Evidence map›Paper›PMID 25121970›Full record

ArticlePloS one2014

Efficiency of dendritic cell vaccination against B16 melanoma depends on the immunization route.

Fanny Edele, Jan C Dudda, Eva Bachtanian, Thilo Jakob, Hanspeter Pircher, Stefan F Martin

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.2field-weighted citation impact, top 22% 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

11 citing papers in PubMed, 21 citations in OpenAlex.

  1. Article
  2. Microneedle-Mediated Cell Therapy.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2024
    Review
  3. Review
  4. Cryomicroneedles for transdermal cell delivery.Nature biomedical engineering · 2021
    Article
  5. Article
  6. Synthetic immune niches for cancer immunotherapy.Nature reviews. Immunology · 2018
    Review
  7. Article
  8. Article
  9. Review
  10. Article
  11. 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

6 authors at 1 institution in 1 country.

Fanny EdeleAllergy Research Group, Department of Dermatology, Medical Center - University of Freiburg, Freiburg, Germany.
Jan C DuddaAllergy Research Group, Department of Dermatology, Medical Center - University of Freiburg, Freiburg, Germany.
Eva BachtanianAllergy Research Group, Department of Dermatology, Medical Center - University of Freiburg, Freiburg, Germany.
Thilo JakobAllergy Research Group, Department of Dermatology, Medical Center - University of Freiburg, Freiburg, Germany.
Hanspeter PircherInstitute for Medical Microbiology and Hygiene, Medical Center - University of Freiburg, Freiburg, Germany.
Stefan F MartinAllergy Research Group, Department of Dermatology, Medical Center - University of Freiburg, Freiburg, Germany.
University of Freiburg · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Dendritic cells (DC) presenting tumor antigens are crucial to induce potent T cell-mediated anti-tumor immune responses. Therefore DC-based cancer vaccines have been established for therapy, however clinical outcomes are often poor and need improvement. Using a mouse model of B16 melanoma, we found that the route of preventive DC vaccination critically determined tumor control. While repeated DC vaccination did not show an impact of the route of DC application on the prevention of tumor growth, a single DC vaccination revealed that both the imprinting of skin homing receptors and an enhanced proliferation state of effector T cells was seen only upon intracutaneous but not intravenous or intraperitoneal immunization. Tumor growth was prevented only by intracutaneous DC vaccination. Our results indicate that under suboptimal conditions the route of DC vaccination crucially determines the efficiency of tumor defense. DC-based strategies for immunotherapy of cancer should take into account the immunization route in order to optimize tissue targeting of tumor antigen specific T cells.

Indexed as

ImmunizationAdoptive TransferAnimalsAntigens, ViralCancer VaccinesCell Line, TumorDendritic CellsDisease Models, AnimalGene ExpressionGlycoproteinsImmunotherapyLymphocyte ActivationMelanoma, ExperimentalMiceMice, TransgenicPeptide FragmentsAntigens, ViralCancer Vaccinesglycoprotein peptide 33-41, Lymphocytic choriomeningitis virusGlycoproteinsPeptide FragmentsReceptors, Antigen, T-CellReceptors, Lymphocyte HomingViral Proteins

Identifiers

PMID25121970
PMCPMC4133283
OpenAlexW2088645151

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.