Evaluation of IFNalpha bioavailability by MxA mRNA in HCV patients

J Immunol Methods. 2002 Apr 1;262(1-2):187-90. doi: 10.1016/s0022-1759(02)00008-x.

Abstract

Previously, we have reported the development of a new quantitative-competitive polymerase chain reaction (qc-PCR) method to evaluate interferon-beta (IFNbeta) bioavailability in multiple sclerosis (MS) patients, by measuring mRNA of mixovirus resistance protein A (MxA). Here we show that our assay is also able to assess IFNalpha bioavailability in hepatitis C virus (HCV) patients treated with different IFNalpha regimens. Indeed, our method was able to detect a slight constitutive expression of MxA mRNA in untreated HCV patients (median=70 fgMxA/pgGAPDH) and a significant induction 12 h after the first IFNalpha administration (median=750 fgMxA/pgGAPDH).

MeSH terms

  • Antiviral Agents / pharmacokinetics*
  • Antiviral Agents / therapeutic use
  • Biological Availability
  • GTP-Binding Proteins*
  • Hepatitis C / blood*
  • Hepatitis C / drug therapy*
  • Humans
  • Interferon-alpha / pharmacokinetics*
  • Interferon-alpha / therapeutic use
  • Leukocytes, Mononuclear / metabolism
  • Myxovirus Resistance Proteins
  • Polymerase Chain Reaction / methods*
  • Proteins / analysis*
  • Proteins / genetics
  • RNA, Messenger / analysis*

Substances

  • Antiviral Agents
  • Interferon-alpha
  • MX1 protein, human
  • Myxovirus Resistance Proteins
  • Proteins
  • RNA, Messenger
  • GTP-Binding Proteins