Evidence map›Paper›PMID 41732608›Full record

ArticleCureus2026

Targeting the IL-36 Pathway: Spesolimab as a Therapeutic for Acute Flares of Pustular Psoriasis.

Esther Nwozo, Devon Cross, David Smith

Abstract readCase Reports
In one paragraph

Article in Cureus, 2026. 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

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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

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

3 authors.

Esther NwozoSchool of Medicine, Lewis Katz School of Medicine at Temple University, Philadelphia, USA.
Devon CrossDepartment of Dermatology, St. Luke's University Health Network, Easton, USA.
David SmithDepartment of Dermatology, St. Luke's University Health Network, Easton, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Generalized pustular psoriasis (GPP) is a rare and severe subtype of psoriasis characterized by widespread sterile pustules, erythema, and systemic inflammation. The condition is mediated by dysregulation of the IL-36 signaling pathway, which promotes excessive cytokine release and neutrophilic infiltration. Traditional therapies, including corticosteroids and immunosuppressive agents such as cyclosporine or methotrexate, often fail to achieve rapid or sustained disease control. Spesolimab, a monoclonal antibody that inhibits the IL-36 receptor, represents a novel targeted therapy approved for the treatment of acute GPP flares in adults. We describe a 56-year-old woman with no significant past medical history who presented with diffuse erythematous and scaly plaques involving the trunk, face, groin, and extremities. Initial biopsy findings were consistent with an eczematous dermatitis, and her eruption temporarily resolved with topical corticosteroids and a prednisone taper. Five months later, she developed diffuse pustules covering 80% of her body surface area (BSA), accompanied by fever, chills, and joint pain. A repeat biopsy demonstrated subcorneal neutrophilic pustules consistent with pustular psoriasis. She was treated with cyclosporine, resulting in partial improvement to 30% body surface area involvement. The patient subsequently received a 900 mg intravenous dose of spesolimab, which produced marked improvement within two weeks, leaving less than 5% body surface area involvement. Ongoing therapy with cyclosporine and planned monthly spesolimab infusions maintained disease remission. This case highlights the rapid efficacy and sustained control achieved with spesolimab in an acute flare of GPP refractory to conventional therapy. The results underscore the importance of IL-36 inhibition in targeting the underlying inflammatory pathway and suggest that early initiation of spesolimab may improve outcomes in patients with moderate-to-severe disease.

Indexed as

biologic therapygeneralized pustular psoriasisil-36 pathwayimmunodermatologymonoclonal antibodypsoriasisspesolimab

Identifiers

PMID41732608
PMCPMC12925328

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