Identification of a Spike-Specific CD8+ T-Cell Epitope Following Vaccination Against the Middle East Respiratory Syndrome Coronavirus in Humans

J Infect Dis. 2024 Aug 16;230(2):e327-e332. doi: 10.1093/infdis/jiad612.

Abstract

Licensed vaccines against the Middle East respiratory syndrome coronavirus (MERS-CoV), an emerging pathogen of concern, are lacking. The modified vaccinia virus Ankara vector-based vaccine MVA-MERS-S, expressing the MERS-CoV-spike glycoprotein (MERS-S), is one of 3 candidate vaccines in clinical development and elicits robust humoral and cellular immunity. Here, we identified for the first time a MERS-S-specific CD8+ T-cell epitope in an HLA-A*03:01/HLA-B*35:01-positive vaccinee using a screening assay, intracellular cytokine staining, and in silico epitope prediction. As evidence from MERS-CoV infection suggests a protective role of long-lasting CD8+ T-cell responses, the identification of epitopes will facilitate longitudinal analyses of vaccine-induced T-cell immunity.

Keywords: CD8+ T cells; MERS-CoV; MVA; epitope; vaccine; viral vector.

MeSH terms

  • CD8-Positive T-Lymphocytes* / immunology
  • Coronavirus Infections / immunology
  • Coronavirus Infections / prevention & control
  • Epitopes, T-Lymphocyte* / immunology
  • Humans
  • Middle East Respiratory Syndrome Coronavirus* / immunology
  • Spike Glycoprotein, Coronavirus* / immunology
  • Vaccination
  • Viral Vaccines* / immunology

Substances

  • Epitopes, T-Lymphocyte
  • Spike Glycoprotein, Coronavirus
  • Viral Vaccines