Evidence map›Paper›PMID 40790057›Full record

ArticleScientific reports2025

Sustained learned immunosuppression could not prevent local allergic ear swelling in a rat model of contact hypersensitivity.

Yasmin Salem, Stephan Leisengang, Marie Jakobs, Kirsten Dombrowski, Julia Bihorac, Laura Heiss-Lückemann, Sebastian Wenzlaff, Lisa Trautmann, Tim Hagernacker, Manfred Schedlowski and 1 more

Abstract read
In one paragraph

Article in Scientific reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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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

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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

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0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

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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

11 authors.

Yasmin SalemInstitute of Medical Psychology and Behavioral Immunobiology, Center for Translational Neuro- Behavioral Sciences (C-TNBS), University Hospital Essen, Essen, Germany.
Stephan LeisengangInstitute of Medical Psychology and Behavioral Immunobiology, Center for Translational Neuro- Behavioral Sciences (C-TNBS), University Hospital Essen, Essen, Germany.
Marie JakobsInstitute of Medical Psychology and Behavioral Immunobiology, Center for Translational Neuro- Behavioral Sciences (C-TNBS), University Hospital Essen, Essen, Germany.
Kirsten DombrowskiInstitute of Medical Psychology and Behavioral Immunobiology, Center for Translational Neuro- Behavioral Sciences (C-TNBS), University Hospital Essen, Essen, Germany.
Julia BihoracInstitute of Medical Psychology and Behavioral Immunobiology, Center for Translational Neuro- Behavioral Sciences (C-TNBS), University Hospital Essen, Essen, Germany.
Laura Heiss-LückemannInstitute of Medical Psychology and Behavioral Immunobiology, Center for Translational Neuro- Behavioral Sciences (C-TNBS), University Hospital Essen, Essen, Germany.
Sebastian WenzlaffInstitute of Medical Psychology and Behavioral Immunobiology, Center for Translational Neuro- Behavioral Sciences (C-TNBS), University Hospital Essen, Essen, Germany.
Lisa TrautmannInstitute of Medical Psychology and Behavioral Immunobiology, Center for Translational Neuro- Behavioral Sciences (C-TNBS), University Hospital Essen, Essen, Germany.
Tim HagernackerDepartment of Neurology, Center for Translational Neuro-Behavioral Sciences (C- TNBS), University Hospital Essen, Essen, Germany.
Manfred SchedlowskiInstitute of Medical Psychology and Behavioral Immunobiology, Center for Translational Neuro- Behavioral Sciences (C-TNBS), University Hospital Essen, Essen, Germany.
Martin HadamitzkyInstitute of Medical Psychology and Behavioral Immunobiology, Center for Translational Neuro- Behavioral Sciences (C-TNBS), University Hospital Essen, Essen, Germany. martin.hadamitzky@uk-essen.de.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Taste-immune associative learning has been shown to mimic immunopharmacological responses. Conditioned pharmacological effects may therefore be considered as controlled drug dose reduction strategy to maintain treatment efficacy. Against this background, the present study applied an established taste-immune associative learning protocol to a rat model of DNFB-induced contact hypersensitivity. After repeated pairings of a saccharin taste (conditioned stimulus, CS) with injections of the immunosuppressant cyclosporine A (CsA, unconditioned stimulus, UCS), animals were sensitized with the hapten. Retrieval started by presenting the CS together with sub-effective doses of CsA. This procedure preserved a conditioned suppression of splenic cytokine production. Compared to full dose treated animals, conditioned effects were neither observed in draining lymph nodes nor did it prevent ear swelling. These findings suggest that active sensitization might have masked a potential conditioned reduction of local allergic reactions. Additionally, symptoms such as itch may be more suited as readout parameter since it better reflects patients' disease burden. The present study reaffirms that learned immunopharmacological effects can be preserved using a memory-updating approach. It also emphasizes the need to further explore the usability of associative learning protocols in clinical contexts in order to address disease-specific symptoms more effectively.

Indexed as

Dermatitis, Allergic ContactImmunosuppression TherapyImmunosuppressive AgentsAnimalsCyclosporineCytokinesDinitrofluorobenzeneDisease Models, AnimalEarMaleRatsSpleenTasteCyclosporineCytokinesDinitrofluorobenzeneImmunosuppressive AgentsAssociative learningContact hypersensitivityCyclosporine ADose reductionMemory-updating

Identifiers

PMID40790057
PMCPMC12340026

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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.