Immunization with pseudorabies virus harboring Fc domain of IgG makes a contribution to protection of mice from lethal challenge

Vaccine. 2005 May 31;23(29):3775-82. doi: 10.1016/j.vaccine.2005.02.031. Epub 2005 Mar 30.

Abstract

To enhance the efficacy of an inactivated vaccine against pseudorabies virus (PRV), we evaluated the adjuvant properties of Fc domain of IgG. A cell line expressing mouse IgG Fc chimera on its surface was established. We found that when PRV was propagated in the cells expressing the Fc chimera, PRV virion incorporated the Fc. Immunization of BALB/c mice with inactivated PRV harboring Fc, which had been propagated in the cells expressing Fc on its surface, induced higher antibody production against PRV and protected mice more effectively from lethal challenge of virulent strain, comparing to the immunization with normal inactivated virus. Virus harboring Fc has a great potential as a new inactivated vaccine.

MeSH terms

  • Adjuvants, Immunologic / metabolism
  • Animals
  • Antibodies, Viral / blood
  • Cell Line
  • Disease Models, Animal
  • Herpesvirus 1, Suid / immunology
  • Immunoglobulin Fc Fragments / genetics
  • Immunoglobulin Fc Fragments / immunology*
  • Immunoglobulin Fc Fragments / metabolism
  • Immunoglobulin G / immunology
  • Mice
  • Mice, Inbred BALB C
  • Pseudorabies Vaccines / immunology*
  • Swine
  • Vaccines, Inactivated / immunology

Substances

  • Adjuvants, Immunologic
  • Antibodies, Viral
  • Immunoglobulin Fc Fragments
  • Immunoglobulin G
  • Pseudorabies Vaccines
  • Vaccines, Inactivated