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Leiber, L.M.* ; Christian, L.* ; Neubert, L.* ; Ruwisch, J.* ; Yilmaz, H.* ; Plucinski, E.K.J.* ; Langer, L.T.* ; Kamp, J.C.* ; Greer, M.* ; Haermeyer, B.* ; Mark, K.* ; Werlein, C.* ; Justet, A.* ; Bergmann, A.* ; Beeckmans, H.* ; Ballmaier, M.* ; Salman, J.* ; Vos, R.* ; Knudsen, L.* ; Martin, U.* ; Vanaudenaerde, B.* ; Yildirim, A.Ö. ; Hohlfeld, J.M.* ; Ius, F.* ; Laenger, F.* ; Welte, T.* ; Falk, C.* ; Kaminski, N.* ; Jonigk, D.* ; Gottlieb, J.* ; Schupp, J.C.*

Aberrant and ectopic cell populations in restrictive allograft syndrome after lung transplantation.

Eur. Respir. J.:2500537 (2026)
Postprint DOI PMC
Open Access Green
RATIONALE: Restrictive allograft syndrome (RAS) is a major cause of mortality following lung transplantation due to progressive fibrosis of the lung allograft with no therapeutic options. Knowledge of the cellular and molecular mechanisms driving fibrosis in RAS remains limited. OBJECTIVE: To characterize the cellular and molecular changes in human RAS lungs through single-cell transcriptomic profiling. METHODS: Single-nucleus RNA-sequencing (snRNA-seq) was performed in peripheral lung tissues from 15 RAS patients undergoing lung re-transplantation, and from 9 healthy control lungs. Findings were validated and extended using histologic techniques including immunofluorescence, RNA in situ hybridization, Elastica-van-Gieson immunohistochemistry, quantitative histological analyses, and micro-CT scans. MEASUREMENTS AND MAIN RESULTS: snRNA-seq analysis of RAS lungs revealed previously undescribed aberrant basaloid cells, ectopic COL15A1+ peribronchial vascular endothelial cells (pVECs), and CTHRC1+ fibrotic fibroblasts. Histologic stains disclosed distinctive distribution patterns: aberrant basaloid cells, primarily localized at the fibrotic edge, together with juxtaposed CTHRC1+ fibrotic fibroblasts and ectopic COL15A1+ pVECs form the fibrotic niche of alveolar fibroelastosis (AFE). PRX+ alveolar microvasculature is partially lost in AFE areas. Micro-CT scans revealed changes from pulmonary to systemic perfusion, facilitated by COL15A1+ pVECs. Last, our data reveals potential therapeutic targets in RAS, including integrin αvβ6, activator of TGFβ. CONCLUSION: Considering the multifaceted differences of RAS and idiopathic pulmonary fibrosis, we revealed a surprising general principle of an entity-spanning composition of the fibrotic niche by aberrant basaloid cells localized at the fibrotic edge, ectopic COL15A1+ pVECs and CTHRC1+ fibrotic fibroblasts. This suggests a flexible but cellular pathogenesis-guided transferability of potential therapeutic approaches between progressive fibrotic lung diseases.
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Publikationstyp Artikel: Journalartikel
Dokumenttyp Wissenschaftlicher Artikel
Schlagwörter Fibrosis ; Lung Transplantation ; Lung ; Transplantation ; Extracellular Matrix ; Idiopathic Pulmonary Fibrosis ; Pulmonary Fibrosis ; Alveolar Wall
ISSN (print) / ISBN 0903-1936
e-ISSN 1399-3003
Zeitschrift European Respiratory Journal
Quellenangaben Band: , Heft: , Seiten: , Artikelnummer: 2500537 Supplement: ,
Verlag European Respiratory Society
Verlagsort Sheffield
Begutachtungsstatus Peer reviewed
Institut(e) Institute of Lung Health and Immunity (LHI)