Cutting edge: recombinant Listeria monocytogenes expressing a single immune-dominant peptide confers protective immunity to herpes simplex virus-1 infection

J Immunol. 2007 Apr 15;178(8):4731-5. doi: 10.4049/jimmunol.178.8.4731.

Abstract

The vast majority of the world's population is infected with HSV. Although antiviral therapy can reduce the incidence of reactivation and asymptomatic viral shedding, and limit morbidity and mortality from active disease, it cannot cure infection. Therefore, the development of an effective vaccine is an important global health priority. In this study, we demonstrate that recombinant Listeria monocytogenes (Lm) expressing the H-2K(b) glycoprotein B (gB)(498-505) peptide from HSV-1 triggers a robust CD8 T cell response to this Ag resulting in protective immunity to HSV infection. Following challenge with HSV-1, immune-competent mice primed with recombinant Lm-expressing gB(498-505) Ag were protected from HSV-induced paralysis. Protection was associated with dramatic reductions in recoverable virus, and early expansion of HSV-1-specific CD8 T cells in the regional lymph nodes. Thus, recombinant Lm-expressing Ag from HSV represents a promising new class of vaccines against HSV infection.

Publication types

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

MeSH terms

  • Animals
  • CD8-Positive T-Lymphocytes / immunology
  • Female
  • Herpes Simplex Virus Vaccines / immunology*
  • Herpesvirus 1, Human / immunology*
  • Interferon-gamma / biosynthesis
  • Listeria monocytogenes / genetics*
  • Mice
  • Mice, Inbred C57BL
  • Peptide Fragments / immunology*
  • Vaccines, Synthetic / immunology*
  • Viral Envelope Proteins / genetics
  • Viral Envelope Proteins / immunology*

Substances

  • Herpes Simplex Virus Vaccines
  • Peptide Fragments
  • Vaccines, Synthetic
  • Viral Envelope Proteins
  • glycoprotein B, Simplexvirus
  • Interferon-gamma