Frontiers in Immunology (Apr 2023)

A recombinant Modified Vaccinia virus Ankara expressing prME of tick-borne encephalitis virus affords mice full protection against TBEV infection

  • Mareike Kubinski,
  • Jana Beicht,
  • Isabel Zdora,
  • Isabel Zdora,
  • Jeannine Biermann,
  • Christina Puff,
  • Thomas Gerlach,
  • Alina Tscherne,
  • Alina Tscherne,
  • Wolfgang Baumgärtner,
  • Wolfgang Baumgärtner,
  • Albert D. M. E. Osterhaus,
  • Gerd Sutter,
  • Gerd Sutter,
  • Chittappen Kandiyil Prajeeth,
  • Guus F. Rimmelzwaan

DOI
https://doi.org/10.3389/fimmu.2023.1182963
Journal volume & issue
Vol. 14

Abstract

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IntroductionTick-borne encephalitis virus (TBEV) is an important human pathogen that can cause a serious disease involving the central nervous system (tick-borne encephalitis, TBE). Although approved inactivated vaccines are available, the number of TBE cases is rising, and breakthrough infections in fully vaccinated subjects have been reported in recent years.MethodsIn the present study, we generated and characterized a recombinant Modified Vaccinia virus Ankara (MVA) for the delivery of the pre-membrane (prM) and envelope (E) proteins of TBEV (MVA-prME).ResultsMVA-prME was tested in mice in comparison with a licensed vaccine FSME-IMMUN® and proved to be highly immunogenic and afforded full protection against challenge infection with TBEV.DiscussionOur data indicate that MVA-prME holds promise as an improved next-generation vaccine for the prevention of TBE.

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