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

Artikel

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).

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
VerlagAmerican Society for Clinical Investigation
Open Access ArtGold (mit APC - bezahlt UR)
Band136
Nummer des Zeitschriftenheftes oder des Kapitels6
Datum16 März 2026
Veröffentlichungsdatum29 Apr 2026 12:22
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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