Evidence map›Paper›PMID 30965383›Full record

ArticleCellular microbiology2019

Neutralising antibodies block the function of Rh5/Ripr/CyRPA complex during invasion of Plasmodium falciparum into human erythrocytes.

Julie Healer, Wilson Wong, Jennifer K Thompson, Wengqiang He, Richard W Birkinshaw, Kazutoyo Miura, Carol A Long, Vladislav Soroka, Teit Max Moscote Søgaard, Thomas Jørgensen and 8 more

Open access · hybridAbstract read
In one paragraph

Article in Cellular microbiology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 40 papers.

0numbers the graph read from it
0cells of the map it votes in
40citing papers in PubMed
6.0field-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

40 citing papers in PubMed, 55 citations in OpenAlex.

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  19. Current approaches to malaria vaccines.Current opinion in microbiology · 2022
    Review
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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

18 authors at 5 institutions in 4 countries.

Julie HealerInfection and Immunity, Walter and Eliza Hall Institute of Medical Research, Melbourne, Victoria, Australia.
Wilson WongInfection and Immunity, Walter and Eliza Hall Institute of Medical Research, Melbourne, Victoria, Australia.
Jennifer K ThompsonInfection and Immunity, Walter and Eliza Hall Institute of Medical Research, Melbourne, Victoria, Australia.
Wengqiang HeInfection and Immunity, Walter and Eliza Hall Institute of Medical Research, Melbourne, Victoria, Australia.
Richard W BirkinshawInfection and Immunity, Walter and Eliza Hall Institute of Medical Research, Melbourne, Victoria, Australia.
Kazutoyo MiuraLaboratory of Malaria and Vector Research, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, Maryland, USA.
Carol A LongLaboratory of Malaria and Vector Research, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, Maryland, USA.
Vladislav SorokaExpreS2ion Biotechnologies, Horsholm, Denmark.
Teit Max Moscote SøgaardExpreS2ion Biotechnologies, Horsholm, Denmark.
Thomas JørgensenExpreS2ion Biotechnologies, Horsholm, Denmark.
Willem A de JonghExpreS2ion Biotechnologies, Horsholm, Denmark.
Christopher WeirInfection and Immunity, Walter and Eliza Hall Institute of Medical Research, Melbourne, Victoria, Australia.
Ella SvahnSchools of Chemistry and Biological Sciences, University of Edinburgh, Edinburgh, Scotland, UK.
Peter E CzabotarInfection and Immunity, Walter and Eliza Hall Institute of Medical Research, Melbourne, Victoria, Australia.
Wai-Hong ThamInfection and Immunity, Walter and Eliza Hall Institute of Medical Research, Melbourne, Victoria, Australia.
Ivo MuellerInfection and Immunity, Walter and Eliza Hall Institute of Medical Research, Melbourne, Victoria, Australia.
Paul N BarlowSchools of Chemistry and Biological Sciences, University of Edinburgh, Edinburgh, Scotland, UK.
Alan F CowmanInfection and Immunity, Walter and Eliza Hall Institute of Medical Research, Melbourne, Victoria, Australia.ORCID 0000-0001-5145-9004
The University of Melbourne · AUExpreS2ion Biotechnologies (Denmark) · DKNational Institutes of Health · USUniversity of Edinburgh · GBWalter and Eliza Hall Institute of Medical Research · AU

Funding

Howard Hughes Medical Institute 55007645Wellcome Trust 208693/Z/17/Z
6 · The paper itself

Abstract

An effective vaccine is a priority for malaria control and elimination. The leading candidate in the Plasmodium falciparum blood stage is PfRh5. PfRh5 assembles into trimeric complex with PfRipr and PfCyRPA in the parasite, and this complex is essential for erythrocyte invasion. In this study, we show that antibodies specific for PfRh5 and PfCyRPA prevent trimeric complex formation. We identify the EGF-7 domain on PfRipr as a neutralising epitope and demonstrate that antibodies against this region act downstream of complex formation to prevent merozoite invasion. Antibodies against the C-terminal region of PfRipr were more inhibitory than those against either PfRh5 or PfCyRPA alone, and a combination of antibodies against PfCyRPA and PfRipr acted synergistically to reduce invasion. This study supports prioritisation of PfRipr for development as part of a next-generation antimalarial vaccine.

Indexed as

Antibodies, NeutralizingAntigens, ProtozoanCarrier ProteinsErythrocytesHumansMalaria, FalciparumMalaria VaccinesMerozoitesPlasmodium falciparumProtozoan ProteinsAntibodies, NeutralizingAntigens, ProtozoanCarrier ProteinsCyRPA protein, Plasmodium falciparumMalaria VaccinesProtozoan ProteinsRH5 protein, Plasmodium falciparumRipr protein, Plasmodium falciparum

Identifiers

PMID30965383
PMCPMC6594224
OpenAlexW2940415435

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.