Co-administration of non-carrier nanoparticles boosts antigen immune response without requiring protein conjugation

Vaccine. 2014 Jun 17;32(29):3664-9. doi: 10.1016/j.vaccine.2014.04.043. Epub 2014 Apr 29.

Abstract

Nanotechnology promises a revolution in medicine including through new vaccine approaches. The use of nanoparticles in vaccination has, to date, focused on attaching antigen directly to or within nanoparticle structures to enhance antigen uptake by immune cells. Here we question whether antigen incorporation with the nanoparticle is actually necessary to boost vaccine effectiveness. We show that the immunogenicity of a sub-unit protein antigen was significantly boosted by formulation with silica nanoparticles even without specific conjugation of antigen to the nanoparticle. We further show that this effect was observed only for virus-sized nanoparticles (50 nm) but not for larger (1,000 nm) particles, demonstrating a pronounced effect of nanoparticle size. This non-attachment approach has potential to radically simplify the development and application of nanoparticle-based formulations, leading to safer and simpler nanoparticle applications in vaccine development.

Keywords: Adjuvant; Capsomere; Nanoparticle; Silica; Vaccine; Virus-like particle.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adjuvants, Immunologic / administration & dosage*
  • Aluminum Hydroxide / administration & dosage
  • Animals
  • Antibodies, Viral / blood
  • Antigens / immunology*
  • Escherichia coli / metabolism
  • Genetic Vectors
  • Immunoglobulin G / blood
  • Influenza Vaccines / immunology*
  • Mice, Inbred BALB C
  • Nanoparticles / administration & dosage*
  • Particle Size
  • Silicon Dioxide / administration & dosage
  • Viral Matrix Proteins / immunology

Substances

  • Adjuvants, Immunologic
  • Antibodies, Viral
  • Antigens
  • Immunoglobulin G
  • Influenza Vaccines
  • M2 protein, Influenza A virus
  • Viral Matrix Proteins
  • Aluminum Hydroxide
  • Silicon Dioxide