Infection of primary human macrophages with hepatitis C virus in vitro: induction of tumour necrosis factor-alpha and interleukin 8

J Gen Virol. 2004 Jan;85(Pt 1):47-59. doi: 10.1099/vir.0.19491-0.

Abstract

Hepatitis C virus (HCV) has been reported to replicate in monocytes/macrophages in infected patients. However, it is unclear whether macrophages are susceptible to infection in vitro and whether such an infection is consequential. Sera from 26 HCV-infected patients were incubated with primary human macrophages collected from healthy donors. Virus negative strand was detected by a Tth enzyme-based strand-specific assay and virus sequences were analysed by single strand conformation polymorphism (SSCP) and sequencing. Concentrations of the cytokines tumour necrosis factor-alpha (TNF-alpha) and interleukin (IL)-1beta, IL-6, IL-8, IL-10 and IL-12p70 were measured in culture supernatants and respective mRNAs were analysed in cell extracts by quantitative RT-PCR. For 15 sera, HCV RNA was detectable in 2- and 3-week cultures from at least one donor. Virus negative strand was detected in 29 % of macrophage samples in this group. In four cases, HCV RNA sequences amplified from macrophages differed from those amplified from sera suggesting evolution during infection. Concentrations of TNF-alpha and IL-8 were found to be significantly higher in supernatants from HCV-infected cultures. In conclusion, these preliminary data suggest that primary human macrophages are susceptible to HCV infection in vitro and this infection is associated with the induction of cytokines TNF-alpha and IL-8.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Cells, Cultured
  • Culture Media, Conditioned / metabolism
  • Cytokines / biosynthesis
  • Cytokines / genetics
  • Hepacivirus / immunology
  • Hepacivirus / pathogenicity*
  • Hepatitis C / immunology
  • Hepatitis C / virology
  • Humans
  • Interleukin-8 / biosynthesis*
  • Macrophages / immunology
  • Macrophages / virology*
  • RNA, Messenger / metabolism
  • RNA, Viral / analysis
  • Reverse Transcriptase Polymerase Chain Reaction
  • Tumor Necrosis Factor-alpha / biosynthesis*

Substances

  • Culture Media, Conditioned
  • Cytokines
  • Interleukin-8
  • RNA, Messenger
  • RNA, Viral
  • Tumor Necrosis Factor-alpha