TNF-α signaling: TACE inhibition to put out the burning heart

More than 20 years ago, Seta and colleagues hypothesized that cytokines, which are activated by myocardial injury, significantly drive heart failure progression and would therefore be effective targets to treat cardiac dysfunction. Unfortunately, several clinical trials inhibiting key cytokines like...

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Hauptverfasser: Dittrich, Gesine M. (VerfasserIn) , Heineke, Jörg (VerfasserIn)
Dokumenttyp: Article (Journal)
Sprache:Englisch
Veröffentlicht: December 9, 2020
In: PLoS biology
Year: 2020, Jahrgang: 18, Heft: 12, Pages: 1-4
ISSN:1545-7885
DOI:10.1371/journal.pbio.3001037
Online-Zugang:Verlag, kostenfrei, Volltext: https://doi.org/10.1371/journal.pbio.3001037
Verlag, kostenfrei, Volltext: https://journals.plos.org/plosbiology/article?id=10.1371/journal.pbio.3001037
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Verfasserangaben:Gesine M. Dittrich, Joerg Heineke
Beschreibung
Zusammenfassung:More than 20 years ago, Seta and colleagues hypothesized that cytokines, which are activated by myocardial injury, significantly drive heart failure progression and would therefore be effective targets to treat cardiac dysfunction. Unfortunately, several clinical trials inhibiting key cytokines like tumor necrosis factor alpha (TNF-α) and interleukin 1 beta (Il-1β) turned out negative or even revealed adverse clinical effects. Providing a potential mechanistic explanation for the ineffectiveness of TNF-α blockade in heart failure, novel findings demonstrate that the membrane-bound precursor form of TNF-α, transmembrane TNF-α (tmTNF-α), mediates cardioprotective effects during pressure overload-induced cardiac remodeling. This study suggests that preventing tmTNF-α cleavage by targeting the TNF-α converting enzyme (TACE) rather than inhibiting TNF-α signaling altogether might be a valuable therapeutic approach.
Beschreibung:Gesehen am 16.07.2024
Beschreibung:Online Resource
ISSN:1545-7885
DOI:10.1371/journal.pbio.3001037