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

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BORIS DOI
10.48620/84703
Publisher DOI
10.1038/s41467-024-54559-6
PubMed ID
39695162
Description
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.
Date of Publication
2024-12-18
Publication Type
Article
Subject(s)
600 - Technology::610 - Medicine & health
Language(s)
en
Contributor(s)
Seremet, Teofila
Di Domizio, Jeremy
Girardin, Antoine
Yatim, Ahmad
Jenelten, Raphael
Messina, Francesco
Saidoune, Fanny
Schlapbach, Christoph
Clinic of Dermatology
Bogiatzi, Sofia
Minisini, Frederic
Garzorz-Stark, Natalie
Leuenberger, Matthieu
Wüthrich, Héloise
Vernez, Maxime
Hohl, Daniel
Eyerich, Stefanie
Eyerich, Kilian
Guenova, Emmanuella
Paul, Carle
Gottardo, Raphael
Conrad, Curdin
Gilliet, Michel
Additional Credits
Clinic of Dermatology
Series
Nature Communications
Publisher
Nature Research
ISSN
2041-1723
Access(Rights)
open.access
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