Evidence map›Paper›PMID 40018046›Full record

ArticleFrontiers in immunology2025

Novel mRNA vaccines induce potent immunogenicity and afford protection against tuberculosis.

Christopher J De Voss, Marcellus Korompis, Shuailin Li, Alberta Ateere, Helen McShane, Elena Stylianou

Abstract read
In one paragraph

Article in Frontiers in immunology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing 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

13 citing papers in PubMed.

  1. Review
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  5. Article
  6. Immunodominant Tuberculosis Antigens Recognized by Human CD4Cold Spring Harbor perspectives in medicine · 2026
    Article
  7. Review
  8. Review
  9. Article
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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

6 authors.

Christopher J De Voss *The Jenner Institute, University of Oxford, Oxford, United Kingdom.
Marcellus Korompis *The Jenner Institute, University of Oxford, Oxford, United Kingdom.
Shuailin LiThe Jenner Institute, University of Oxford, Oxford, United Kingdom.
Alberta AteereThe Jenner Institute, University of Oxford, Oxford, United Kingdom.
Helen McShaneThe Jenner Institute, University of Oxford, Oxford, United Kingdom.
Elena StylianouThe Jenner Institute, University of Oxford, Oxford, United Kingdom.

Funding

Wellcome Trust
6 · The paper itself

Abstract

Introduction: Methods: We selected five Results: Each mRNA construct demonstrated unique cellular and humoral immunogenicity, and both m-Mix, as well as the single antigen EsxI, conferred significant protection in a murine Discussion: This work warrants further investigation of LNP-formulated mRNA vaccines for TB, whilst indicating the potential of m-Mix and C-m-Mix to progress to further stages of vaccine development.

Indexed as

Antigens, BacterialImmunogenicity, VaccinemRNA VaccinesMycobacterium tuberculosisRNA, MessengerTuberculosisTuberculosis VaccinesAnimalsAntibodies, BacterialDisease Models, AnimalFemaleLiposomesMiceMice, Inbred C57BLNanoparticlesVaccines, SyntheticAntibodies, BacterialAntigens, BacterialLipid NanoparticlesLiposomesmRNA VaccinesRNA, MessengerTuberculosis VaccinesVaccines, SyntheticBCGmRNAtuberculosisvaccinesviral-vector

Identifiers

PMID40018046
PMCPMC11865049

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.