Evidence map›Paper›PMID 29213269›Full record

ArticleFrontiers in immunology2017

Safety and Immunogenicity of Malaria Vectored Vaccines Given with Routine Expanded Program on Immunization Vaccines in Gambian Infants and Neonates: A Randomized Controlled Trial.

Victorine A Mensah, Sophie Roetynck, Ebrima K Kanteh, Georgina Bowyer, Amy Ndaw, Francis Oko, Carly M Bliss, Ya Jankey Jagne, Riccardo Cortese, Alfredo Nicosia and 15 more

Registry-linked trialOpen access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT02083887 (A Phase I Study to Assess the Safety and Immunogenicity of ChAd63 ME-TRAP - MVA ME-TRAP Heterologous Prime-boost Vaccination Co-administered With EPI Vaccines in Gambian Infants), which is not on this map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
4.0field-weighted citation impact, top 6% 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.

NCT02083887 phase1completednot on this map

A Phase I Study to Assess the Safety and Immunogenicity of ChAd63 ME-TRAP - MVA ME-TRAP Heterologous Prime-boost Vaccination Co-administered With EPI Vaccines in Gambian Infants

TypeinterventionalSponsorUniversity of OxfordRan2014 to 2015Enrolled65ConditionsMalariaArmsChAd63 ME-TRAP / MVA ME-TRAP
3 · Its place in the literature

Who cites it

19 citing papers in PubMed, 27 citations in OpenAlex.

  1. Trial
  2. Safety and Differential Antibody and T-Cell Responses to theThe American journal of tropical medicine and hygiene · 2019
    Trial
  3. Trial
  4. Trial
  5. Article
  6. Review
  7. Adenovirus-based vaccines-a platform for pandemic preparedness against emerging viral pathogens.Molecular therapy : the journal of the American Society of Gene Therapy · 2022
    Review
  8. Article
  9. Article
  10. Review
  11. Targeting Antigen to the Surface of EVs Improves theMolecular therapy. Methods & clinical development · 2020
    Article
  12. Review
  13. Review
  14. Review
  15. Review
  16. Article
  17. Article
  18. Review
  19. Novel Strategies for Malaria Vaccine Design.Frontiers in immunology · 2018
    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

25 authors at 8 institutions in 5 countries.

Victorine A MensahUniversité Cheikh Anta Diop, Dakar, Senegal.
Sophie RoetynckMedical Research Council Unit, Fajara, Gambia.
Ebrima K KantehMedical Research Council Unit, Fajara, Gambia.
Georgina BowyerThe Jenner Institute Laboratories, University of Oxford, Oxford, United Kingdom.
Amy NdawUniversité Cheikh Anta Diop, Dakar, Senegal.
Francis OkoMedical Research Council Unit, Fajara, Gambia.
Carly M BlissThe Jenner Institute Laboratories, University of Oxford, Oxford, United Kingdom.
Ya Jankey JagneMedical Research Council Unit, Fajara, Gambia.
Riccardo CorteseKeires AG, Basel, Switzerland.
Alfredo NicosiaReiThera, Rome, Italy.
Rachel RobertsCentre for Clinical Vaccinology and Tropical Medicine, The Jenner Institute, Churchill Hospital, Oxford, United Kingdom.
Flavia D'AlessioEuropean Vaccine Initiative, UniversitätsKlinikum Heidelberg, Heidelberg, Germany.
Odile LeroyEuropean Vaccine Initiative, UniversitätsKlinikum Heidelberg, Heidelberg, Germany.
Babacar FayeUniversité Cheikh Anta Diop, Dakar, Senegal.
Beate KampmannMedical Research Council Unit, Fajara, Gambia.
Badara CisseUniversité Cheikh Anta Diop, Dakar, Senegal.
Kalifa BojangMedical Research Council Unit, Fajara, Gambia.
Stephen GerryCentre for Statistics in Medicine, Botnar Research Centre, Nuffield Department of Orthopaedics, Rheumatology and Musculoskeletal Sciences, University of Oxford, Oxford, United Kingdom.
Nicola K ViebigEuropean Vaccine Initiative, UniversitätsKlinikum Heidelberg, Heidelberg, Germany.
Alison M LawrieCentre for Clinical Vaccinology and Tropical Medicine, The Jenner Institute, Churchill Hospital, Oxford, United Kingdom.
Ed ClarkeMedical Research Council Unit, Fajara, Gambia.
Egeruan B ImoukhuedeCentre for Clinical Vaccinology and Tropical Medicine, The Jenner Institute, Churchill Hospital, Oxford, United Kingdom.
Katie J EwerThe Jenner Institute Laboratories, University of Oxford, Oxford, United Kingdom.
Adrian V S HillThe Jenner Institute Laboratories, University of Oxford, Oxford, United Kingdom.
Muhammed O AfolabiMedical Research Council Unit, Fajara, Gambia.
MRC Unit the Gambia · GMCheikh Anta Diop University · SNUniversity of Oxford · GBChurchill Hospital · GBUniversity Hospital Heidelberg · DECeinge Biotecnologie Avanzate (Italy) · ITHeidelberg University · DEJenner Institute · GB

Funding

Medical Research Council MC_UP_A900_1118Medical Research Council MC_UP_A900_1122Medical Research Council MR/R005990/1
6 · The paper itself

Abstract

backgroundHeterologous prime-boost vaccination with chimpanzee adenovirus 63 (ChAd63) and modified vaccinia virus Ankara (MVA) encoding multiple epitope string thrombospondin-related adhesion protein (ME-TRAP) has shown acceptable safety and promising immunogenicity in African adult and pediatric populations. If licensed, this vaccine could be given to infants receiving routine childhood immunizations. We therefore evaluated responses to ChAd63 MVA ME-TRAP when co-administered with routine Expanded Program on Immunization (EPI) vaccines.

methodsWe enrolled 65 Gambian infants and neonates, aged 16, 8, or 1 week at first vaccination and randomized them to receive either ME-TRAP and EPI vaccines or EPI vaccines only. Safety was assessed by the description of vaccine-related adverse events (AEs). Immunogenicity was evaluated using IFNγ enzyme-linked immunospot, whole-blood flow cytometry, and anti-TRAP IgG ELISA. Serology was performed to confirm all infants achieved protective titers to EPI vaccines.

resultsThe vaccines were well tolerated in all age groups with no vaccine-related serious AEs. High-level TRAP-specific IgG and T cell responses were generated after boosting with MVA. CD8

conclusionMalaria vectored prime-boost vaccines co-administered with routine childhood immunizations were well tolerated. Potent humoral and cellular immunity induced by ChAd63 MVA ME-TRAP did not reduce the immunogenicity of co-administered EPI vaccines, supporting further evaluation of this regimen in infant populations. CLINICAL

trial registrationThe clinical trial was registered on http://Clinicaltrials.gov (NCT02083887) and the Pan-African Clinical Trials Registry (PACTR201402000749217).

Indexed as

cellular immune responseclinical trialscytokinesmalariavaccines

Identifiers

PMID29213269
PMCPMC5702785
OpenAlexW2769429855

What OpenQuestion holds

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LicenceCC BY
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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.