribavirin to determine the mechanisms of action and the most suitable way to use these drugs. The early clearance kinetics of HCV were s tudied in 22 patients with chronic hepatitis C under different antiviral tr eatments: IFN 3 MU daily (7 pts); IFN 3 MU daily plus Amantadine 200 mg (7 pts); and IFN 3 MU daily plus Ribavirin 1-1.2 gr (8 pts), for 6 months. HCV -RNA was assessed qualitatively and quantitatively on serial samples. The H CV-RNA decay curves suggested a different behaviour of viral clearance indu ced by the three treatments. While no significant differences were present in the first 6 hours, between 6 to 12 hours Ribavirin induced a rapid decli ne in the viral load. Amantadine seemed to accelerate it in the third phase (12 to 30 hours) and to provoke a more pronounced viral decline when compa red to IFN alone (P<0.05) or to IFN plus Ribavirin (P<0.025) (baseline to 3 0 hours). Thus, while IFN remains the principal antiviral drug, Amantadine upholds the viral decline. Ribavirin, although synergistic with IFN, does n ot seem to improve the IFN effect during the earliest phase of Treatment bu t probably supports the effects of IFN later on. A new dynamic approach to HCV treatment can therefore be developed. J. Med. Virol. 64:455-459, 2001. (C) 2001 Wiley-Liss, Inc.