Frontiers in Immunology (Dec 2021)

A Highly Conserved Peptide Vaccine Candidate Activates Both Humoral and Cellular Immunity Against SARS-CoV-2 Variant Strains

  • Fengxia Gao,
  • Fengxia Gao,
  • Jingjing Huang,
  • Jingjing Huang,
  • Tingting Li,
  • Tingting Li,
  • Chao Hu,
  • Chao Hu,
  • Meiying Shen,
  • Song Mu,
  • Song Mu,
  • Feiyang Luo,
  • Feiyang Luo,
  • Shuyi Song,
  • Shuyi Song,
  • Yanan Hao,
  • Yanan Hao,
  • Wang Wang,
  • Wang Wang,
  • Xiaojian Han,
  • Xiaojian Han,
  • Chen Qian,
  • Chen Qian,
  • Yingming Wang,
  • Yingming Wang,
  • Ruixin Wu,
  • Ruixin Wu,
  • Luo Li,
  • Luo Li,
  • Shenglong Li,
  • Shenglong Li,
  • Aishun Jin,
  • Aishun Jin

DOI
https://doi.org/10.3389/fimmu.2021.789905
Journal volume & issue
Vol. 12

Abstract

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Facing the imminent need for vaccine candidates with cross-protection against globally circulating severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) mutants, we present a conserved antigenic peptide RBD9.1 with both T-cell and B-cell epitopes. RBD9.1 can be recognized by coronavirus disease 2019 (COVID-19) convalescent serum, particularly for those with high neutralizing potency. Immunization with RBD9.1 can successfully induce the production of the receptor-binding domain (RBD)-specific antibodies in Balb/c mice. Importantly, the immunized sera exhibit sustained neutralizing efficacy against multiple dominant SARS-CoV-2 variant strains, including B.1.617.2 that carries a point mutation (SL452R) within the sequence of RBD9.1. Specifically, SY451 and SY454 are identified as the key amino acids for the binding of the induced RBD-specific antibodies to RBD9.1. Furthermore, we have confirmed that the RBD9.1 antigenic peptide can induce a S448-456 (NYNYLYRLF)-specific CD8+ T-cell response. Both RBD9.1-specific B cells and the S448-456-specific T cells can still be activated more than 3 months post the last immunization. This study provides a potential vaccine candidate that can generate long-term protective efficacy over SARS-CoV-2 variants, with the unique functional mechanism of activating both humoral and cellular immunity.

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