Transition From Psoriasis to Psoriatic Arthritis is Characterized by Distinct Alterations in Peripheral Blood Tc17, Th17, and <scp>CD4</scp> <sup>+</sup> Effector Memory Cells

Transition from psoriasis to psoriatic arthritis was associated with distinct alterations of the peripheral blood T cell compartment, with Tc17 cells exhibiting the greatest discriminatory power. These findings provide insight into pathomechanisms driving disease progression during transition from psoriasis to psoriatic arthritis and identify Tc17 cells as the foremost novel potential therapeutic target for the prevention of transition.

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Publication Details

Journal
Arthritis & Rheumatology
Published
2025-09-16
DOI
https://doi.org/10.1002/art.43396
Citations
1
Primary Topic
Autoimmune and Inflammatory Disorders Research
Type
article
Field-Weighted Citation Impact
1.77

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article

Transition From Psoriasis to Psoriatic Arthritis is Characterized by Distinct Alterations in Peripheral Blood Tc17, Th17, and CD4 + Effector Memory Cells

Hanna Graßhoff, Sabrina Arnold, Henry Nording, Linh Ha‐Wissel et al.
1 citations
Arthritis & Rheumatology
Autoimmune and Inflammatory Disorders Research
1.77
article

Transition From Psoriasis to Psoriatic Arthritis is Characterized by Distinct Alterations in Peripheral Blood Tc17, Th17, and CD4 + Effector Memory Cells

Hanna Graßhoff, Sabrina Arnold, Henry Nording, Linh Ha‐Wissel, Gabriela Riemekasten, Sara Comdühr, Henner Zirpel, Peter Lamprecht, Jens Y. Humrich, El‐Baraa Adjailia, Ingo Eitel, Sebastian Klapa, Oliver Josef Müller, Habip Gedık, Konstantinos Fourlakis, Philine Letz, Diamant Thaçi, Jacob von Esebeck, Miriam Prohaczka, Elisabeth Spallek
article en
1 citations

Abstract

Transition from psoriasis to psoriatic arthritis was associated with distinct alterations of the peripheral blood T cell compartment, with Tc17 cells exhibiting the greatest discriminatory power. These findings provide insight into pathomechanisms driving disease progression during transition from psoriasis to psoriatic arthritis and identify Tc17 cells as the foremost novel potential therapeutic target for the prevention of transition.

Arthritis & RheumatologyVol. 78(2)
Universität Hamburg (DE), Hochschule für Angewandte Wissenschaften Kiel (DE), Christian-Albrechts-Universität zu Kiel (DE), University Medical Center Hamburg-Eppendorf (DE), German Centre for Cardiovascular Research (DE), Clinical Research Center Kiel (DE), University of Lübeck (DE)
Amgen, Bristol-Myers Squibb, Eli Lilly and Company, Pfizer, AstraZeneca, Sanofi, Regeneron Pharmaceuticals, Celltrion, European Commission, Deutsche Forschungsgemeinschaft, Bundesministerium für Bildung und Forschung, Daiichi-Sankyo, Bundesministerium der Verteidigung, Vifor Pharma, Galderma, LEO Pharma, Chugai Pharmaceutical, HORIZON EUROPE Framework Programme, UCB Pharma, Cilag
Openalex Percentile: Top 13%
Autoimmune and Inflammatory Disorders Research
1.77
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