Nature Communications (Dec 2024)

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

  • Teofila Seremet,
  • Jeremy Di Domizio,
  • Antoine Girardin,
  • Ahmad Yatim,
  • Raphael Jenelten,
  • Francesco Messina,
  • Fanny Saidoune,
  • Christoph Schlapbach,
  • Sofia Bogiatzi,
  • Frederic Minisini,
  • Natalie Garzorz-Stark,
  • Matthieu Leuenberger,
  • Héloise Wüthrich,
  • Maxime Vernez,
  • Daniel Hohl,
  • Stefanie Eyerich,
  • Kilian Eyerich,
  • Emmanuella Guenova,
  • Carle Paul,
  • Raphael Gottardo,
  • Curdin Conrad,
  • Michel Gilliet

DOI
https://doi.org/10.1038/s41467-024-54559-6
Journal volume & issue
Vol. 15, no. 1
pp. 1 – 12

Abstract

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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.