Emerging Microbes and Infections (Jan 2021)

A novel linker-immunodominant site (LIS) vaccine targeting the SARS-CoV-2 spike protein protects against severe COVID-19 in Syrian hamsters

  • Bao-Zhong Zhang,
  • Xiaolei Wang,
  • Shuofeng Yuan,
  • Wenjun Li,
  • Ying Dou,
  • Vincent Kwok-Man Poon,
  • Chris Chung-Sing Chan,
  • Jian-Piao Cai,
  • Kenn KaHeng Chik,
  • Kaiming Tang,
  • Chris Chun-Yiu Chan,
  • Ye-Fan Hu,
  • Jing-Chu Hu,
  • Smaranda Ruxandra Badea,
  • Hua-Rui Gong,
  • Xuansheng Lin,
  • Hin Chu,
  • Xuechen Li,
  • Kelvin Kai-Wang To,
  • Li Liu,
  • Zhiwei Chen,
  • Ivan Fan-Ngai Hung,
  • Kwok Yung Yuen,
  • Jasper Fuk-Woo Chan,
  • Jian-Dong Huang

DOI
https://doi.org/10.1080/22221751.2021.1921621
Journal volume & issue
Vol. 10, no. 1
pp. 874 – 884

Abstract

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The Coronavirus Disease 2019 (COVID-19) pandemic is unlikely to abate until sufficient herd immunity is built up by either natural infection or vaccination. We previously identified ten linear immunodominant sites on the SARS-CoV-2 spike protein of which four are located within the RBD. Therefore, we designed two linkerimmunodominant site (LIS) vaccine candidates which are composed of four immunodominant sites within the RBD (RBD-ID) or all the 10 immunodominant sites within the whole spike (S-ID). They were administered by subcutaneous injection and were tested for immunogenicity and in vivo protective efficacy in a hamster model for COVID-19. We showed that the S-ID vaccine induced significantly better neutralizing antibody response than RBD-ID and alum control. As expected, hamsters vaccinated by S-ID had significantly less body weight loss, lung viral load, and histopathological changes of pneumonia. The S-ID has the potential to be an effective vaccine for protection against COVID-19.

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