Evidence map›Paper›PMID 23526949›Full record

Trial reportPloS one2013

Safety and immunogenicity of heterologous prime-boost immunisation with Plasmodium falciparum malaria candidate vaccines, ChAd63 ME-TRAP and MVA ME-TRAP, in healthy Gambian and Kenyan adults.

Caroline Ogwang, Muhammed Afolabi, Domtila Kimani, Ya Jankey Jagne, Susanne H Sheehy, Carly M Bliss, Christopher J A Duncan, Katharine A Collins, Miguel A Garcia Knight, Eva Kimani and 23 more

5 registry-linked trialsOpen access · goldAbstract readClinical Trial, Phase IRandomized Controlled Trial
In one paragraph

Trial report in PloS one, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 5 registered trials, which are not on this map. Cited by 41 papers.

0numbers the graph read from it
0cells of the map it votes in
41citing papers in PubMed
12.4field-weighted citation impact, top 1% 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.

NCT01373879 phase1completednot on this map

Safety and Immunogenicity of Heterologous Prime-boost With the Candidate Malaria Vaccines AdCh63 ME-TRAP and MVA ME-TRAP in Healthy Adults and Children in a Malaria Endemic Area

TypeinterventionalSponsorUniversity of OxfordRan2010 to 2011Enrolled52ConditionsMalariaArmsAdCh63 ME-TRAP, MVA ME-TRAP, HDCRV
NCT01379430 phase1completednot on this map

Safety and Immunogenicity of Heterologous Prime-boost With the Candidate Malaria Vaccines AdCh63 ME-TRAP and MVA ME-TRAP in Healthy Adults in a Malaria Endemic Area

TypeinterventionalSponsorUniversity of OxfordRan2010 to 2011Enrolled30ConditionsMalariaArmsAdCh63 ME-TRAP followed by MVA ME-TRAP
NCT02485912 phase1completednot on this mapstarted 2015, after this paper: background citation

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
NCT02925403 phase1 / phase2completednot on this mapstarted 2016, after this paper: background citation

A Phase Ib Randomised, Controlled, Single-blind Study to Assess the Safety, Immunogenicity of the Malaria Vaccine Candidate R21 With Matrix-M1 Adjuvant in West African Adult Volunteers

TypeinterventionalSponsorUniversity of OxfordRan2016 to 2017Enrolled13ConditionsMalariaArmsR21/Matrix-M1, Saline
NCT03341754 phase1completednot on this mapstarted 2018, after this paper: background citation

A Phase 1 Trial With Controlled Human Malaria Infection to Evaluate the Safety, Immunogenicity, and Protective Efficacy of Two-Antigen and Three-Antigen Plasmodium Falciparum DNA Prime-Adenovirus Boost Malaria Vaccine Regimens in Healthy Malaria Naïve Adults

TypeinterventionalSponsorU.S. Army Medical Research and Development CommandRan2018 to 2020Enrolled52ConditionsMalariaArmsD/ChAd63-CA, D/ChAd63-CAT, Infectivity Control (IC) Group
3 · Its place in the literature

Who cites it

41 citing papers in PubMed, 80 citations in OpenAlex.

  1. Trial
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  6. Safety and Immunogenicity of ChAd63 and MVA ME-TRAP in West African Children and Infants.Molecular therapy : the journal of the American Society of Gene Therapy · 2016
    Trial
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  8. Trial
  9. Trial
  10. Trial
  11. Trial
  12. Trial
  13. Article
  14. Review
  15. Article
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  17. Article
  18. Vaccines: Underlying Principles of Design and Testing.Clinical pharmacology and therapeutics · 2021
    Article
  19. Identification and characterization of protective CD8Immunity, inflammation and disease · 2020
    Article
  20. Review
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

33 authors at 8 institutions in 5 countries.

Caroline OgwangKenya Medical Research Institute, Centre for Geographical Medical Research Coast, Kilifi, Kenya.
Muhammed Afolabi
Domtila Kimani
Ya Jankey Jagne
Susanne H Sheehy
Carly M Bliss
Christopher J A Duncan
Katharine A Collins
Miguel A Garcia Knight
Eva Kimani
Nicholas A Anagnostou
Eleanor Berrie
Sarah Moyle
Sarah C Gilbert
Alexandra J Spencer
Peninah Soipei
Jenny Mueller
Joseph Okebe
Stefano Colloca
Riccardo Cortese
Nicola K Viebig
Rachel Roberts
Katherine Gantlett
Alison M Lawrie
Alfredo Nicosia
Egeruan B Imoukhuede
Philip Bejon
Britta C Urban
Katie L Flanagan
Katie J Ewer
Roma Chilengi
Adrian V S Hill
Kalifa Bojang
Churchill Hospital · GBKenya Medical Research Institute · KEMRC Unit the Gambia · GMJenner Institute · GBUniversity of Oxford · GBCeinge Biotecnologie Avanzate (Italy) · ITVienna Vaccine Safety Initiative · DELiverpool School of Tropical Medicine · GB

Funding

Medical Research Council G0502018Medical Research Council G1002624Medical Research Council MC_UP_A900_1118Wellcome Trust 090532Wellcome Trust 095540
6 · The paper itself

Abstract

backgroundHeterologous prime boost immunization with chimpanzee adenovirus 63 (ChAd63) and Modified vaccinia Virus Ankara (MVA) vectored vaccines is a strategy recently shown to be capable of inducing strong cell mediated responses against several antigens from the malaria parasite. ChAd63-MVA expressing the Plasmodium falciparum pre-erythrocytic antigen ME-TRAP (multiple epitope string with thrombospondin-related adhesion protein) is a leading malaria vaccine candidate, capable of inducing sterile protection in malaria naïve adults following controlled human malaria infection (CHMI). METHODOLOGY: We conducted two Phase Ib dose escalation clinical trials assessing the safety and immunogenicity of ChAd63-MVA ME-TRAP in 46 healthy malaria exposed adults in two African countries with similar malaria transmission patterns.

resultsChAd63-MVA ME-TRAP was shown to be safe and immunogenic, inducing high-level T cell responses (median >1300 SFU/million PBMC).

conclusionsChAd63-MVA ME-TRAP is a safe and highly immunogenic vaccine regimen in adults with prior exposure to malaria. Further clinical trials to assess safety and immunogenicity in children and infants and protective efficacy in the field are now warranted.

trial registrationPactr.org PACTR2010020001771828 Pactr.org PACTR201008000221638 ClinicalTrials.gov NCT01373879 NCT01373879 ClinicalTrials.gov NCT01379430 NCT01379430.

Indexed as

Adenoviruses, SimianAdultAntigens, ProtozoanGambiaGenetic VectorsHumansImmunization, SecondaryInterferon-gammaKenyaMalaria, FalciparumMalaria VaccinesMaleMiddle AgedPlasmodium falciparumT-LymphocytesVaccines, SyntheticAntigens, ProtozoanInterferon-gammaMalaria VaccinesVaccines, Synthetic

Identifiers

PMID23526949
PMCPMC3602521
OpenAlexW1973228533

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.