Frontiers in Cellular and Infection Microbiology (Aug 2023)

Vaccination with the Crimean-Congo hemorrhagic fever virus viral replicon vaccine induces NP-based T-cell activation and antibodies possessing Fc-mediated effector functions

  • F. E. M. Scholte,
  • E. Karaaslan,
  • E. Karaaslan,
  • T. J. O’Neal,
  • T. E. Sorvillo,
  • S. C. Genzer,
  • S. R. Welch,
  • J. D. Coleman-McCray,
  • J. R. Spengler,
  • M. H. Kainulainen,
  • J. M. Montgomery,
  • S. D. Pegan,
  • E. Bergeron,
  • C. F. Spiropoulou

DOI
https://doi.org/10.3389/fcimb.2023.1233148
Journal volume & issue
Vol. 13

Abstract

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Crimean-Congo hemorrhagic fever virus (CCHFV; family Nairoviridae) is a tick-borne pathogen that frequently causes lethal disease in humans. CCHFV has a wide geographic distribution, and cases have been reported in Africa, Asia, the Middle East, and Europe. Availability of a safe and efficacious vaccine is critical for restricting outbreaks and preventing disease in endemic countries. We previously developed a virus-like replicon particle (VRP) vaccine that provides complete protection against homologous and heterologous lethal CCHFV challenge in mice after a single dose. However, the immune responses induced by this vaccine are not well characterized, and correlates of protection remain unknown. Here we comprehensively characterized the kinetics of cell-mediated and humoral immune responses in VRP-vaccinated mice, and demonstrate that they predominantly target the nucleoprotein (NP). NP antibodies are not associated with protection through neutralizing activity, but VRP vaccination results in NP antibodies possessing Fc-mediated antibody effector functions, such as complement activation (ADCD) and antibody-mediated cellular phagocytosis (ADCP). This suggests that Fc-mediated effector functions may contribute to this vaccine’s efficacy.

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