Evidence map›Paper›PMID 30407513›Full record

Trial reportThe Journal of infectious diseases2019

Safety and Immunogenicity of a Heterologous Prime-Boost Ebola Virus Vaccine Regimen in Healthy Adults in the United Kingdom and Senegal.

Navin Venkatraman, Birahim Pierre Ndiaye, Georgina Bowyer, Djibril Wade, Saranya Sridhar, Daniel Wright, Jonathan Powlson, Ibrahima Ndiaye, Siry Dièye, Craig Thompson and 20 more

2 registry-linked trialsOpen access · hybridAbstract readClinical Trial, Phase IClinical Trial, Phase IIRandomized Controlled Trial
In one paragraph

Trial report in The Journal of infectious diseases, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 2 registered trials, which are not on this map. Cited by 56 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
56citing papers in PubMed, 1 pooled it
5.6field-weighted citation impact, top 3% 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.

NCT02451891 phase1terminatednot on this map

A Phase Ia Clinical Trial to Assess the Safety and Immunogenicity of MVA-EBO Z Alone and a Heterologous Prime-boost Immunisation With ChAd3-EBO Z and MVA-EBO Z in Healthy UK Volunteers

TypeinterventionalSponsorUniversity of OxfordRan2015 to 2017Enrolled38ConditionsEbola Virus DiseaseArmsMVA-EBO Z, ChAd3-EBO Z
NCT02485912 phase1completednot on this map

A Phase Ib Safety and Immunogenicity Clinical Trial of Heterologous Prime-boost Immunisation With ChAd3-EBO Z and MVA-EBO Z in Healthy Senegalese Adult Volunteers Aged 18-50 Years.

TypeinterventionalSponsorUniversity of OxfordRan2015 to 2016Enrolled40ConditionsEbola Virus DiseaseArmsChAd3-EBO Z, MVA-EBO Z
3 · Its place in the literature

Who cites it

56 citing papers in PubMed, 1 synthesis or guideline pooled it, 83 citations in OpenAlex.

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  8. Developing the next-generation of adenoviral vector vaccines.Human vaccines & immunotherapeutics · 2025
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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

30 authors at 4 institutions in 3 countries.

Navin VenkatramanJenner Institute, University of Oxford, United Kingdom.
Birahim Pierre NdiayeCentre Hospitalier Universitaire le Dantec, Dakar, Senegal.
Georgina BowyerJenner Institute, University of Oxford, United Kingdom.
Djibril WadeCentre Hospitalier Universitaire le Dantec, Dakar, Senegal.
Saranya SridharJenner Institute, University of Oxford, United Kingdom.
Daniel WrightJenner Institute, University of Oxford, United Kingdom.
Jonathan PowlsonJenner Institute, University of Oxford, United Kingdom.
Ibrahima NdiayeCentre Hospitalier Universitaire le Dantec, Dakar, Senegal.
Siry DièyeCentre Hospitalier Universitaire le Dantec, Dakar, Senegal.
Craig ThompsonJenner Institute, University of Oxford, United Kingdom.
Momar BakhoumCentre Hospitalier Universitaire le Dantec, Dakar, Senegal.
Richard MorterJenner Institute, University of Oxford, United Kingdom.
Stefania CaponeReiThera Srl, Rome, Italy.
Mariarosaria Del SorboReiThera Srl, Rome, Italy.
Sophie JamiesonJenner Institute, University of Oxford, United Kingdom.
Tommy RamplingJenner Institute, University of Oxford, United Kingdom.
Mehreen DatooJenner Institute, University of Oxford, United Kingdom.
Rachel RobertsJenner Institute, University of Oxford, United Kingdom.
Ian PoultonJenner Institute, University of Oxford, United Kingdom.
Oliver GriffithsJenner Institute, University of Oxford, United Kingdom.
W Ripley BallouGlaxoSmithKline Biologicals, Rixensart, Belgium.
François RomanGlaxoSmithKline Biologicals, Rixensart, Belgium.
David J M LewisNational Institute for Health Research/Imperial Clinical Research Facility, Hammersmith Hospital, London, United Kingdom.
Alison LawrieJenner Institute, University of Oxford, United Kingdom.
Egeruan ImoukhuedeJenner Institute, University of Oxford, United Kingdom.
Sarah C GilbertJenner Institute, University of Oxford, United Kingdom.
Tandakha N DieyeCentre Hospitalier Universitaire le Dantec, Dakar, Senegal.
Katie J EwerJenner Institute, University of Oxford, United Kingdom.
Souleymane MboupCentre Hospitalier Universitaire le Dantec, Dakar, Senegal.
Adrian V S HillJenner Institute, University of Oxford, United Kingdom.
University of Oxford · GBHôpital Aristide Le Dantec · SNGlaxoSmithKline (Belgium) · BEHammersmith Hospital · GB

Funding

Department of HealthMedical Research Council MR/R005850/1Wellcome Trust
6 · The paper itself

Abstract

backgroundThe 2014 West African outbreak of Ebola virus disease highlighted the urgent need to develop an effective Ebola vaccine.

methodsWe undertook 2 phase 1 studies assessing safety and immunogenicity of the viral vector modified vaccinia Ankara virus vectored Ebola Zaire vaccine (MVA-EBO-Z), manufactured rapidly on a new duck cell line either alone or in a heterologous prime-boost regimen with recombinant chimpanzee adenovirus type 3 vectored Ebola Zaire vaccine (ChAd3-EBO-Z) followed by MVA-EBO-Z. Adult volunteers in the United Kingdom (n = 38) and Senegal (n = 40) were vaccinated and an accelerated 1-week prime-boost regimen was assessed in Senegal. Safety was assessed by active and passive collection of local and systemic adverse events.

resultsThe standard and accelerated heterologous prime-boost regimens were well-tolerated and elicited potent cellular and humoral immunogenicity in the United Kingdom and Senegal, but vaccine-induced antibody responses were significantly lower in Senegal. Cellular immune responses measured by flow cytometry were significantly greater in African vaccinees receiving ChAd3 and MVA vaccines in the same rather than the contralateral limb.

conclusionsMVA biomanufactured on an immortalized duck cell line shows potential for very large-scale manufacturing with lower cost of goods. This first trial of MVA-EBO-Z in humans encourages further testing in phase 2 studies, with the 1-week prime-boost interval regimen appearing to be particularly suitable for outbreak control. CLINICAL TRIALS REGISTRATION: NCT02451891; NCT02485912.

Indexed as

AdolescentAdultEbola VaccinesEbolavirusFemaleHumansImmunization ScheduleImmunization, SecondaryMaleMiddle AgedSenegalUnited KingdomYoung AdultEbola VaccinesChAd3EbolaMVA; EBO-Zvaccineviral vectors

Identifiers

PMID30407513
PMCPMC6452431
OpenAlexW2903311535

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

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.