Immune modules to guide diagnosis and personalized treatment of inflammatory skin diseases

Previous advances have identified immune pathways associated with inflammatory skin diseases, leading to the development of targeted therapies. However, there is a lack of molecular approaches that delineate these pathways at the individual patient level for personalized diagnostic and therapeutic guidance. Here, we conduct a cross-comparison of expression profiles from multiple inflammatory skin diseases to identify gene modules defining relevant immune pathways. Seven modules are identified, representing key immune pathways: Th17, Th2, Th1, Type I IFNs, neutrophilic, macrophagic, and eosinophilic. These modules allow the development of a molecular map with high diagnostic efficacy for inflammatory skin diseases and clinico-pathologically undetermined cases. Aligning dominant modules with treatment targets offers a rational framework for treatment selection, improving response rates in both treatment-naïve patients and non-responders to targeted therapies. Overall, our approach offers precision medicine for inflammatory skin diseases, utilizing transcriptional modules to support diagnosis and guide personalized treatment selection.

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Institutions

Publication Details

Journal
Nature Communications
Published
2024-12-18
DOI
https://doi.org/10.1038/s41467-024-54559-6
Citations
34
Primary Topic
Dermatology and Skin Diseases
Type
article
Field-Weighted Citation Impact
18.18

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article

Immune modules to guide diagnosis and personalized treatment of inflammatory skin diseases

Raphaël Gottardo, Raphael Jenelten, Héloïse Wüthrich, Christoph Schlapbach et al.
34 citations
Nature Communications
Dermatology and Skin Diseases
18.18
article

Immune modules to guide diagnosis and personalized treatment of inflammatory skin diseases

Raphaël Gottardo, Raphael Jenelten, Héloïse Wüthrich, Christoph Schlapbach, Natalie Garzorz‐Stark, Frédéric Minisini, Ahmad Yatim, Antoine Girardin, Curdin Conrad, Teofila Seremet, Michel Gilliet, Stefanie Eyerich, Maxime Vernez, Jérémy Di Domizio, Emmanuella Guenova, Mathieu Leuenberger, C. Paul, Daniel Hohl, Kilian Eyerich, Fanny Saidoune, Sofia Bogiatzi, Francesco Messina
article en
34 citations

Abstract

Previous advances have identified immune pathways associated with inflammatory skin diseases, leading to the development of targeted therapies. However, there is a lack of molecular approaches that delineate these pathways at the individual patient level for personalized diagnostic and therapeutic guidance. Here, we conduct a cross-comparison of expression profiles from multiple inflammatory skin diseases to identify gene modules defining relevant immune pathways. Seven modules are identified, representing key immune pathways: Th17, Th2, Th1, Type I IFNs, neutrophilic, macrophagic, and eosinophilic. These modules allow the development of a molecular map with high diagnostic efficacy for inflammatory skin diseases and clinico-pathologically undetermined cases. Aligning dominant modules with treatment targets offers a rational framework for treatment selection, improving response rates in both treatment-naïve patients and non-responders to targeted therapies. Overall, our approach offers precision medicine for inflammatory skin diseases, utilizing transcriptional modules to support diagnosis and guide personalized treatment selection.

Nature CommunicationsVol. 15(1)
University of Bern (CH), University of Freiburg (DE), University Hospital of Bern (CH), University Medical Center Freiburg (DE), Centre Hospitalier Universitaire Vaudois (CH), Hôpital Orthopédique de la Suisse Romande (CH), University of Lausanne (CH)
National Science Foundation, Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung, Fondation Leenaards
Good health and well-being
Openalex Percentile: Top 0%
Dermatology and Skin Diseases
18.18
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