C5a receptor targeting of partial non-structural protein 3 of dengue virus promotes antigen-specific IFN-γ-producing T-cell responses in a mucosal dengue vaccine model

Cell Immunol. 2018 Mar:325:41-47. doi: 10.1016/j.cellimm.2018.01.016. Epub 2018 Feb 15.

Abstract

Mucosal vaccination is an ideal strategy to induce protective immunity in both mucosal and parenteral areas. Successful induction of an antigen-specific immune response via mucosal administration essentially requires the effective delivery of antigen into a mucosal immune inductive site, which depends on antigen delivery into M cells. We previously reported that M cells specifically express C5aR, and antigen targeting to C5aR by using specific ligands, including Co1 peptide, promotes the antigen-specific immune response in both mucosal and systemic immune compartments. In this study, we found that application of the Co1 peptide to dengue virus antigen containing CD8 T cell epitopes effectively induced an antigen-specific IFN-γ-producing CD8+ T cell response after oral mucosal administration of antigen. Consequently, we suggest that Co1 peptide-mediated C5aR targeting of antigen into M cells can be used for the induction of an effective antigen-specific CD8+ T cell immune response in oral mucosal vaccine development.

Keywords: C5a receptor; CD8(+) T lymphocyte; Dengue virus; Mucosal immunity.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antigens
  • Antigens, Viral / immunology
  • CD8-Positive T-Lymphocytes / immunology
  • Dengue Vaccines / metabolism*
  • Dengue Virus / metabolism
  • Disease Models, Animal
  • Immunity, Mucosal / immunology
  • Mice
  • Mice, Inbred BALB C
  • Mucous Membrane / immunology
  • Receptor, Anaphylatoxin C5a / metabolism*
  • Vaccination
  • Viral Nonstructural Proteins / immunology*
  • Viral Nonstructural Proteins / metabolism

Substances

  • Antigens
  • Antigens, Viral
  • Dengue Vaccines
  • Receptor, Anaphylatoxin C5a
  • Viral Nonstructural Proteins