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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...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2023
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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 |
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author | 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. |
author_facet | 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. |
author_sort | Kubinski, Mareike |
collection | PubMed |
description | 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. |
format | Online Article Text |
id | pubmed-10160477 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-101604772023-05-06 A recombinant Modified Vaccinia virus Ankara expressing prME of tick-borne encephalitis virus affords mice full protection against TBEV infection 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. Front Immunol Immunology 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. Frontiers Media S.A. 2023-04-21 /pmc/articles/PMC10160477/ /pubmed/37153588 http://dx.doi.org/10.3389/fimmu.2023.1182963 Text en Copyright © 2023 Kubinski, Beicht, Zdora, Biermann, Puff, Gerlach, Tscherne, Baumgärtner, Osterhaus, Sutter, Prajeeth and Rimmelzwaan https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Immunology 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. A recombinant Modified Vaccinia virus Ankara expressing prME of tick-borne encephalitis virus affords mice full protection against TBEV infection |
title | A recombinant Modified Vaccinia virus Ankara expressing prME of tick-borne encephalitis virus affords mice full protection against TBEV infection |
title_full | A recombinant Modified Vaccinia virus Ankara expressing prME of tick-borne encephalitis virus affords mice full protection against TBEV infection |
title_fullStr | A recombinant Modified Vaccinia virus Ankara expressing prME of tick-borne encephalitis virus affords mice full protection against TBEV infection |
title_full_unstemmed | A recombinant Modified Vaccinia virus Ankara expressing prME of tick-borne encephalitis virus affords mice full protection against TBEV infection |
title_short | A recombinant Modified Vaccinia virus Ankara expressing prME of tick-borne encephalitis virus affords mice full protection against TBEV infection |
title_sort | recombinant modified vaccinia virus ankara expressing prme of tick-borne encephalitis virus affords mice full protection against tbev infection |
topic | Immunology |
url | 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 |
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