Evidence map›Paper›PMID 35544042›Full record

ArticleThe Lancet. Microbe2022

Transcriptomic signatures induced by the Ebola virus vaccine rVSVΔG-ZEBOV-GP in adult cohorts in Europe, Africa, and North America: a molecular biomarker study.

Eleonora Vianello, Patricia Gonzalez-Dias, Suzanne van Veen, Carmen G Engele, Edwin Quinten, Thomas P Monath, Donata Medaglini, VSV-EBOVAC Consortium, VSV-EBOPLUS Consortium, Francesco Santoro and 11 more

Open access · goldAbstract read
In one paragraph

Article in The Lancet. Microbe, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
0.5field-weighted citation impact, top 33% 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

10 citing papers in PubMed, 12 citations in OpenAlex.

  1. Trial
  2. Microbiology spectrum · 2026
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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

21 authors at 9 institutions in 8 countries.

Eleonora VianelloDepartment of Infectious Diseases, Leiden University Medical Center, Leiden, Netherlands. Electronic address: e.vianello@lumc.nl.
Patricia Gonzalez-DiasDepartment of Clinical and Toxicological Analyses, School of Pharmaceutical Sciences, University of São Paulo, São Paulo, Brazil.
Suzanne van VeenDepartment of Infectious Diseases, Leiden University Medical Center, Leiden, Netherlands.
Carmen G EngeleDepartment of Infectious Diseases, Leiden University Medical Center, Leiden, Netherlands.
Edwin QuintenDepartment of Infectious Diseases, Leiden University Medical Center, Leiden, Netherlands.
Thomas P MonathNewLink Genetics Corporation, Devens, MA, USA.
Donata MedagliniLaboratory of Molecular Microbiology and Biotechnology, Department of Medical Biotechnologies, University of Siena, Siena, Italy; Sclavo Vaccines Association, Siena, Italy.
VSV-EBOVAC Consortium
VSV-EBOPLUS Consortium
Francesco SantoroLaboratory of Molecular Microbiology and Biotechnology, Department of Medical Biotechnologies, University of Siena, Siena, Italy.
Angela HuttnerDivision of Infectious Diseases, Geneva University Hospitals and Faculty of Medicine, Geneva, Switzerland; Center for Vaccinology, Geneva University Hospitals and Faculty of Medicine, Geneva, Switzerland.
Sheri DubeyDepartment of Vaccine and Biologics Research, Merck Research Laboratories, West Point, PA, USA.
Michael EichbergDepartment of Vaccine and Biologics Research, Merck Research Laboratories, West Point, PA, USA.
Francis M NdunguDepartment of Biosciences, KEMRI-Wellcome Trust Research Programme, Kilifi, Kenya.
Peter G KremsnerCentre de Recherches Médicales de Lambaréné, Lambaréné, Gabon; Institut für Tropenmedizin, Universitätsklinikum Tübingen, and German Center for Infection Research, Tübingen, Germany.
Paulin N EssoneCentre de Recherches Médicales de Lambaréné, Lambaréné, Gabon.
Selidji Todagbe AgnandjiCentre de Recherches Médicales de Lambaréné, Lambaréné, Gabon; Institut für Tropenmedizin, Universitätsklinikum Tübingen, and German Center for Infection Research, Tübingen, Germany.
Claire-Anne SiegristDivision of Infectious Diseases, Geneva University Hospitals and Faculty of Medicine, Geneva, Switzerland; Center for Vaccinology, Geneva University Hospitals and Faculty of Medicine, Geneva, Switzerland.
Helder I NakayaDepartment of Clinical and Toxicological Analyses, School of Pharmaceutical Sciences, University of São Paulo, São Paulo, Brazil; Scientific Platform Pasteur-USP, São Paulo, Brazil.
Tom H M OttenhoffDepartment of Infectious Diseases, Leiden University Medical Center, Leiden, Netherlands.
Mariëlle C HaksDepartment of Infectious Diseases, Leiden University Medical Center, Leiden, Netherlands.
Leiden University Medical Center · NLUniversity of Siena · ITUniversity Hospital of Geneva · CHUnited States Military Academy · USUniversidade de São Paulo · BRCentre de Recherche Médicales de Lambaréné · GAKenya Medical Research Institute · KEUniversitätsklinikum Tübingen · DENewLink Genetics (United States) · US

Funding

Wellcome Trust 203077
6 · The paper itself

Abstract

backgroundA recombinant vesicular stomatitis virus vector expressing the Zaire Ebola virus glycoprotein (rVSVΔG-ZEBOV-GP) vaccine has been reported as safe, immunogenic, and highly protective in a ring vaccination trial. We aimed to identify transcriptomic immune response biomarker signatures induced by vaccination and associated signatures with its immunogenicity and reactogenicity to better understand the potential mechanisms of action of the vaccine.

methods354 healthy adult volunteers were vaccinated in randomised, double-blind, placebo-controlled trials in Europe (Geneva, Switzerland [November, 2014, to January, 2015]) and North America (USA [Dec 5, 2014, to June 23, 2015]), and dose-escalation trials in Africa (Lambaréné, Gabon [November, 2014, to January, 2015], and Kilifi, Kenya [December, 2014, to January, 2015]) using different doses of the recombinant vesicular stomatitis virus vector expressing the Zaire Ebola virus glycoprotein (rVSVΔG-ZEBOV-GP; 3 × 10

findingsOur results indicated that perturbation of gene expression peaked on day 1 and returned to baseline levels between day 7 and day 28. The magnitude of the response was dose-dependent, with vaccinees receiving a high dose (≥9 × 10

interpretationCollectively, our results identify and cross-validate immune-related transcriptomic signatures induced by rVSVΔG-ZEBOV-GP vaccination in four cohorts of adult participants from different genetic and geographical backgrounds. These signatures will aid in the rational development, testing, and evaluation of novel vaccines and will allow evaluation of the effect of host factors such as age, co-infection, and comorbidity on responses to vaccines.

fundingInnovative Medicines Initiative 2 Joint Undertaking.

Indexed as

Ebola VaccinesEbolavirusHemorrhagic Fever, EbolaVesicular StomatitisAdultAfricaAntibodies, ViralBiomarkersEuropeGlycoproteinsHumansNorth AmericaRandomized Controlled Trials as TopicTranscriptomeVesiculovirusAntibodies, ViralBiomarkersEbola VaccinesGlycoproteins

Identifiers

PMID35544042
PMCPMC7613316
OpenAlexW4200560137

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.