Co-modulation of TNFR1 and TNFR2 in an animal model of multiple sclerosis

Tumour necrosis factor (TNF) is a pleiotropic cytokine and master regulator of the immune system. It acts through two receptors resulting in often opposing biological effects, which may explain the lack of therapeutic potential obtained so far in multiple sclerosis (MS) with non-receptor-specific an...

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Hauptverfasser: Fiedler, Timon (VerfasserIn) , Fairless, Richard (VerfasserIn) , Pichi, Kira (VerfasserIn) , Fischer, Roman (VerfasserIn) , Richter, Fabian (VerfasserIn) , Kontermann, Roland (VerfasserIn) , Pfizenmaier, Klaus (VerfasserIn) , Diem, Ricarda (VerfasserIn) , Williams-Fairless, Sarah K. (VerfasserIn)
Dokumenttyp: Article (Journal)
Sprache:Englisch
Veröffentlicht: 30 April 2023
In: Journal of neuroinflammation
Year: 2023, Jahrgang: 20, Pages: 1-13
ISSN:1742-2094
DOI:10.1186/s12974-023-02784-z
Online-Zugang:Verlag, kostenfrei, Volltext: https://doi.org/10.1186/s12974-023-02784-z
Verlag, kostenfrei, Volltext: https://jneuroinflammation.biomedcentral.com/articles/10.1186/s12974-023-02784-z
Volltext
Verfasserangaben:Timon Fiedler, Richard Fairless, Kira Pichi, Roman Fischer, Fabian Richter, Roland E. Kontermann, Klaus Pfizenmaier, Ricarda Diem and Sarah K. Williams
Beschreibung
Zusammenfassung:Tumour necrosis factor (TNF) is a pleiotropic cytokine and master regulator of the immune system. It acts through two receptors resulting in often opposing biological effects, which may explain the lack of therapeutic potential obtained so far in multiple sclerosis (MS) with non-receptor-specific anti-TNF therapeutics. Under neuroinflammatory conditions, such as MS, TNF receptor-1 (TNFR1) is believed to mediate the pro-inflammatory activities associated with TNF, whereas TNF receptor-2 (TNFR2) may instead induce anti-inflammatory effects as well as promote remyelination and neuroprotection. In this study, we have investigated the therapeutic potential of blocking TNFR1 whilst simultaneously stimulating TNFR2 in a mouse model of MS.
Beschreibung:Gesehen am 10.08.2023
Beschreibung:Online Resource
ISSN:1742-2094
DOI:10.1186/s12974-023-02784-z