Virus-like particles vaccine containing Clonorchis sinensis tegumental protein induces partial protection against Clonorchis sinensis infection

Parasit Vectors. 2017 Dec 29;10(1):626. doi: 10.1186/s13071-017-2526-5.

Abstract

Background: Human clonorchiasis, caused by the infection of Clonorchis sinensis, is one of the major health problems in Southeast Asia. However, vaccine efficacy against C. sinensis infection remains largely unknown.

Methods: In this study, for the first time, we generated virus-like particles (VLPs) vaccine containing the C. sinensis tegumental protein 22.3 kDa (CsTP 22.3) and the influenza matrix protein (M1) as a core protein, and investigated the vaccine efficacy in Sprague-Dawley rats.

Results: Intranasal immunization of VLPs vaccine induced C. sinensis-specific IgG, IgG2a and IgG2c in the sera and IgA responses in the feces and intestines. Notably, upon challenge infection with C. sinensis metacercariae, significantly lower adult worm loads (70.2%) were measured in the liver of rats immunized with VLPs, compared to those of naïve rats. Furthermore, VLPs immunization induced antibody secreting cells (ASC) responses and CD4+/CD8+ T cell responses in the spleen.

Conclusions: Our results indicated that VLPs vaccine containing C. sinensis CsTP 22.3 kDa provided partial protection against C. sisnensis infection. Thus, VLPs could be a potential vaccine candidate against C. sinensis.

Keywords: Clonorchis sinensis; Protection; Vaccine; Virus-like particles.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Administration, Intranasal
  • Animals
  • Antibodies, Helminth / analysis
  • Antibodies, Helminth / blood*
  • Antigens, Helminth / genetics
  • Antigens, Helminth / immunology*
  • Clonorchiasis / immunology
  • Clonorchiasis / prevention & control*
  • Clonorchis sinensis / immunology*
  • Disease Models, Animal
  • Drug Carriers*
  • Feces / chemistry
  • Immunoglobulin A / analysis
  • Immunoglobulin G / blood
  • Liver / pathology
  • Parasite Load
  • Rats, Sprague-Dawley
  • Vaccines, Synthetic / administration & dosage
  • Vaccines, Synthetic / genetics
  • Vaccines, Synthetic / immunology
  • Vaccines, Virus-Like Particle / administration & dosage
  • Vaccines, Virus-Like Particle / genetics
  • Vaccines, Virus-Like Particle / immunology*
  • Viral Matrix Proteins / genetics*

Substances

  • Antibodies, Helminth
  • Antigens, Helminth
  • Drug Carriers
  • Immunoglobulin A
  • Immunoglobulin G
  • M1 protein, Influenza A virus
  • Vaccines, Synthetic
  • Vaccines, Virus-Like Particle
  • Viral Matrix Proteins