Evidence map›Paper›PMID 30768655›Full record

ArticlePLoS neglected tropical diseases2019

Antibody responses to Plasmodium vivax Duffy binding and Erythrocyte binding proteins predict risk of infection and are associated with protection from clinical Malaria.

Wen-Qiang He, Ahmad Rushdi Shakri, Rukmini Bhardwaj, Camila T França, Danielle I Stanisic, Julie Healer, Benson Kiniboro, Leanne J Robinson, Micheline Guillotte-Blisnick, Christèle Huon and 6 more

Open access · goldAbstract read
In one paragraph

Article in PLoS neglected tropical diseases, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
5.3field-weighted citation impact, top 4% 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

26 citing papers in PubMed, 34 citations in OpenAlex.

  1. Article
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  4. Human genetic variations conferring resistance to malaria.Journal of translational medicine · 2025
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  8. IgM antibody responses againstFrontiers in cellular and infection microbiology · 2023
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  13. Frontiers in immunology · 2022
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  14. Observational
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  17. Progress towards the development of aExpert review of vaccines · 2021
    Review
  18. Article
  19. Article
  20. Article
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

16 authors at 7 institutions in 5 countries.

Wen-Qiang HeInfection and Immunity Division, Walter and Eliza Hall Institute of Medical Research, Parkville, Victoria, Australia.
Ahmad Rushdi ShakriMalaria Group, International Centre for Genetic Engineering and Biotechnology (ICGEB), New Delhi, India.
Rukmini BhardwajMalaria Group, International Centre for Genetic Engineering and Biotechnology (ICGEB), New Delhi, India.
Camila T FrançaDepartment of Medical Biology, University of Melbourne, Melbourne, Australia.
Danielle I StanisicInsitute for Glycomics, Griffith University, Southport, Queensland, Australia.ORCID 0000-0003-3908-7468
Julie HealerInfection and Immunity Division, Walter and Eliza Hall Institute of Medical Research, Parkville, Victoria, Australia.
Benson KiniboroMalaria Immuno-Epidemiology Unit, PNG Institute of Medical Research, Madang, Papua New Guinea.
Leanne J RobinsonPopulation Health and Immunity Division, Walter and Eliza Hall Institute of Medical Research, Parkville, Victoria, Australia.
Micheline Guillotte-BlisnickDepartment of Parasites & Insect Vectors, Institut Pasteur, Paris, France.
Christèle HuonDepartment of Parasites & Insect Vectors, Institut Pasteur, Paris, France.
Peter SibaMalaria Immuno-Epidemiology Unit, PNG Institute of Medical Research, Madang, Papua New Guinea.
Alan CowmanInfection and Immunity Division, Walter and Eliza Hall Institute of Medical Research, Parkville, Victoria, Australia.
Christopher L KingCenter for Global Health & Diseases, Case Western Reserve University, Cleveland, OH, United States of America.
Wai-Hong ThamInfection and Immunity Division, Walter and Eliza Hall Institute of Medical Research, Parkville, Victoria, Australia.
Chetan E ChitnisMalaria Group, International Centre for Genetic Engineering and Biotechnology (ICGEB), New Delhi, India.
Ivo MuellerDepartment of Medical Biology, University of Melbourne, Melbourne, Australia.ORCID 0000-0001-6554-6889
Institut Pasteur · FRThe University of Melbourne · AUInternational Centre for Genetic Engineering and Biotechnology · INPapua New Guinea Institute of Medical Research · PGWalter and Eliza Hall Institute of Medical Research · AUCenter for Global Health · USGriffith University · AU

Funding

Howard Hughes Medical InstituteWellcome Trust 208693/Z/17/Z
6 · The paper itself

Abstract

backgroundThe Plasmodium vivax Duffy Binding Protein (PvDBP) is a key target of naturally acquired immunity. However, region II of PvDBP, which contains the receptor-binding site, is highly polymorphic. The natural acquisition of antibodies to different variants of PvDBP region II (PvDBPII), including the AH, O, P and Sal1 alleles, the central region III-V (PvDBPIII-V), and P. vivax Erythrocyte Binding Protein region II (PvEBPII) and their associations with risk of clinical P. vivax malaria are not well understood. METHODOLOGY: Total IgG and IgG subclasses 1, 2, and 3 that recognize four alleles of PvDBPII (AH, O, P, and Sal1), PvDBPIII-V and PvEBPII were measured in samples collected from a cohort of 1 to 3 year old Papua New Guinean (PNG) children living in a highly endemic area of PNG. The levels of binding inhibitory antibodies (BIAbs) to PvDBPII (AH, O, and Sal1) were also tested in a subset of children. The association of presence of IgG with age, cumulative exposure (measured as the product of age and malaria infections during follow-up) and prospective risk of clinical malaria were evaluated.

resultsThe increase in antigen-specific total IgG, IgG1, and IgG3 with age and cumulative exposure was only observed for PvDBPII AH and PvEBPII. High levels of total IgG and predominant subclass IgG3 specific for PvDBPII AH were associated with decreased incidence of clinical P. vivax episodes (aIRR = 0.56-0.68, P≤0.001-0.021). High levels of total IgG and IgG1 to PvEBPII correlated strongly with protection against clinical vivax malaria compared with IgGs against all PvDBPII variants (aIRR = 0.38, P<0.001). Antibodies to PvDBPII AH and PvEBPII showed evidence of an additive effect, with a joint protective association of 70%.

conclusionAntibodies to the key parasite invasion ligands PvDBPII and PvEBPII are good correlates of protection against P. vivax malaria in PNG. This further strengthens the rationale for inclusion of PvDBPII in a recombinant subunit vaccine for P. vivax malaria and highlights the need for further functional studies to determine the potential of PvEBPII as a component of a subunit vaccine for P. vivax malaria.

Indexed as

Antibody SpecificityAntigens, ProtozoanChild, PreschoolFemaleHumansImmunoglobulin GInfantMalaria, VivaxMalePapua New GuineaParasitemiaProtozoan ProteinsReceptors, Cell SurfaceAntigens, ProtozoanDuffy antigen binding protein, PlasmodiumImmunoglobulin GProtozoan ProteinsReceptors, Cell Surface

Identifiers

PMID30768655
PMCPMC6400399
OpenAlexW2911733880

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Registered trials

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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.