Evidence map›Paper›PMID 27185785›Full record

ArticleInfection and immunity2016

Merozoite Antigens of Plasmodium falciparum Elicit Strain-Transcending Opsonizing Immunity.

Danika L Hill, Danny W Wilson, Natalia G Sampaio, Emily M Eriksson, Victoria Ryg-Cornejo, G L Abby Harrison, Alessandro D Uboldi, Leanne J Robinson, James G Beeson, Peter Siba and 4 more

Open access · bronzeAbstract read
In one paragraph

Article in Infection and immunity, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
6.7field-weighted citation impact, top 3% 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

30 citing papers in PubMed, 48 citations in OpenAlex.

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  15. Naturally Acquired Humoral Immunity AgainstFrontiers in immunology · 2020
    Review
  16. Immunization with full-lengthNPJ vaccines · 2020
    Article
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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

14 authors at 5 institutions in 3 countries.

Danika L HillThe Walter and Eliza Hall Institute of Medical Research, Parkville, Australia danika.hill@babraham.ac.uk.
Danny W WilsonThe Walter and Eliza Hall Institute of Medical Research, Parkville, Australia.
Natalia G SampaioThe Walter and Eliza Hall Institute of Medical Research, Parkville, Australia.
Emily M ErikssonThe Walter and Eliza Hall Institute of Medical Research, Parkville, Australia.
Victoria Ryg-CornejoThe Walter and Eliza Hall Institute of Medical Research, Parkville, Australia.
G L Abby HarrisonThe Walter and Eliza Hall Institute of Medical Research, Parkville, Australia.
Alessandro D UboldiThe Walter and Eliza Hall Institute of Medical Research, Parkville, Australia.
Leanne J RobinsonThe Walter and Eliza Hall Institute of Medical Research, Parkville, Australia.
James G BeesonThe Burnet Institute for Medical Research and Public Health, Melbourne, Australia.
Peter SibaPapua New Guinea Institute of Medical Research, Goroka and Madang, Papua New Guinea.
Alan F CowmanThe Walter and Eliza Hall Institute of Medical Research, Parkville, Australia.
Diana S HansenThe Walter and Eliza Hall Institute of Medical Research, Parkville, Australia.
Ivo MuellerThe Walter and Eliza Hall Institute of Medical Research, Parkville, Australia.
Louis SchofieldThe Walter and Eliza Hall Institute of Medical Research, Parkville, Australia.
Walter and Eliza Hall Institute of Medical Research · AUUniversity of Melbourne · AUBarcelona Institute for Global Health · ESBurnet Institute · AUPapua New Guinea Institute of Medical Research · PG

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

It is unclear whether naturally acquired immunity to Plasmodium falciparum results from the acquisition of antibodies to multiple, diverse antigens or to fewer, highly conserved antigens. Moreover, the specific antibody functions required for malaria immunity are unknown, and hence informative immunological assays are urgently needed to address these knowledge gaps and guide vaccine development. In this study, we investigated whether merozoite-opsonizing antibodies are associated with protection from malaria in a strain-specific or strain-transcending manner by using a novel field isolate and an immune plasma-matched cohort from Papua New Guinea with our validated assay of merozoite phagocytosis. Highly correlated opsonization responses were observed across the 15 parasite strains tested, as were strong associations with protection (composite phagocytosis score across all strains in children uninfected at baseline: hazard ratio of 0.15, 95% confidence interval of 0.04 to 0.63). Opsonizing antibodies had a strong strain-transcending component, and the opsonization of transgenic parasites deficient for MSP3, MSP6, MSPDBL1, or P. falciparum MSP1-19 (PfMSP1-19) was similar to that of wild-type parasites. We have provided the first evidence that merozoite opsonization is predominantly strain transcending, and the highly consistent associations with protection against diverse parasite strains strongly supports the use of merozoite opsonization as a correlate of immunity for field studies and vaccine trials. These results demonstrate that conserved domains within merozoite antigens targeted by opsonization generate strain-transcending immune responses and represent promising vaccine candidates.

Indexed as

AdolescentAntibodies, ProtozoanAntigens, ProtozoanChildChild, PreschoolHumansMalaria, FalciparumMerozoitesOpsonin ProteinsPatient Outcome AssessmentPhagocytosisPlasmodium falciparumAntibodies, ProtozoanAntigens, ProtozoanOpsonin Proteins

Identifiers

PMID27185785
PMCPMC4962632
OpenAlexW2398048870

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.