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Modified Vaccinia Virus Ankara Preferentially Targets Antigen Presenting Cells In Vitro, Ex Vivo and In Vivo

Modified Vaccinia virus Ankara (MVA) is a promising vaccine vector with an excellent safety profile. However, despite extensive pre-clinical and clinical testing, surprisingly little is known about the cellular tropism of MVA, especially in relevant animal species. Here, we performed in vitro, ex vi...

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Autores principales: Altenburg, Arwen F., van de Sandt, Carolien E., Li, Bobby W. S., MacLoughlin, Ronan J., Fouchier, Ron A. M., van Amerongen, Geert, Volz, Asisa, Hendriks, Rudi W., de Swart, Rik L., Sutter, Gerd, Rimmelzwaan, Guus F., de Vries, Rory D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5561217/
https://www.ncbi.nlm.nih.gov/pubmed/28819261
http://dx.doi.org/10.1038/s41598-017-08719-y
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author Altenburg, Arwen F.
van de Sandt, Carolien E.
Li, Bobby W. S.
MacLoughlin, Ronan J.
Fouchier, Ron A. M.
van Amerongen, Geert
Volz, Asisa
Hendriks, Rudi W.
de Swart, Rik L.
Sutter, Gerd
Rimmelzwaan, Guus F.
de Vries, Rory D.
author_facet Altenburg, Arwen F.
van de Sandt, Carolien E.
Li, Bobby W. S.
MacLoughlin, Ronan J.
Fouchier, Ron A. M.
van Amerongen, Geert
Volz, Asisa
Hendriks, Rudi W.
de Swart, Rik L.
Sutter, Gerd
Rimmelzwaan, Guus F.
de Vries, Rory D.
author_sort Altenburg, Arwen F.
collection PubMed
description Modified Vaccinia virus Ankara (MVA) is a promising vaccine vector with an excellent safety profile. However, despite extensive pre-clinical and clinical testing, surprisingly little is known about the cellular tropism of MVA, especially in relevant animal species. Here, we performed in vitro, ex vivo and in vivo experiments with recombinant MVA expressing green fluorescent protein (rMVA-GFP). In both human peripheral blood mononuclear cells and mouse lung explants, rMVA-GFP predominantly infected antigen presenting cells. Subsequent in vivo experiments performed in mice, ferrets and non-human primates indicated that preferential targeting of dendritic cells and alveolar macrophages was observed after respiratory administration, although subtle differences were observed between the respective animal species. Following intramuscular injection, rMVA-GFP was detected in interdigitating cells between myocytes, but also in myocytes themselves. These data are important in advancing our understanding of the basis for the immunogenicity of MVA-based vaccines and aid rational vaccine design and delivery strategies.
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spelling pubmed-55612172017-08-21 Modified Vaccinia Virus Ankara Preferentially Targets Antigen Presenting Cells In Vitro, Ex Vivo and In Vivo Altenburg, Arwen F. van de Sandt, Carolien E. Li, Bobby W. S. MacLoughlin, Ronan J. Fouchier, Ron A. M. van Amerongen, Geert Volz, Asisa Hendriks, Rudi W. de Swart, Rik L. Sutter, Gerd Rimmelzwaan, Guus F. de Vries, Rory D. Sci Rep Article Modified Vaccinia virus Ankara (MVA) is a promising vaccine vector with an excellent safety profile. However, despite extensive pre-clinical and clinical testing, surprisingly little is known about the cellular tropism of MVA, especially in relevant animal species. Here, we performed in vitro, ex vivo and in vivo experiments with recombinant MVA expressing green fluorescent protein (rMVA-GFP). In both human peripheral blood mononuclear cells and mouse lung explants, rMVA-GFP predominantly infected antigen presenting cells. Subsequent in vivo experiments performed in mice, ferrets and non-human primates indicated that preferential targeting of dendritic cells and alveolar macrophages was observed after respiratory administration, although subtle differences were observed between the respective animal species. Following intramuscular injection, rMVA-GFP was detected in interdigitating cells between myocytes, but also in myocytes themselves. These data are important in advancing our understanding of the basis for the immunogenicity of MVA-based vaccines and aid rational vaccine design and delivery strategies. Nature Publishing Group UK 2017-08-17 /pmc/articles/PMC5561217/ /pubmed/28819261 http://dx.doi.org/10.1038/s41598-017-08719-y Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Altenburg, Arwen F.
van de Sandt, Carolien E.
Li, Bobby W. S.
MacLoughlin, Ronan J.
Fouchier, Ron A. M.
van Amerongen, Geert
Volz, Asisa
Hendriks, Rudi W.
de Swart, Rik L.
Sutter, Gerd
Rimmelzwaan, Guus F.
de Vries, Rory D.
Modified Vaccinia Virus Ankara Preferentially Targets Antigen Presenting Cells In Vitro, Ex Vivo and In Vivo
title Modified Vaccinia Virus Ankara Preferentially Targets Antigen Presenting Cells In Vitro, Ex Vivo and In Vivo
title_full Modified Vaccinia Virus Ankara Preferentially Targets Antigen Presenting Cells In Vitro, Ex Vivo and In Vivo
title_fullStr Modified Vaccinia Virus Ankara Preferentially Targets Antigen Presenting Cells In Vitro, Ex Vivo and In Vivo
title_full_unstemmed Modified Vaccinia Virus Ankara Preferentially Targets Antigen Presenting Cells In Vitro, Ex Vivo and In Vivo
title_short Modified Vaccinia Virus Ankara Preferentially Targets Antigen Presenting Cells In Vitro, Ex Vivo and In Vivo
title_sort modified vaccinia virus ankara preferentially targets antigen presenting cells in vitro, ex vivo and in vivo
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5561217/
https://www.ncbi.nlm.nih.gov/pubmed/28819261
http://dx.doi.org/10.1038/s41598-017-08719-y
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