Development of T cell antigen-based human coronavirus vaccines against nAb-escaping SARS-CoV-2 variants

  • Hao Zhou*
  • , Ping Leng
  • , Yang Wang
  • , Kaiwen Yang
  • , Chen Li
  • , David M. Ojcius
  • , Pengfei Wang
  • , Shibo Jiang
  • *Corresponding author for this work

Research output: Contribution to journalReview articlepeer-review

7 Scopus citations

Abstract

Currently approved vaccines have been successful in preventing the severity of COVID-19 and hospitalization. These vaccines primarily induce humoral immune responses; however, highly transmissible and mutated variants, such as the Omicron variant, weaken the neutralization potential of the vaccines, thus, raising serious concerns about their efficacy. Additionally, while neutralizing antibodies (nAbs) tend to wane more rapidly than cell-mediated immunity, long-lasting T cells typically prevent severe viral illness by directly killing infected cells or aiding other immune cells. Importantly, T cells are more cross-reactive than antibodies, thus, highly mutated variants are less likely to escape lasting broadly cross-reactive T cell immunity. Therefore, T cell antigen-based human coronavirus (HCoV) vaccines with the potential to serve as a supplementary weapon to combat emerging SARS-CoV-2 variants with resistance to nAbs are urgently needed. Alternatively, T cell antigens could also be included in B cell antigen-based vaccines to strengthen vaccine efficacy. This review summarizes recent advancements in research and development of vaccines containing T cell antigens or both T and B cell antigens derived from proteins of SARS-CoV-2 variants and/or other HCoVs based on different vaccine platforms.

Original languageEnglish
Pages (from-to)2456-2470
Number of pages15
JournalScience Bulletin
Volume69
Issue number15
DOIs
StatePublished - 15 08 2024
Externally publishedYes

Bibliographical note

Publisher Copyright:
© 2024 Science China Press

Keywords

  • COVID-19
  • Immune escape
  • Omicron variant
  • SARS-CoV-2
  • T cell antigen-based vaccine

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