Evidence map›Paper›PMID 24930599›Full record

ArticleMolecular therapy : the journal of the American Society of Gene Therapy2014

Translating the immunogenicity of prime-boost immunization with ChAd63 and MVA ME-TRAP from malaria naive to malaria-endemic populations.

Domtila Kimani, Ya Jankey Jagne, Momodou Cox, Eva Kimani, Carly M Bliss, Evelyn Gitau, Caroline Ogwang, Muhammed O Afolabi, Georgina Bowyer, Katharine A Collins and 26 more

Open access · bronzeAbstract readClinical Trial, Phase I
In one paragraph

Article in Molecular therapy : the journal of the American Society of Gene Therapy, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed, 1 pooled it
9.6field-weighted citation impact, top 2% 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

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

  1. Pooled it
  2. Trial
  3. Trial
  4. Trial
  5. Trial
  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
  7. Trial
  8. Trial
  9. Trial
  10. Trial
  11. Review
  12. Article
  13. Review
  14. Article
  15. High-throughput single-сell sequencing in cancer research.Signal transduction and targeted therapy · 2022
    Review
  16. Article
  17. Article
  18. Vaccines: Underlying Principles of Design and Testing.Clinical pharmacology and therapeutics · 2021
    Article
  19. 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

36 authors at 8 institutions in 6 countries.

Domtila KimaniKenya Medical Research Institute, Centre for Geographical Medical Research (Coast), Kilifi, Kenya.
Ya Jankey JagneMedical Research Council Unit, Fajara, The Gambia.
Momodou CoxMedical Research Council Unit, Fajara, The Gambia.
Eva KimaniKenya Medical Research Institute, Centre for Geographical Medical Research (Coast), Kilifi, Kenya.
Carly M BlissThe Jenner Institute Laboratories, University of Oxford, Oxford, UK.
Evelyn GitauKenya Medical Research Institute, Centre for Geographical Medical Research (Coast), Kilifi, Kenya.
Caroline OgwangKenya Medical Research Institute, Centre for Geographical Medical Research (Coast), Kilifi, Kenya.
Muhammed O AfolabiMedical Research Council Unit, Fajara, The Gambia.
Georgina BowyerThe Jenner Institute Laboratories, University of Oxford, Oxford, UK.
Katharine A CollinsThe Jenner Institute Laboratories, University of Oxford, Oxford, UK.
Nick EdwardsThe Jenner Institute Laboratories, University of Oxford, Oxford, UK.
Susanne H HodgsonCentre for Clinical Vaccinology and Tropical Medicine, The Jenner Institute, Churchill Hospital, Oxford, UK.
Christopher J A DuncanCentre for Clinical Vaccinology and Tropical Medicine, The Jenner Institute, Churchill Hospital, Oxford, UK.
Alexandra J SpencerThe Jenner Institute Laboratories, University of Oxford, Oxford, UK.
Miguel G KnightKenya Medical Research Institute, Centre for Geographical Medical Research (Coast), Kilifi, Kenya.
Abdoulie DrammehMedical Research Council Unit, Fajara, The Gambia.
Nicholas A AnagnostouCentre for Clinical Vaccinology and Tropical Medicine, The Jenner Institute, Churchill Hospital, Oxford, UK.
Eleanor BerrieClinical Biomanufacturing Facility, University of Oxford, Churchill Hospital, Oxford, UK.
Sarah MoyleClinical Biomanufacturing Facility, University of Oxford, Churchill Hospital, Oxford, UK.
Sarah C GilbertThe Jenner Institute Laboratories, University of Oxford, Oxford, UK.
Peninah SoipeiKenya Medical Research Institute, Centre for Geographical Medical Research (Coast), Kilifi, Kenya.
Joseph OkebeMedical Research Council Unit, Fajara, The Gambia.
Stefano CollocaOkairòs AG, Rome, Italy.
Riccardo Cortese1] Okairòs AG, Rome, Italy [2] CEINGE, Naples, Italy.
Nicola K ViebigEuropean Vaccine Initiative, UniversitätsKlinikum Heidelberg, Heidelberg, Germany.
Rachel RobertsCentre for Clinical Vaccinology and Tropical Medicine, The Jenner Institute, Churchill Hospital, Oxford, UK.
Alison M LawrieCentre for Clinical Vaccinology and Tropical Medicine, The Jenner Institute, Churchill Hospital, Oxford, UK.
Alfredo Nicosia1] Okairòs AG, Rome, Italy [2] CEINGE, Naples, Italy [3] Department of Biochemistry and Medical Biotechnology, University Federico II Naples, Naples, Italy.
Egeruan B ImoukhuedeEuropean Vaccine Initiative, UniversitätsKlinikum Heidelberg, Heidelberg, Germany.
Philip BejonKenya Medical Research Institute, Centre for Geographical Medical Research (Coast), Kilifi, Kenya.
Roma ChilengiKenya Medical Research Institute, Centre for Geographical Medical Research (Coast), Kilifi, Kenya.
Kalifa BojangMedical Research Council Unit, Fajara, The Gambia.
Katie L Flanagan1] Medical Research Council Unit, Fajara, The Gambia [2] Department of Immunology, Monash University, Melbourne, Australia.
Adrian V S Hill1] The Jenner Institute Laboratories, University of Oxford, Oxford, UK [2] Centre for Clinical Vaccinology and Tropical Medicine, The Jenner Institute, Churchill Hospital, Oxford, UK.
Britta C Urban1] Kenya Medical Research Institute, Centre for Geographical Medical Research (Coast), Kilifi, Kenya [2] Liverpool School of Tropical Medicine, Liverpool, UK.
Katie J EwerThe Jenner Institute Laboratories, University of Oxford, Oxford, UK.
Jenner Institute · GBKenya Medical Research Institute · KEMRC Unit the Gambia · GMUniversity of Oxford · GBCeinge Biotecnologie Avanzate (Italy) · ITChurchill Hospital · GBUniversity Hospital Heidelberg · DELiverpool School of Tropical Medicine · GB

Funding

Medical Research Council G0502018Medical Research Council MC_UP_A900_1118Wellcome Trust 084113/Z/07/ZWellcome Trust 090532Wellcome Trust 092654Wellcome Trust 095540Wellcome Trust 097940Wellcome Trust 097940/Z/11/Z
6 · The paper itself

Abstract

To induce a deployable level of efficacy, a successful malaria vaccine would likely benefit from both potent cellular and humoral immunity. These requirements are met by a heterologous prime-boost immunization strategy employing a chimpanzee adenovirus vector followed by modified vaccinia Ankara (MVA), both encoding the pre-erythrocytic malaria antigen ME-thrombospondin-related adhesive protein (TRAP), with high immunogenicity and significant efficacy in UK adults. We undertook two phase 1b open-label studies in adults in Kenya and The Gambia in areas of similar seasonal malaria transmission dynamics and have previously reported safety and basic immunogenicity data. We now report flow cytometry and additional interferon (IFN)-γ enzyme-linked immunospot (ELISPOT) data characterizing pre-existing and induced cellular immunity as well as anti-TRAP IgG responses. T-cell responses induced by vaccination averaged 1,254 spot-forming cells (SFC) per million peripheral blood mononuclear cells (PBMC) across both trials and flow cytometry revealed cytokine production from both CD4(+) and CD8(+) T cells with the frequency of CD8(+) IFN-γ-secreting monofunctional T cells (previously shown to associate with vaccine efficacy) particularly high in Kenyan adults. Immunization with ChAd63 and MVA ME-TRAP induced strong cellular and humoral immune responses in adults living in two malaria-endemic regions of Africa. This prime-boost approach targeting the pre-erythrocytic stage of the malaria life-cycle is now being assessed for efficacy in a target population.

Indexed as

Adenoviruses, SimianAdultEndemic DiseasesGambiaHumansImmunization, SecondaryKenyaMalaria, FalciparumMalaria VaccinesProtozoan ProteinsT-LymphocytesUnited KingdomVaccinia virusMalaria VaccinesProtozoan Proteinsthrombospondin-related adhesive protein, protozoan

Identifiers

PMID24930599
PMCPMC4188556
OpenAlexW2002833434

What OpenQuestion holds

Textmetadata
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.