Single cell mapping identifies a distinct platelet-phenotype in psoriatic type III inflammation

The understanding of platelet biology is expanding beyond their well-established role in thrombosis and hemostasis to encompass their functions in inflammation. To gain insights into the phenotype and possible platelet-subgroups in the context of type III inflammation, high-parametric single cell spectral flow cytometry was applied to a prospectively followed cohort of psoriasis patients undergoing systemic therapy. By focusing on the activation profile of platelets and their interaction with immune cells, we identify cell-surface proteins CD32<sup>+</sup>CD154<sup>+</sup> and TLR2<sup>+</sup>TLR4<sup>+</sup>, distinguishing unique platelet subsets in psoriasis patients. These subsets demonstrate regression over the course of systemic therapy. Notably, these platelet phenotypes and frequencies differ from those of healthy controls, and patients with atopic dermatitis (AD), a type II inflammation-driven disease. Our data highlight a specific platelet phenotype responding acutely to the respective inflammatory context. This finding warrants further investigation into platelets as a diagnostic tool in inflammatory conditions, necessitating future insight into the function of these subsets across disease etiologies.

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Publication Details

Journal
Nature Communications
Published
2025-12-05
DOI
https://doi.org/10.1038/s41467-025-65894-7
Citations
1
Primary Topic
Psoriasis: Treatment and Pathogenesis
Type
article
Field-Weighted Citation Impact
0.80
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article

Single cell mapping identifies a distinct platelet-phenotype in psoriatic type III inflammation

Alexander Enk, Francesca Barletta, Sven Nahnsen, Tabea Bieler et al.
1 citations
Nature Communications
Psoriasis: Treatment and Pathogenesis
0.80
article

Single cell mapping identifies a distinct platelet-phenotype in psoriatic type III inflammation

Alexander Enk, Francesca Barletta, Sven Nahnsen, Tabea Bieler, Mathias Heikenwälder, Dominic Helm, Stefan Czemmel, Sandra Prokosch, Katharina Susanne Kommoss, Ulrike Rothermel, Burkhard Becher, Ekaterina Friebel, Yulin Wu, Pierluigi Ramadori, Lukas Rindlisbacher, Knut Schäkel, Sinduya Krishnarajah, Florian L. Müller, Philipp Häne, Martin Schneider, Shing Kam
article en
1 citations

Abstract

The understanding of platelet biology is expanding beyond their well-established role in thrombosis and hemostasis to encompass their functions in inflammation. To gain insights into the phenotype and possible platelet-subgroups in the context of type III inflammation, high-parametric single cell spectral flow cytometry was applied to a prospectively followed cohort of psoriasis patients undergoing systemic therapy. By focusing on the activation profile of platelets and their interaction with immune cells, we identify cell-surface proteins CD32<sup>+</sup>CD154<sup>+</sup> and TLR2<sup>+</sup>TLR4<sup>+</sup>, distinguishing unique platelet subsets in psoriasis patients. These subsets demonstrate regression over the course of systemic therapy. Notably, these platelet phenotypes and frequencies differ from those of healthy controls, and patients with atopic dermatitis (AD), a type II inflammation-driven disease. Our data highlight a specific platelet phenotype responding acutely to the respective inflammatory context. This finding warrants further investigation into platelets as a diagnostic tool in inflammatory conditions, necessitating future insight into the function of these subsets across disease etiologies.

Nature CommunicationsVol. 16(1)
Roche (Switzerland) (CH), German Cancer Research Center (DE), University of Zurich (CH), Heidelberg University (DE), University Hospital Heidelberg (DE), Bernstein Center for Computational Neuroscience Tübingen (DE), Charité - Universitätsmedizin Berlin (DE), University of Tübingen (DE)
Openalex Percentile: Top 21%
Psoriasis: Treatment and Pathogenesis
0.80
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