Comparison of HCV Core and CoreE1E2 Virus-Like Particles Generated by Stably Transfected Leishmania tarentolae for the Stimulation of Th1 Immune Responses in Mice

Curr Drug Deliv. 2017;14(7):1040-1049. doi: 10.2174/1567201814666170125120917.

Abstract

Background: Virus-like particles (VLPs) could be improved into successful immunogens as well as a potent delivery vehicle, but however, the current expression systems for VLPs production have some limitations.

Method: Recently, we developed a novel strategy to produce two HCV VLPs containing core or coreE1E2 proteins using stably transfected Leishmania tarentolae promastigotes. Then, BALB/c mice were injected by both viral like particles in different immunization strategies such as homologous DNA-, homologous VLP-, and heterologous DNA/ VLP-based immunizations.

Results: TEM microscopy indicated HCV core and HCV coreE1E2 VLP assembly with average size of 30-40 and 40-60 nm after purification, respectively. Our results showed that homologous immunizations with both HCV core or coreE1E2 VLPs significantly induced anti-core or anti- coreE1E2 antibody responses, respectively as well as secretion of IFN-γ cytokine as compared to other strategies. Moreover, DNA-prime/VLP-boost regimens significantly elicited higher levels of IFN-γ and antibody responses in comparison with homologous DNA/DNA regimens. The groups immunized with homologous or heterologous coreE1E2 VLPs showed markedly higher immune responses as compared to groups immunized with core VLP regimens against coreE1E2 protein.

Conclusion: The crude HCV VLPs generated by Leishmania expression system could elicit a Th1- type response as a promising vaccine candidate against HCV infections.

Keywords: Core; CoreE1E2; DNA; HCV; Leishmania tarentolae; Viral like particle (VLP).

Publication types

  • Comparative Study

MeSH terms

  • Animals
  • Female
  • HEK293 Cells
  • Hepacivirus*
  • Humans
  • Immunization
  • Immunoglobulin G / blood
  • Interferon-gamma / blood
  • Interleukin-4 / blood
  • Leishmania / genetics*
  • Leishmania / metabolism
  • Mice, Inbred BALB C
  • Th1 Cells / immunology
  • Transfection
  • Vaccines, Virus-Like Particle / administration & dosage*
  • Viral Core Proteins / genetics*
  • Viral Core Proteins / metabolism

Substances

  • Immunoglobulin G
  • Vaccines, Virus-Like Particle
  • Viral Core Proteins
  • Interleukin-4
  • Interferon-gamma