Evidence map›Paper›PMID 39643623›Full record

ArticleNPJ vaccines2024

Identifying Plasmodium P36 and P52 antigens for coadministration with circumsporozoite protein to enhance vaccine efficacy.

Naveen Yadav, Anya C Kalata, Rebekah A Reynolds, Andrew Raappana, D Noah Sather, Sean C Murphy

Abstract read
In one paragraph

Article in NPJ vaccines, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
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

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors.

Naveen YadavDepartment of Laboratory Medicine and Pathology, University of Washington, Seattle, WA, USA.
Anya C KalataDepartment of Laboratory Medicine and Pathology, University of Washington, Seattle, WA, USA.
Rebekah A ReynoldsDepartment of Laboratory Medicine and Pathology, University of Washington, Seattle, WA, USA.
Andrew RaappanaCenter for Global Infectious Disease Research, Seattle Children's Research Institute, Seattle, USA.
D Noah SatherCenter for Global Infectious Disease Research, Seattle Children's Research Institute, Seattle, USA.ORCID http://orcid.org/0000-0002-9128-172X
Sean C MurphyDepartment of Laboratory Medicine and Pathology, University of Washington, Seattle, WA, USA. murphysc@uw.edu.ORCID http://orcid.org/0000-0002-2048-0131

Funding

Liver resident memory for malariaR01AI141857 · NIAID · UNIVERSITY OF WASHINGTON · PI MURPHY, SEAN C · 2019 to 2023
$3.9M
NIAID NIH HHS R01 AI141857U.S. Department of Health & Human Services | NIH | National Institute of Allergy and Infectious Diseases (NIAID) 1R01AI141857
6 · The paper itself

Abstract

Vaccines targeting the complex pre-erythrocytic stage of Plasmodium parasites may benefit from the inclusion of multiple antigens. However, discerning protective effects can be difficult because newer candidates may not be as protective as leading antigens like the circumsporozoite protein (CSP) in the conventional pre-clinical mouse model. We developed a modified mouse model challenge strategy that maximizes the contribution of T cells induced by novel candidate antigens at the sporozoite challenge time point and used this approach to test Plasmodium P36 and P52 vaccine candidates alone and in concert with non-protective doses of CSP. Co-administration of P36 and/or P52 with CSP achieved 80-100% sterile protection in mice, compared to only 7-30% protection for each individual antigen. P36 and P52 vaccination induced murine CD4

Identifiers

PMID39643623
PMCPMC11624287

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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.