An alpaca nanobody inhibits hepatitis C virus entry and cell-to-cell transmission

Hepatology. 2013 Sep;58(3):932-9. doi: 10.1002/hep.26430. Epub 2013 Jul 30.

Abstract

Severe liver disease caused by chronic hepatitis C virus is the major indication for liver transplantation. Despite recent advances in antiviral therapy, drug toxicity and unwanted side effects render effective treatment in liver-transplanted patients a challenging task. Virus-specific therapeutic antibodies are generally safe and well-tolerated, but their potential in preventing and treating hepatitis C virus (HCV) infection has not yet been realized due to a variety of issues, not least high production costs and virus variability. Heavy-chain antibodies or nanobodies, produced by camelids, represent an exciting antiviral approach; they can target novel highly conserved epitopes that are inaccessible to normal antibodies, and they are also easy to manipulate and produce. We isolated four distinct nanobodies from a phage-display library generated from an alpaca immunized with HCV E2 glycoprotein. One of them, nanobody D03, recognized a novel epitope overlapping with the epitopes of several broadly neutralizing human monoclonal antibodies. Its crystal structure revealed a long complementarity determining region (CD3) folding over part of the framework that, in conventional antibodies, forms the interface between heavy and light chain. D03 neutralized a panel of retroviral particles pseudotyped with HCV glycoproteins from six genotypes and authentic cell culture-derived particles by interfering with the E2-CD81 interaction. In contrast to some of the most broadly neutralizing human anti-E2 monoclonal antibodies, D03 efficiently inhibited HCV cell-to-cell transmission.

Conclusion: This is the first description of a potent and broadly neutralizing HCV-specific nanobody representing a significant advance that will lead to future development of novel entry inhibitors for the treatment and prevention of HCV infection and help our understanding of HCV cell-to-cell transmission.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Sequence
  • Animals
  • Camelids, New World / immunology*
  • Cell Communication / drug effects*
  • Cell Line, Tumor
  • Cells, Cultured
  • Epitope Mapping
  • Epitopes / genetics
  • Epitopes / immunology
  • Genotype
  • Hepacivirus / immunology*
  • Hepacivirus / pathogenicity
  • Hepatitis C / prevention & control
  • Hepatitis C / transmission
  • Humans
  • Liver / drug effects
  • Liver / pathology
  • Liver / virology
  • Molecular Sequence Data
  • Single-Domain Antibodies / chemistry
  • Single-Domain Antibodies / immunology*
  • Single-Domain Antibodies / pharmacology*
  • Viral Envelope Proteins / immunology*
  • Virus Internalization / drug effects*

Substances

  • Epitopes
  • Single-Domain Antibodies
  • Viral Envelope Proteins
  • glycoprotein E2, Hepatitis C virus