Evidence map›Paper›PMID 22308317›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2012

Cholera toxin activates nonconventional adjuvant pathways that induce protective CD8 T-cell responses after epicutaneous vaccination.

Irlanda Olvera-Gomez, Sara E Hamilton, Zhengguo Xiao, Carla P Guimaraes, Hidde L Ploegh, Kristin A Hogquist, Liangchun Wang, Stephen C Jameson

Open access · bronzeAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
2.4field-weighted citation impact, top 11% 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

14 citing papers in PubMed, 37 citations in OpenAlex.

  1. Article
  2. Article
  3. Bacteria-Inspired Nanomedicine.ACS applied bio materials · 2021
    Review
  4. Protective multi-epitope candidate vaccine for urinary tract infection.Biotechnology reports (Amsterdam, Netherlands) · 2020
    Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Antigen presentation by Langerhans cells.Current opinion in immunology · 2013
    Review
  13. Review
  14. 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

8 authors at 4 institutions in 1 country.

Irlanda Olvera-GomezCenter for Immunology, Department of Laboratory Medicine and Pathology, University of Minnesota Medical School, Minneapolis MN 55414, USA.
Sara E Hamilton
Zhengguo Xiao
Carla P Guimaraes
Hidde L Ploegh
Kristin A Hogquist
Liangchun Wang
Stephen C Jameson
University of Minnesota Medical Center · USMassachusetts Institute of Technology · USUniversity of Maryland, College Park · USWhitehead Institute for Biomedical Research · US

Funding

TRAINING GRANT IN MICROBIOLOGY/CANCER RESEARCHT32CA009138 · NCI · UNIVERSITY OF MINNESOTA TWIN CITIES · PI Scott M. Dehm · 1985 to 2026
$11.3M
Developing epicutaneous vaccine approaches for protective immunityU01AI070380 · NIAID · UNIVERSITY OF MINNESOTA · PI JAMESON, STEPHEN C · 2006 to 2010
$1.9M
NCI NIH HHS T32 CA009138NIAID NIH HHS U01 AI070380
6 · The paper itself

Abstract

The ability to induce humoral and cellular immunity via antigen delivery through the unbroken skin (epicutaneous immunization, EPI) has immediate relevance for vaccine development. However, it is unclear which adjuvants induce protective memory CD8 T-cell responses by this route, and the molecular and cellular requirements for priming through intact skin are not defined. We report that cholera toxin (CT) is superior to other adjuvants in its ability to prime memory CD8 T cells that control bacterial and viral challenges. Epicutaneous immunization with CT does not require engagement of classic toll-like receptor (TLR) and inflammasome pathways and, surprisingly, is independent of skin langerin-expressing cells (including Langerhans cells). However, CT adjuvanticity required type-I IFN sensitivity, participation of a Batf3-dependent dendritic cell (DC) population and engagement of CT with suitable gangliosides. Chemoenzymatic generation of CT-antigen fusion proteins led to efficient priming of the CD8 T-cell responses, paving the way for development of this immunization strategy as a therapeutic option.

Indexed as

VaccinationAdjuvants, ImmunologicAdministration, CutaneousAnimalsAntigensAntigens, SurfaceBasic-Leucine Zipper Transcription FactorsCD8-Positive T-LymphocytesCells, CulturedCholera ToxinG(M1) GangliosideImmunologic MemoryInterferon Type ILectins, C-TypeMannose-Binding LectinsMiceAdjuvants, ImmunologicAntigensAntigens, SurfaceBasic-Leucine Zipper Transcription FactorsCd207 protein, mouseCholera ToxinCPG-oligonucleotideG(M1) GangliosideInterferon Type ILectins, C-TypeMannose-Binding LectinsOligodeoxyribonucleotidesRepressor ProteinsSNFT protein, mouseToll-Like Receptors

Identifiers

PMID22308317
PMCPMC3277558
OpenAlexW2020059499

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.