Evidence map›Paper›PMID 25282504›Full record

ArticleNature chemical biology2014

A self-adjuvanting vaccine induces cytotoxic T lymphocytes that suppress allergy.

Regan J Anderson, Ching-wen Tang, Naomi J Daniels, Benjamin J Compton, Colin M Hayman, Karen A Johnston, Deborah A Knight, Olivier Gasser, Hazel C Poyntz, Peter M Ferguson and 4 more

Abstract read
PubMed Publisher
In one paragraph

Article in Nature chemical biology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
3.7field-weighted citation impact, top 6% 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

31 citing papers in PubMed, 84 citations in OpenAlex.

  1. Article
  2. Review
  3. Development of a Self-Adjuvanting Influenza Peptide-Glycolipid Conjugate Inducing CD8Chembiochem : a European journal of chemical biology · 2026
    Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Glycolipid-peptide conjugate vaccines elicit CD8Clinical & translational immunology · 2022
    Article
  10. Synthetic protein conjugate vaccines provide protection againstProceedings of the National Academy of Sciences of the United States of America · 2021
    Article
  11. Harnessing NKT cells for vaccination.Oxford open immunology · 2021
    Review
  12. Review
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Review
  19. Review
  20. Article
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

14 authors at 4 institutions in 1 country.

Regan J AndersonThe Ferrier Research Institute, Victoria University of Wellington, Wellington, New Zealand.ORCID 0000000334679202
Ching-wen TangMalaghan Institute of Medical Research, Wellington, New Zealand.
Naomi J Daniels1] Malaghan Institute of Medical Research, Wellington, New Zealand. [2] Department of Pathology and Molecular Medicine, Wellington School of Medicine and Health Sciences, Wellington, New Zealand.
Benjamin J ComptonThe Ferrier Research Institute, Victoria University of Wellington, Wellington, New Zealand.
Colin M HaymanThe Ferrier Research Institute, Victoria University of Wellington, Wellington, New Zealand.
Karen A JohnstonThe Ferrier Research Institute, Victoria University of Wellington, Wellington, New Zealand.ORCID 0000000151521410
Deborah A KnightMalaghan Institute of Medical Research, Wellington, New Zealand.
Olivier GasserMalaghan Institute of Medical Research, Wellington, New Zealand.
Hazel C PoyntzMalaghan Institute of Medical Research, Wellington, New Zealand.
Peter M FergusonCapital and Coast District Health Board, Wellington, New Zealand.
David S LarsenDepartment of Chemistry, University of Otago, Dunedin, New Zealand.
Franca RoncheseMalaghan Institute of Medical Research, Wellington, New Zealand.
Gavin F PainterThe Ferrier Research Institute, Victoria University of Wellington, Wellington, New Zealand.
Ian F Hermans1] Malaghan Institute of Medical Research, Wellington, New Zealand. [2] School of Biological Sciences, Victoria University of Wellington, Wellington, New Zealand.
Malaghan Institute of Medical Research · NZVictoria University of Wellington · NZCapital and Coast District Health Board · NZUniversity of Otago · NZ

Funding

PHS HHS HHSN272201300006C
6 · The paper itself

Abstract

Epitope-based peptide vaccines encompass minimal immunogenic regions of protein antigens to allow stimulation of precisely targeted adaptive immune responses. However, because efficacy is largely determined by the functional status of antigen-presenting cells (APCs) that acquire and present peptides to cells of the adaptive immune system, adjuvant compounds are needed to enhance immunogenicity. We present here a vaccine consisting of an allergen-derived peptide conjugated to a prodrug of the natural killer-like T (NKT) cell agonist α-galactosylceramide, which is highly effective in reducing inflammation in a mouse model of allergic airway inflammation. Unlike other peptide-adjuvant conjugates that directly activate APCs through pattern recognition pathways, this vaccine encourages third-party interactions with NKT cells to enhance APC function. Therapeutic efficacy was correlated with marked increases in the number and functional activity of allergen-specific cytotoxic T lymphocytes (CTLs), leading to suppression of immune infiltration into the lungs after allergen challenge in sensitized hosts.

Indexed as

Adjuvants, ImmunologicAllergensAnimalsAntigen-Presenting CellsAnti-Inflammatory AgentsDisease Models, AnimalFemaleGalactosylceramidesHypersensitivityImmunoglobulin EInflammationMaleMiceMice, Inbred C57BLMolecular ConformationNatural Killer T-CellsAdjuvants, ImmunologicAllergensalpha-galactosylceramideAnti-Inflammatory AgentsGalactosylceramidesImmunoglobulin EPeptidesProdrugsVaccines

Identifiers

PMID25282504
OpenAlexW2004276027

What OpenQuestion holds

Textmetadata
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.