Evidence map›Paper›PMID 29118376›Full record

ArticleScientific reports2017

Novel Plasmodium antigens identified via genome-based antibody screen induce protection associated with polyfunctional T cell responses.

Sophie Schussek, Angela Trieu, Simon H Apte, John Sidney, Alessandro Sette, Denise L Doolan

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
2.7field-weighted citation impact, top 10% 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

10 citing papers in PubMed, 14 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Immune Signature AgainstMolecular & cellular proteomics : MCP · 2020
    Article
  5. Article
  6. Article
  7. Comprehensive Review of HumanFrontiers in immunology · 2019
    Review
  8. Review
  9. Chimeric Murine Polyomavirus Virus-Like Particles InduceFrontiers in cellular and infection microbiology · 2019
    Article
  10. Review
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

6 authors at 3 institutions in 2 countries.

Sophie SchussekQIMR Berghofer Medical Research Institute, Infectious Diseases Programme, Herston, QLD 4006, Australia.
Angela TrieuQIMR Berghofer Medical Research Institute, Infectious Diseases Programme, Herston, QLD 4006, Australia.
Simon H ApteQIMR Berghofer Medical Research Institute, Infectious Diseases Programme, Herston, QLD 4006, Australia.ORCID 0000-0003-3105-0820
John SidneyLa Jolla Institute of Allergy and Immunology, San Diego, CA, 92121, USA.
Alessandro SetteLa Jolla Institute of Allergy and Immunology, San Diego, CA, 92121, USA.
Denise L DoolanQIMR Berghofer Medical Research Institute, Infectious Diseases Programme, Herston, QLD 4006, Australia. Denise.Doolan@jcu.edu.au.
QIMR Berghofer Medical Research Institute · AULa Jolla Institute for Immunology · USThe University of Queensland · AU

Funding

Single-cell atlas of lung tissue-resident memory T cells reactive to upper and lower respiratory tract pathogensU19AI118626 · NIAID · LA JOLLA INSTITUTE FOR IMMUNOLOGY · PI Bjoern Peters · 2015 to 2026
$36.7M
NIAID NIH HHS HHSN272200900044CNIAID NIH HHS U19 AI118626
6 · The paper itself

Abstract

The development of vaccines against complex intracellular pathogens, such as Plasmodium spp., where protection is likely mediated by cellular immune responses, has proven elusive. The availability of whole genome, proteome and transcriptome data has the potential to advance rational vaccine development but yet there are no licensed vaccines against malaria based on antigens identified from genomic data. Here, we show that the Plasmodium yoelii orthologs of four Plasmodium falciparum proteins identified by an antibody-based genome-wide screening strategy induce a high degree of sterile infection-blocking protection against sporozoite challenge in a stringent rodent malaria model. Protection increased in multi-antigen formulations. Importantly, protection was highly correlated with the induction of multifunctional triple-positive T cells expressing high amounts of IFN-γ, IL-2 and TNF. These data demonstrate that antigens identified by serological screening are targets of multifunctional cellular immune responses that correlate with protection. Our results provide experimental validation for the concept of rational vaccine design from genomic sequence data.

Indexed as

Genome, ProtozoanAnimalsAntibodies, ProtozoanAntigens, ProtozoanCytokinesFemaleImmunizationMalariaMalaria VaccinesMice, Inbred BALB CPlasmodiumProteomeProtozoan ProteinsSporozoitesT-LymphocytesAntibodies, ProtozoanAntigens, ProtozoanCytokinesMalaria VaccinesProteomeProtozoan Proteins

Identifiers

PMID29118376
PMCPMC5678182
OpenAlexW2766651677

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.