Evidence map›Paper›PMID 37727790›Full record

ArticleFrontiers in immunology2023

Optimized dithranol-imiquimod-based transcutaneous immunization enables tumor rejection.

Ann-Kathrin Hartmann, Joschka Bartneck, Jonas Pielenhofer, Sophie Luise Meiser, Danielle Arnold-Schild, Matthias Klein, Michael Stassen, Hansjörg Schild, Sabine Muth, Hans Christian Probst and 3 more

Abstract read
In one paragraph

Article in Frontiers in immunology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Review
  2. Review
  3. Article
  4. Tumor-infiltrating CCR2Frontiers in immunology · 2023
    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

13 authors.

Ann-Kathrin HartmannIIIrd Department of Medicine - Hematology and Oncology, University Medical Center of the Johannes Gutenberg-University, Mainz, Germany.
Joschka BartneckIIIrd Department of Medicine - Hematology and Oncology, University Medical Center of the Johannes Gutenberg-University, Mainz, Germany.
Jonas PielenhoferBiopharmaceutics and Pharmaceutical Technology, Institute of Pharmacy and Biochemistry, Johannes Gutenberg-University, Mainz, Germany.
Sophie Luise MeiserBiopharmaceutics and Pharmaceutical Technology, Institute of Pharmacy and Biochemistry, Johannes Gutenberg-University, Mainz, Germany.
Danielle Arnold-SchildInstitute of Immunology, University Medical Center of the Johannes Gutenberg-University, Mainz, Germany.
Matthias KleinInstitute of Immunology, University Medical Center of the Johannes Gutenberg-University, Mainz, Germany.
Michael StassenInstitute of Immunology, University Medical Center of the Johannes Gutenberg-University, Mainz, Germany.
Hansjörg SchildInstitute of Immunology, University Medical Center of the Johannes Gutenberg-University, Mainz, Germany.
Sabine MuthInstitute of Immunology, University Medical Center of the Johannes Gutenberg-University, Mainz, Germany.
Hans Christian ProbstInstitute of Immunology, University Medical Center of the Johannes Gutenberg-University, Mainz, Germany.
Peter LangguthBiopharmaceutics and Pharmaceutical Technology, Institute of Pharmacy and Biochemistry, Johannes Gutenberg-University, Mainz, Germany.
Stephan GrabbeResearch Center for Immunotherapy (FZI), University Medical Center of the Johannes Gutenberg-University, Mainz, Germany.
Markus P RadsakIIIrd Department of Medicine - Hematology and Oncology, University Medical Center of the Johannes Gutenberg-University, Mainz, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Transcutaneous immunization (TCI) is a non-invasive vaccination method promoting strong cellular immune responses, crucial for the immunological rejection of cancer. Previously, we reported on the combined application of the TLR7 agonist imiquimod (IMQ) together with the anti-psoriatic drug dithranol as novel TCI platform DIVA (dithranol/IMQ based vaccination). In extension of this work, we further optimized DIVA in terms of drug dose, application pattern and established a new IMQ formulation. Methods: C57BL/6 mice were treated on the ear skin with dithranol and IMQ-containing ointments together with ovalbumin-derived peptides. T cell responses were determined by flow cytometry and IFN-ɤ ELISpot assay, local skin inflammation was characterized by ear swelling. Results: Applying the adjuvants on separate skin sites, a reduced number of specific CD8 Discussion: Taken together, the described optimized transcutaneous vaccination method leads to the generation of a strong cellular immune response enabling the effective control of tumor growth and has the potential for clinical development as a novel non-invasive vaccination method for peptide-based cancer vaccines in humans.

Indexed as

DermatitisNeoplasmsAdjuvants, ImmunologicAnimalsAnthralinCD8-Positive T-LymphocytesHumansImiquimodImmunizationMiceMice, Inbred C57BLVaccinationAdjuvants, ImmunologicAnthralinImiquimodcytotoxic T lymphocytes (CTL)dithranol (anthralin)imiquimod (IMQ)trancutaneous immunizationtumor rejection

Identifiers

PMID37727790
PMCPMC10505723

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Registered trials

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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.