Early insight into antibody-dependent enhancement after SARS-CoV-2 mRNA vaccination

Hum Vaccin Immunother. 2021 Nov 2;17(11):4121-4125. doi: 10.1080/21645515.2021.1969855. Epub 2021 Sep 20.

Abstract

Current vaccines, which induce a B-cell-mediated antibody response against the spike protein of SARS-CoV-2, have markedly reduced infection rates. However, the emergence of new variants as a result of SARS-CoV-2 evolution requires the development of novel vaccines that are T-cell-based and that target mutant-specific spike proteins along with ORF1ab or nucleocapsid protein. This approach is more accommodative in inducing highly neutralizing antibodies, without the risk of antibody-dependent enhancement, as well as memory CD8+T-cell immunity.

Keywords: COVID-19; SARS-CoV-2; antibodies; antibody-dependent enhancement; neutralization; spike protein; vaccine.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antibodies, Neutralizing
  • Antibodies, Viral
  • Antibody-Dependent Enhancement*
  • COVID-19*
  • Humans
  • RNA, Messenger
  • SARS-CoV-2
  • Spike Glycoprotein, Coronavirus
  • Vaccination

Substances

  • Antibodies, Neutralizing
  • Antibodies, Viral
  • RNA, Messenger
  • Spike Glycoprotein, Coronavirus

Grants and funding

This work was supported by the Kuwait Foundation for the Advancement of Sciences (KFAS) under Grant CORONA PROP 10.