Signal Transduction and Targeted Therapy (May 2021)

A core-shell structured COVID-19 mRNA vaccine with favorable biodistribution pattern and promising immunity

  • Ren Yang,
  • Yao Deng,
  • Baoying Huang,
  • Lei Huang,
  • Ang Lin,
  • Yuhua Li,
  • Wenling Wang,
  • Jingjing Liu,
  • Shuaiyao Lu,
  • Zhenzhen Zhan,
  • Yufei Wang,
  • Ruhan A,
  • Wen Wang,
  • Peihua Niu,
  • Li Zhao,
  • Shiqiang Li,
  • Xiaopin Ma,
  • Luyao Zhang,
  • Yujian Zhang,
  • Weiguo Yao,
  • Xingjie Liang,
  • Jincun Zhao,
  • Zhongmin Liu,
  • Xiaozhong Peng,
  • Hangwen Li,
  • Wenjie Tan

DOI
https://doi.org/10.1038/s41392-021-00634-z
Journal volume & issue
Vol. 6, no. 1
pp. 1 – 10

Abstract

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Abstract Although inoculation of COVID-19 vaccines has rolled out globally, there is still a critical need for safe and effective vaccines to ensure fair and equitable supply for all countries. Here, we report on the development of a highly efficacious mRNA vaccine, SW0123 that is composed of sequence-modified mRNA encoding the full-length SARS-CoV-2 Spike protein packaged in core–shell structured lipopolyplex (LPP) nanoparticles. SW0123 is easy to produce using a large-scale microfluidics-based apparatus. The unique core–shell structured nanoparticle facilitates vaccine uptake and demonstrates a high colloidal stability, and a desirable biodistribution pattern with low liver targeting effect upon intramuscular administration. Extensive evaluations in mice and nonhuman primates revealed strong immunogenicity of SW0123, represented by induction of Th1-polarized T cell responses and high levels of antibodies that were capable of neutralizing not only the wild-type SARS-CoV-2, but also a panel of variants including D614G and N501Y variants. In addition, SW0123 conferred effective protection in both mice and non-human primates upon SARS-CoV-2 challenge. Taken together, SW0123 is a promising vaccine candidate that holds prospects for further evaluation in humans.