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Updated: May 16, 2026

Lymphocyte Isolation from Human Skin for Phenotypic Analysis and Ex Vivo Cell Culture
Published on: April 8, 2016
Treatment-associated phenotype switching between psoriasis and atopic dermatitis
Tiago Torres1,2, Mario Valenti3,4, Anna Balato5
1Department of Dermatology, Centro Académico Clínico ICBAS/Santo António, Porto, Portugal.
Abstract:
Psoriasis and atopic dermatitis (AD) are traditionally viewed as distinct inflammatory skin diseases driven by type 17 and type 2 immune pathways, respectively. Increasing use of targeted therapies has revealed a treatment-associated phenotype switch between these conditions, the so-called 'flip-flop' phenomenon, characterized by sustained emergence of eczematous features in patients treated for psoriasis or psoriasiform disease in those treated for AD. Robust real-world data on this entity remain limited.
Objectives:
To characterize treatment-associated phenotype switching between psoriasis and AD in a large real-world cohort, focusing on clinical features, implicated therapies, management strategies and outcomes.
Methods:
We conducted a retrospective, multicentre, multinational observational study across 17 dermatology centres in six countries. Patients with psoriasis or AD who developed a clinician-defined, persistent phenotype switch temporally associated with systemic or biologic therapy and requiring treatment modification were included. Demographic, clinical, therapeutic and outcome data were collected and analysed descriptively.
Results:
A total of 148 patients were included: 101 (68.2%) developed eczematous features while treated for psoriasis (PsO → eczematous), and 47 (31.8%) developed psoriasiform disease while treated for AD (AD → psoriasiform). PsO → eczematous patients were older and had more cardiometabolic comorbidities, whereas atopic comorbidities were more frequent in the AD → psoriasiform group. PsO → eczematous switches occurred mainly under interleukin (IL)-17 and IL-23 inhibitors, while AD → psoriasiform switches occurred exclusively during biologic therapies targeting type 2 inflammation, predominantly dupilumab. Treatment was modified in all patients. Janus kinase (JAK) inhibitors were the most frequently used strategy in both switch directions, particularly in PsO → eczematous cases. Marked clinical improvement was observed across phenotypes following therapeutic adjustment.
Conclusions:
Treatment-associated phenotype switching between psoriasis and AD is a reproducible, bidirectional and clinically relevant real-world phenomenon reflecting immune plasticity rather than paradoxical disease induction. Recognition of this entity is essential to guide appropriate therapeutic adaptation, with JAK inhibitors emerging as a commonly effective management option.
Insights
Psoriasis and atopic dermatitis (AD) phenotype switching is a real-world phenomenon. Janus kinase (JAK) inhibitors effectively manage these treatment-associated immune changes, improving patient outcomes.
Area of Science:
- Dermatology and immunology
- Inflammatory skin diseases
- Therapeutic outcomes
Background:
- Psoriasis and atopic dermatitis (AD) are distinct inflammatory skin conditions.
- Targeted therapies reveal a 'flip-flop' phenomenon: eczematous changes in psoriasis patients or psoriasiform disease in AD patients.
- Limited real-world data exists on this treatment-associated phenotype switch.
Purpose of the Study:
- Characterize treatment-associated phenotype switching between psoriasis and AD.
- Analyze clinical features, therapies, management, and outcomes in a large real-world cohort.
Main Methods:
- Retrospective, multicentre, multinational observational study.
- Included patients with psoriasis or AD experiencing a persistent phenotype switch linked to systemic or biologic therapy.
- Collected and analyzed demographic, clinical, therapeutic, and outcome data.
Main Results:
- 148 patients included: 101 (PsO→eczematous) and 47 (AD→psoriasiform).
- PsO→eczematous switches linked to IL-17/IL-23 inhibitors; AD→psoriasiform switches linked to type 2 biologics (e.g., dupilumab).
- Janus kinase (JAK) inhibitors were the most common management strategy for both switch types, leading to marked clinical improvement.
Conclusions:
- Treatment-associated phenotype switching is a reproducible, bidirectional phenomenon reflecting immune plasticity.
- Recognizing this switch is crucial for appropriate therapeutic adaptation.
- JAK inhibitors show promise as an effective management option for these switches.
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