Evidence map›Paper›PMID 41438421›Full record

ArticlePsoriasis (Auckland, N.Z.)2025

Antibodies Targeting Gasdermin E as a Potential Therapeutic Option for Psoriasis - A Pilot Study on a Mouse Model.

Julia Nowowiejska-Purpurowicz, Justyna M Hermanowicz, Dariusz Pawlak, Iwona Flisiak, Tomasz Lipinski

Abstract read
In one paragraph

Article in Psoriasis (Auckland, N.Z.), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

5 authors.

Julia Nowowiejska-PurpurowiczDepartment of Dermatology and Venereology, Medical University of Bialystok, Bialystok, 15-540, Poland.ORCID 0000-0002-6870-1167
Justyna M HermanowiczDepartment of Pharmacodynamics, Medical University of Bialystok, Bialystok, 15-222, Poland.
Dariusz PawlakDepartment of Pharmacodynamics, Medical University of Bialystok, Bialystok, 15-222, Poland.ORCID 0000-0002-3751-0608
Iwona Flisiak *Department of Dermatology and Venereology, Medical University of Bialystok, Bialystok, 15-540, Poland.
Tomasz Lipinski *Lukasiewicz Research Network - PORT Polish Center for Technology Development, Wrocław, 54-066, Poland.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Psoriasis is a frequent and complex dermatosis of uncertain origin. A few years ago, a family of gasdermin proteins was implicated in psoriasis pathogenesis. Although the number of therapeutic options for psoriasis is growing, considering the burden of the disease, treatment personalization, and the possibility of side effects or loss of the drug's efficacy, it is important to seek new therapeutic targets. Objective: The aim of this study was to assess the efficacy of antibodies against gasdermin E (GSDME) in the treatment of psoriatic lesions. Methods: The study involved 30 male BALB/c mice, 8 weeks old. 5% imiquimod cream was applied topically on the skin to induce psoriatic lesions. The next day after the psoriatic lesions appeared, the antibodies were administered. Mice from the study group received the rabbit polyclonal anti-GSDME antibody intravenously or intraperitoneally. The control group was administered sterile 0.9% saline solution. Results: The injection of anti-GSDME antibodies to mice with imiquimod-induced psoriasis resulted in the resolution of skin lesions, whereas the injection of saline to the control group did not result in significant changes. Conclusion: Antibodies targeting GSDME seem to be promising therapeutic agents in psoriasis; however, their utility has to be confirmed in future studies.

Indexed as

antibodygasdermingasdermin EGSDMEmouse modelpsoriasis

Identifiers

PMID41438421
PMCPMC12722015

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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.