Evidence map›Paper›PMID 34031479›Full record

ArticleScientific reports2021

Ultra-low dose immunization and multi-component vaccination strategies enhance protection against malaria in mice.

Katharine A Collins, Florian Brod, Rebecca Snaith, Marta Ulaszewska, Rhea J Longley, Ahmed M Salman, Sarah C Gilbert, Alexandra J Spencer, David Franco, W Ripley Ballou and 1 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
2.9field-weighted citation impact, top 9% 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

15 citing papers in PubMed, 21 citations in OpenAlex.

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  6. Immunogenicity evaluation of altSonflex1-2-3Frontiers in immunology · 2025
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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

11 authors at 3 institutions in 2 countries.

Katharine A Collins *Jenner Institute, Nuffield Department of Medicine, University of Oxford, Oxford, UK. Katharine.a.collins@gmail.com.
Florian Brod *Jenner Institute, Nuffield Department of Medicine, University of Oxford, Oxford, UK.
Rebecca SnaithJenner Institute, Nuffield Department of Medicine, University of Oxford, Oxford, UK.
Marta UlaszewskaJenner Institute, Nuffield Department of Medicine, University of Oxford, Oxford, UK.
Rhea J LongleyJenner Institute, Nuffield Department of Medicine, University of Oxford, Oxford, UK.
Ahmed M SalmanJenner Institute, Nuffield Department of Medicine, University of Oxford, Oxford, UK.
Sarah C GilbertJenner Institute, Nuffield Department of Medicine, University of Oxford, Oxford, UK.
Alexandra J SpencerJenner Institute, Nuffield Department of Medicine, University of Oxford, Oxford, UK.
David FrancoGSK Vaccines, Rixensart, Belgium.
W Ripley BallouGSK Vaccines, Rixensart, Belgium.
Adrian V S HillJenner Institute, Nuffield Department of Medicine, University of Oxford, Oxford, UK.
Jenner Institute · GBUniversity of Oxford · GBGlaxoSmithKline (Belgium) · BE

Funding

Wellcome Trust 095540/Z/11/ZWellcome Trust 102051/Z/13/ZWellcome Trust 104750/Z/14/Z
6 · The paper itself

Abstract

An effective vaccine would be a valuable tool for malaria control and elimination; however, the leading malaria vaccine in development, RTS,S/AS01, provided only partial protection in a Phase 3 trial. R21 is a next-generation RTS,S-like vaccine. We have previously shown in mice that R21 administered in Matrix-M is highly immunogenic, able to elicit complete protection against sporozoite challenge, and can be successfully administered with TRAP based viral-vectors resulting in enhanced protection. In this study, we developed a novel, GMP-compatible purification process for R21, and evaluated the immunogenicity and protective efficacy of ultra-low doses of both R21 and RTS,S when formulated in AS01. We demonstrated that both vaccines are highly immunogenic and also elicit comparable high levels of protection against transgenic parasites in BALB/c mice. By lowering the vaccine dose there was a trend for increased immunogenicity and sterile protection, with the highest dose vaccine groups achieving the lowest efficacy (50% sterile protection). We also evaluated the ability to combine RTS,S/AS01 with TRAP based viral-vectors and observed concurrent induction of immune responses to both antigens with minimal interference when mixing the vaccines prior to administration. These studies suggest that R21 or RTS,S could be combined with viral-vectors for a multi-component vaccination approach and indicate that low dose vaccination should be fully explored in humans to maximize potential efficacy.

Indexed as

AnimalsAntibodies, ProtozoanDose-Response Relationship, DrugDrug SynergismFemaleHumansImmunizationMalariaMalaria VaccinesMiceMice, Inbred BALB CMice, TransgenicVaccines, SyntheticVaccines, Virus-Like ParticleAntibodies, ProtozoanMalaria VaccinesRTS,S-AS01 vaccineVaccines, SyntheticVaccines, Virus-Like Particle

Identifiers

PMID34031479
PMCPMC8144388
OpenAlexW3164565931

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.