PLoS Pathogens (Sep 2021)

Novel virus-like nanoparticle vaccine effectively protects animal model from SARS-CoV-2 infection.

  • Qibin Geng,
  • Wanbo Tai,
  • Victoria K Baxter,
  • Juan Shi,
  • Yushun Wan,
  • Xiujuan Zhang,
  • Stephanie A Montgomery,
  • Sharon A Taft-Benz,
  • Elizabeth J Anderson,
  • Audrey C Knight,
  • Kenneth H Dinnon,
  • Sarah R Leist,
  • Ralph S Baric,
  • Jian Shang,
  • Sung-Wook Hong,
  • Aleksandra Drelich,
  • Chien-Te K Tseng,
  • Marc Jenkins,
  • Mark Heise,
  • Lanying Du,
  • Fang Li

DOI
https://doi.org/10.1371/journal.ppat.1009897
Journal volume & issue
Vol. 17, no. 9
p. e1009897

Abstract

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The key to battling the COVID-19 pandemic and its potential aftermath is to develop a variety of vaccines that are efficacious and safe, elicit lasting immunity, and cover a range of SARS-CoV-2 variants. Recombinant viral receptor-binding domains (RBDs) are safe vaccine candidates but often have limited efficacy due to the lack of virus-like immunogen display pattern. Here we have developed a novel virus-like nanoparticle (VLP) vaccine that displays 120 copies of SARS-CoV-2 RBD on its surface. This VLP-RBD vaccine mimics virus-based vaccines in immunogen display, which boosts its efficacy, while maintaining the safety of protein-based subunit vaccines. Compared to the RBD vaccine, the VLP-RBD vaccine induced five times more neutralizing antibodies in mice that efficiently blocked SARS-CoV-2 from attaching to its host receptor and potently neutralized the cell entry of variant SARS-CoV-2 strains, SARS-CoV-1, and SARS-CoV-1-related bat coronavirus. These neutralizing immune responses induced by the VLP-RBD vaccine did not wane during the two-month study period. Furthermore, the VLP-RBD vaccine effectively protected mice from SARS-CoV-2 challenge, dramatically reducing the development of clinical signs and pathological changes in immunized mice. The VLP-RBD vaccine provides one potentially effective solution to controlling the spread of SARS-CoV-2.