Evidence map›Paper›PMID 32359873›Full record

ReviewTrends in parasitology2020

The RH5-CyRPA-Ripr Complex as a Malaria Vaccine Target.

Robert J Ragotte, Matthew K Higgins, Simon J Draper

Open access · hybridAbstract readReview
In one paragraph

Review in Trends in parasitology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 49 papers.

0numbers the graph read from it
0cells of the map it votes in
49citing papers in PubMed
8.8field-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

49 citing papers in PubMed, 87 citations in OpenAlex.

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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

3 authors at 1 institution in 1 country.

Robert J RagotteThe Jenner Institute, University of Oxford, Oxford, OX3 7DQ, UK. Electronic address: robert.ragotte@seh.ox.ac.uk.
Matthew K HigginsDepartment of Biochemistry, University of Oxford, Oxford OX1 3QU, UK.
Simon J DraperThe Jenner Institute, University of Oxford, Oxford, OX3 7DQ, UK. Electronic address: simon.draper@ndm.ox.ac.uk.
University of Oxford · GB

Funding

Wellcome Trust
6 · The paper itself

Abstract

Despite ongoing efforts, a highly effective vaccine against Plasmodium falciparum remains elusive. Vaccines targeting the pre-erythrocytic stages of the P. falciparum life cycle are the most advanced to date, affording moderate levels of efficacy in field trials. However, the discovery that the members of the merozoite PfRH5-PfCyRPA-PfRipr (RCR) complex are capable of inducing strain-transcendent neutralizing antibodies has renewed enthusiasm for the possibility of preventing disease by targeting the parasite during the blood stage of infection. With Phase I/II clinical trials now underway using first-generation vaccines against PfRH5, and more on the horizon for PfCyRPA and PfRipr, this review explores the rationale and future potential of the RCR complex as a P. falciparum vaccine target.

Indexed as

Antibodies, NeutralizingAntigens, ProtozoanCarrier ProteinsClinical Trials as TopicMalariaMalaria VaccinesPlasmodium falciparumProtozoan ProteinsAntibodies, NeutralizingAntigens, ProtozoanCarrier ProteinsCyRPA protein, Plasmodium falciparumMalaria VaccinesProtozoan ProteinsRH5 protein, Plasmodium falciparumRipr protein, Plasmodium falciparumCyRPAerythrocyte invasionmalaria vaccinePlasmodium falciparumRH5Ripr

Identifiers

PMID32359873
PMCPMC7246332
OpenAlexW3022853859

What OpenQuestion holds

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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.