Coated protein nanoclusters from influenza H7N9 HA are highly immunogenic and induce robust protective immunity

Nanomedicine. 2017 Jan;13(1):253-262. doi: 10.1016/j.nano.2016.09.001. Epub 2016 Sep 10.

Abstract

Recurring influenza viruses pose an annual threat to public health. A time-saving, cost-effective and egg-independent influenza vaccine approach is important particularly when responding to an emerging pandemic. We fabricated coated, two-layer protein nanoclusters from recombinant trimeric hemagglutinin from an avian-origin H7N9 influenza A virus as an approach for vaccine development in response to an emerging pandemic. Assessment of the virus-specific immune responses and protective efficacy in mice immunized with the nanoclusters demonstrated that the vaccine candidates were highly immunogenic, able to induce protective immunity and long-lasting humoral antibody responses to this virus without the use of adjuvants. Because the advantages of the highly immunogenic coated nanoclusters also include rapid productions in an egg-independent system, this approach has great potential for influenza vaccine production not only in response to an emerging pandemic, but also as a replacement for conventional seasonal influenza vaccines.

Keywords: Influenza vaccine; Pandemic influenza; Protein nanoclusters.

MeSH terms

  • Animals
  • Antibodies, Viral / blood
  • Enzyme-Linked Immunosorbent Assay
  • Female
  • Hemagglutinin Glycoproteins, Influenza Virus / immunology*
  • Immunity, Humoral
  • Influenza A Virus, H7N9 Subtype
  • Influenza Vaccines / immunology*
  • Mice
  • Mice, Inbred BALB C
  • Nanoparticles / chemistry*
  • Neutralization Tests
  • Orthomyxoviridae Infections / prevention & control*
  • Recombinant Proteins / immunology

Substances

  • Antibodies, Viral
  • Hemagglutinin Glycoproteins, Influenza Virus
  • Influenza Vaccines
  • Recombinant Proteins
  • hemagglutinin, human influenza A virus