Direkt zum Inhalt

Buchtler, Simone ; Frühauf, Antje ; Neumayer, Sophia ; Schmidbauer, Kathrin ; Talke, Yvonne ; Winter-Köhler, Frederike ; Balam, Saidou ; Landgraf, Karin ; Gebhard, Claudia ; Rehli, Michael ; Schlieckau, Florian Volker ; Beck, Maria ; Günther, Florian ; Fleck, Martin ; Renner, Kerstin ; Mack, Matthias

Fibrosis-memory is mediated by IL-3–producing T cells and drives progression of fibrosis

Buchtler, Simone, Frühauf, Antje, Neumayer, Sophia, Schmidbauer, Kathrin, Talke, Yvonne, Winter-Köhler, Frederike, Balam, Saidou , Landgraf, Karin, Gebhard, Claudia , Rehli, Michael , Schlieckau, Florian Volker, Beck, Maria, Günther, Florian, Fleck, Martin, Renner, Kerstin und Mack, Matthias (2026) Fibrosis-memory is mediated by IL-3–producing T cells and drives progression of fibrosis. Journal of Clinical Investigation 136 (6).

Veröffentlichungsdatum dieses Volltextes: 29 Apr 2026 12:22
Artikel
DOI zum Zitieren dieses Dokuments: 10.5283/epub.79363


Zusammenfassung

Repetitive injuries are an important trigger of progressive fibrosis. To study if repetitive injuries induce an accelerated profibrotic process, also called “fibrosis-memory,” we established an experimental system with two consecutive, clearly separated insults in a model of renal fibrosis with reversible and irreversible unilateral ureteral obstruction. We found that a preceding fibrotic event ...

Repetitive injuries are an important trigger of progressive fibrosis. To study if repetitive injuries induce an accelerated profibrotic process, also called “fibrosis-memory,” we established an experimental system with two consecutive, clearly
separated insults in a model of renal fibrosis with reversible and irreversible unilateral ureteral obstruction. We found that a preceding fibrotic event of one kidney markedly enhanced subsequent development of fibrosis in the contralateral kidney.
Aggravation of fibrosis during the second insult was dependent on memory CD4+ T cells. T cell depletion abrogated the fibrosis-memory effect, while adoptive transfer of memory T cells from fibrotic mice enhanced fibrosis in the recipients.
Moreover, IL-3 production by memory CD4+ T cells was essential for aggravation of fibrosis in memory situations. In patients with systemic sclerosis, IL-3 expression by T cells was markedly increased, especially after a long disease duration
accompanied by involvement of internal organs. In summary, our data identify IL-3–mediated fibrosis-memory as an important driver of progressive fibrosis.



Beteiligte Einrichtungen


Details

DokumentenartArtikel
Titel eines Journals oder einer ZeitschriftJournal of Clinical Investigation
Verlag:American Society for Clinical Investigation
Band:136
Nummer des Zeitschriftenheftes oder des Kapitels:6
Datum16 März 2026
InstitutionenMedizin > Abteilung für Nephrologie
Projekte
Gefördert von: Deutsche Forschungsgemeinschaft (DFG) (509149993)
Identifikationsnummer
WertTyp
10.1172/JCI192095DOI
Dewey-Dezimal-Klassifikation600 Technik, Medizin, angewandte Wissenschaften > 610 Medizin
StatusVeröffentlicht
BegutachtetJa, diese Version wurde begutachtet
An der Universität Regensburg entstandenJa
URN der UB Regensburgurn:nbn:de:bvb:355-epub-793639
Dokumenten-ID79363

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