Enhancing the utility of a prM/E-expressing chimeric vaccine for Japanese encephalitis by addition of the JEV NS1 gene

Vaccine. 2011 Oct 6;29(43):7444-55. doi: 10.1016/j.vaccine.2011.07.058. Epub 2011 Jul 26.

Abstract

Recently, we demonstrated that a single-cycle West Nile virus (WNV) named RepliVAX WN could be used to produce a chimeric Japanese encephalitis (JE) vaccine (RepliVAX JE) by replacing the WNV prM/E genes with those of JEV. Here, we tested if replacement of WNV NS1 gene in RepliVAX JE with that of JEV (producing TripliVAX JE) could produce a superior vaccine. TripliVAX JE elicited higher anti-E immunity and displayed better efficacy in mice than RepliVAX JE. Furthermore, TripliVAX JE displayed reduced immune interference caused by pre-existing anti-NS1 immunity. Thus, we propose prM/E/NS1 chimerization as a new strategy for flavivirus vaccine development.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antibodies, Viral / immunology
  • Base Sequence
  • Chlorocebus aethiops
  • Cricetinae
  • Encephalitis Virus, Japanese / immunology*
  • Encephalitis, Japanese / immunology*
  • Encephalitis, Japanese / prevention & control
  • Japanese Encephalitis Vaccines / immunology*
  • Mice
  • Neutralization Tests
  • Sequence Analysis, RNA
  • Vaccination
  • Vero Cells
  • Viral Nonstructural Proteins / genetics
  • Viral Nonstructural Proteins / immunology*
  • Viral Proteins / immunology

Substances

  • Antibodies, Viral
  • Japanese Encephalitis Vaccines
  • NS1 protein, Flavivirus
  • Viral Nonstructural Proteins
  • Viral Proteins