Kinetically activating nanovaccine mimicking multidimensional immunomodulation of natural infection for broad protection against heterologous viruses in animal models

  • Sang Nam Lee
  • , Young Il Kim
  • , Jaemoo Kim
  • , D. K. Haluwana
  • , Ryounho Eun
  • , Sei Hyun Park
  • , Janghun Heo
  • , Juryeon Gil
  • , Yebin Seong
  • , Min Ho Lee
  • , Young Woock Noh
  • , Jong Soo Lee
  • , Young Ki Choi
  • , Yong Taik Lim

Research output: Contribution to journalArticlepeer-review

2 Scopus citations

Abstract

Immunity by vaccination can protect human against heterologous viruses. However, protective abilities of artificial vaccines are still weaker than natural infections. Here we develop a kinetically engineered vaccine (KE-VAC) that mimics the multidimensional immunomodulation in natural infections via dynamic activation of antigen presenting cells with masked TLR7/8 agonist and sustained supplies of antigens and adjuvants to lymph nodes, leading to follicular helper T and germinal centre B cell activation in vaccinated mice. KE-VAC demonstrates superior efficacy than traditional alum and mRNA vaccines, achieving a 100% survival rate with increased neutralizing antibodies titers and polyfunctional CD8+ T cells, recognizing heterologous SARS-CoV-2 variants, and inducing broad and long-term protection against multiple strains of influenza viruses. Prime/boost vaccination with KE-VAC also protect aged ferrets from severe fever with thrombocytopenia syndrome virus infection, with no virus detected in any organs at day 6 p.i. The efficacy of KE-VAC across various pathogens thus highlights its potential as an effective vaccine against emerging infectious risks.

Original languageEnglish
Article number2914
JournalNature Communications
Volume16
Issue number1
DOIs
StatePublished - Dec 2025
Externally publishedYes

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

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