Evidence map›Paper›PMID 28819261›Full record

ArticleScientific reports2017

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

Arwen F Altenburg, Carolien E van de Sandt, Bobby W S Li, Ronan J MacLoughlin, Ron A M Fouchier, Geert van Amerongen, Asisa Volz, Rudi W Hendriks, Rik L de Swart, Gerd Sutter and 2 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
2.1field-weighted citation impact, top 14% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

26 citing papers in PubMed, 38 citations in OpenAlex.

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  11. Viral vector-based gene therapies in the clinic.Bioengineering & translational medicine · 2022
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  15. Cellular Therapy for the Treatment of Paediatric Respiratory Disease.International journal of molecular sciences · 2021
    Review
  16. Article
  17. Review
  18. Precise Targeting of miRNA Sites Restores CFTR Activity in CF Bronchial Epithelial Cells.Molecular therapy : the journal of the American Society of Gene Therapy · 2020
    Article
  19. Article
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

12 authors at 4 institutions in 3 countries.

Arwen F AltenburgDepartment of Viroscience, Postgraduate School of Molecular Medicine, Erasmus MC, Rotterdam, The Netherlands.
Carolien E van de SandtDepartment of Viroscience, Postgraduate School of Molecular Medicine, Erasmus MC, Rotterdam, The Netherlands.
Bobby W S LiDepartment of Pulmonary Medicine, Erasmus MC, Rotterdam, The Netherlands.
Ronan J MacLoughlinAerogen Ltd, IDA Business Park, Dangan, Galway, Ireland.
Ron A M FouchierDepartment of Viroscience, Postgraduate School of Molecular Medicine, Erasmus MC, Rotterdam, The Netherlands.
Geert van AmerongenViroClinics Biosciences BV, Rotterdam, The Netherlands.
Asisa VolzInstitute for Infectious Diseases and Zoonoses, LMU University of Munich, Munich, Germany.
Rudi W HendriksDepartment of Pulmonary Medicine, Erasmus MC, Rotterdam, The Netherlands.
Rik L de SwartDepartment of Viroscience, Postgraduate School of Molecular Medicine, Erasmus MC, Rotterdam, The Netherlands.
Gerd SutterInstitute for Infectious Diseases and Zoonoses, LMU University of Munich, Munich, Germany.
Guus F RimmelzwaanDepartment of Viroscience, Postgraduate School of Molecular Medicine, Erasmus MC, Rotterdam, The Netherlands.
Rory D de VriesDepartment of Viroscience, Postgraduate School of Molecular Medicine, Erasmus MC, Rotterdam, The Netherlands. r.d.devries@erasmusmc.nl.
Erasmus MC · NLGerman Center for Infection Research · DEAerogen (Ireland) · IEViroclinics Biosciences (Netherlands) · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

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.

Indexed as

AnimalsAntigen-Presenting CellsDendritic CellsFerretsGreen Fluorescent ProteinsHumansLeukocytes, MononuclearMacaca fascicularisMacrophages, AlveolarMiceMicroscopy, ConfocalMuscle CellsRecombinant Fusion ProteinsVaccinia virusViral VaccinesGreen Fluorescent ProteinsRecombinant Fusion ProteinsViral Vaccines

Identifiers

PMID28819261
PMCPMC5561217
OpenAlexW2743783127

What OpenQuestion holds

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LicenceCC BY
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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.