Evidence map›Paper›PMID 28614791›Full record

ArticleJCI insight2017

Human vaccination against Plasmodium vivax Duffy-binding protein induces strain-transcending antibodies.

Ruth O Payne, Sarah E Silk, Sean C Elias, Kathryn H Milne, Thomas A Rawlinson, David Llewellyn, A Rushdi Shakri, Jing Jin, Geneviève M Labbé, Nick J Edwards and 17 more

Registry-linked trialOpen access · goldAbstract read
In one paragraph

Article in JCI insight, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT01816113 (A Phase Ia Clinical Trial to Assess the Safety and Immunogenicity of New Plasmodium Vivax Malaria Vaccine Candidates ChAd63 PvDBP Alone and With MVA PvDBP), which is not on this map. Cited by 67 papers.

0numbers the graph read from it
0cells of the map it votes in
67citing papers in PubMed
9.4field-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.

NCT01816113 phase1completednot on this map

A Phase Ia Clinical Trial to Assess the Safety and Immunogenicity of New Plasmodium Vivax Malaria Vaccine Candidates ChAd63 PvDBP Alone and With MVA PvDBP

TypeinterventionalSponsorUniversity of OxfordRan2013 to 2014Enrolled24ConditionsMalaria, Plasmodium VivaxArmsChAd63 PvDBP 5 x 10^9, ChAd63 PvDBP 5 x 10^10, MVA PvDBP 1 x 10^8, MVA PvDBP 2 x 10^8
3 · Its place in the literature

Who cites it

67 citing papers in PubMed, 101 citations in OpenAlex.

  1. Trial
  2. Trial
  3. Trial
  4. Article
  5. Article
  6. Article
  7. Review
  8. Developing the next-generation of adenoviral vector vaccines.Human vaccines & immunotherapeutics · 2025
    Review
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Review
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  18. Review
  19. Article
  20. Article

7 more citing papers are in PubMed but not listed here.

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

27 authors at 7 institutions in 5 countries.

Ruth O PayneThe Jenner Institute, University of Oxford, Oxford, United Kingdom.
Sarah E SilkThe Jenner Institute, University of Oxford, Oxford, United Kingdom.
Sean C EliasThe Jenner Institute, University of Oxford, Oxford, United Kingdom.
Kathryn H MilneThe Jenner Institute, University of Oxford, Oxford, United Kingdom.
Thomas A RawlinsonThe Jenner Institute, University of Oxford, Oxford, United Kingdom.
David LlewellynThe Jenner Institute, University of Oxford, Oxford, United Kingdom.
A Rushdi ShakriInternational Center for Genetic Engineering and Biotechnology, Aruna Asaf Ali Marg, New Delhi, India.
Jing JinThe Jenner Institute, University of Oxford, Oxford, United Kingdom.
Geneviève M LabbéThe Jenner Institute, University of Oxford, Oxford, United Kingdom.
Nick J EdwardsThe Jenner Institute, University of Oxford, Oxford, United Kingdom.
Ian D PoultonThe Jenner Institute, University of Oxford, Oxford, United Kingdom.
Rachel RobertsThe Jenner Institute, University of Oxford, Oxford, United Kingdom.
Ryan FaridQIMR Berghofer Medical Research Institute, Herston, Queensland, Australia.
Thomas JørgensenExpreS2, ion Biotechnologies, SCION-DTU Science Park, Hørsholm, Denmark.
Daniel Gw AlanineThe Jenner Institute, University of Oxford, Oxford, United Kingdom.
Simone C de CassanThe Jenner Institute, University of Oxford, Oxford, United Kingdom.
Matthew K HigginsDepartment of Biochemistry, University of Oxford, Oxford, United Kingdom.
Thomas D OttoWellcome Trust Sanger Institute, Cambridge, United Kingdom.
James S McCarthyQIMR Berghofer Medical Research Institute, Herston, Queensland, Australia.
Willem A de JonghExpreS2, ion Biotechnologies, SCION-DTU Science Park, Hørsholm, Denmark.
Alfredo NicosiaReiThera SRL (formerly Okairòs SRL), Viale Città d'Europa, Rome, Italy.
Sarah MoyleClinical Biomanufacturing Facility, University of Oxford, Oxford, United Kingdom.
Adrian Vs HillThe Jenner Institute, University of Oxford, Oxford, United Kingdom.
Eleanor BerrieClinical Biomanufacturing Facility, University of Oxford, Oxford, United Kingdom.
Chetan E ChitnisInternational Center for Genetic Engineering and Biotechnology, Aruna Asaf Ali Marg, New Delhi, India.
Alison M LawrieThe Jenner Institute, University of Oxford, Oxford, United Kingdom.
Simon J DraperThe Jenner Institute, University of Oxford, Oxford, United Kingdom.
University of Oxford · GBJenner Institute · GBExpreS2ion Biotechnologies (Denmark) · DKInternational Centre for Genetic Engineering and Biotechnology · INQIMR Berghofer Medical Research Institute · AUUniversity of Naples Federico II · ITWellcome Sanger Institute · GB

Funding

Medical Research Council G1100086Wellcome Trust
6 · The paper itself

Abstract

backgroundPlasmodium vivax is the most widespread human malaria geographically; however, no effective vaccine exists. Red blood cell invasion by the P. vivax merozoite depends on an interaction between the Duffy antigen receptor for chemokines (DARC) and region II of the parasite's Duffy-binding protein (PvDBP_RII). Naturally acquired binding-inhibitory antibodies against this interaction associate with clinical immunity, but it is unknown whether these responses can be induced by human vaccination.

methodsSafety and immunogenicity of replication-deficient chimpanzee adenovirus serotype 63 (ChAd63) and modified vaccinia virus Ankara (MVA) viral vectored vaccines targeting PvDBP_RII (Salvador I strain) were assessed in an open-label dose-escalation phase Ia study in 24 healthy UK adults. Vaccines were delivered by the intramuscular route in a ChAd63-MVA heterologous prime-boost regimen using an 8-week interval.

resultsBoth vaccines were well tolerated and demonstrated a favorable safety profile in malaria-naive adults. PvDBP_RII-specific ex-vivo IFN-γ T cell, antibody-secreting cell, memory B cell, and serum IgG responses were observed after the MVA boost immunization. Vaccine-induced antibodies inhibited the binding of vaccine homologous and heterologous variants of recombinant PvDBP_RII to the DARC receptor, with median 50% binding-inhibition titers greater than 1:100.

conclusionWe have demonstrated for the first time to our knowledge that strain-transcending antibodies can be induced against the PvDBP_RII antigen by vaccination in humans. These vaccine candidates warrant further clinical evaluation of efficacy against the blood-stage P. vivax parasite.

trial registrationClinicaltrials.gov NCT01816113.

fundingSupport was provided by the UK Medical Research Council, UK National Institute of Health Research Oxford Biomedical Research Centre, and the Wellcome Trust.

Indexed as

Infectious diseaseVaccines

Identifiers

PMID28614791
PMCPMC5470884
OpenAlexW2626760342

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.