Collagen remodeling is elevated in fibrotic hypersensitivity…

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  • DOI 10.1186/s12890-026-04676-3
  • OpenAlex ID W7206172956
  • Type Article
  • Language EN
  • Published 03 Sep 2026
  • Source BMC Pulmonary Medicine
  • Publisher BioMed Central
  • Countries 1
  • Institutions 6
  • Added 03 Sep 2026
  • Updated 08 Oct 2026
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Collagen remodeling is elevated in fibrotic hypersensitivity pneumonitis and may distinguish it from idiopathic pulmonary fibrosis

Article 2026 EN Gold

Idiopathic pulmonary fibrosis (IPF) and fibrotic hypersensitivity pneumonitis (fHP) are two common causes of pulmonary fibrosis. Unlike IPF, fHP is caused by a persistent immune response to an antigen. Misclassification of fHP and IPF can lead to significant delays in antifibrotic treatment, particularly in cases where the eliciting antigen cannot be identified and removed. Extracellular matrix (E…

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UN Sustainable Development Goals
1 SDGs
Authors & Affiliations
10 authors
#AuthorInstitutionsORCID
1 Georgia Christoforidou University of Copenhagen (DK) Nordic Bioscience (Denmark) (DK)
2 Filipa Bica Simões Nordic Bioscience (Denmark) (DK)
3 Sandra Duval Dræby Herlev Hospital (DK) Gentofte Hospital (DK) —
4 Sissel Brix Kronborg-White Aarhus University Hospital (DK)
5 Nils Hoyer Herlev Hospital (DK) Gentofte Hospital (DK)
6 M.A. Karsdal Nordic Bioscience (Denmark) (DK)
7 Diana Julie Leeming Nordic Bioscience (Denmark) (DK)
8 Elisabeth M. Bendstrup Aarhus University (DK) Aarhus University Hospital (DK)
9 Saher Burhan Shaker Herlev Hospital (DK) Gentofte Hospital (DK) —
10 Jannie Marie Bülow Sand Corresponding Nordic Bioscience (Denmark) (DK)

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