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

INTRODUCTION: Tick-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...

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Detalles Bibliográficos
Autores principales: Kubinski, Mareike, Beicht, Jana, Zdora, Isabel, Biermann, Jeannine, Puff, Christina, Gerlach, Thomas, Tscherne, Alina, Baumgärtner, Wolfgang, Osterhaus, Albert D. M. E., Sutter, Gerd, Prajeeth, Chittappen Kandiyil, Rimmelzwaan, Guus F.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10160477/
https://www.ncbi.nlm.nih.gov/pubmed/37153588
http://dx.doi.org/10.3389/fimmu.2023.1182963
Descripción
Sumario:INTRODUCTION: Tick-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. METHODS: In 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). RESULTS: MVA-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. DISCUSSION: Our data indicate that MVA-prME holds promise as an improved next-generation vaccine for the prevention of TBE.