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Projekt Druckansicht

Die Rolle von c-Rel und IkappaBNS bei der T-Zell-Aktivierung und der Differenzierung follikulärer T-Zellen

Fachliche Zuordnung Immunologie
Förderung Förderung von 2015 bis 2024
Projektkennung Deutsche Forschungsgemeinschaft (DFG) - Projektnummer 268984183
 
Erstellungsjahr 2025

Zusammenfassung der Projektergebnisse

Our previous work demonstrated the role of IκBNS, an atypical inhibitor of NF-κB, in T cell proliferation and the differentiation of distinct CD4+ T helper (Th) cell subsets, including Th1, Th17, and regulatory T cells (Tregs). Th1 and Th17 cells require strong T cell receptor (TCR) signaling for their differentiation. Of note, IκBNS is strongly induced upon TCR activation. Follicular helper T cells (Tfh) represent a specialized subset of Th cells that play a crucial role in the humoral immune response by supporting B cell proliferation and differentiation into antibody-producing cells within germinal centers (GC). Tfh cell differentiation is driven by constitutively TCR signaling, both during their development and functional activity. The differentiation process occurs in a stepwise manner: first, through antigen presentation, leading to the generation of precursor Tfh cells (pre-Tfh), and later through interaction with cognate B cells, allowing full maturation into GC Tfh cells. Within the germinal center, GC Tfh cells promote B cell proliferation and antibody affinity maturation via receptor-ligand interactions, such as TCR-MHC II, ICOS-ICOSL, and CD40L-CD40 signaling, as well as through cytokine production and signaling, such as IL-21. Given the constant TCR stimulation required for Tfh differentiation and function, we hypothesized that IκBNS would be highly induced in Tfh cells and play a critical role in their development and function. As outlined in our DFG proposal, we aimed to investigate the role of IκBNS in Tfh differentiation across different organs, such as the spleen and Peyer’s patches.

Projektbezogene Publikationen (Auswahl)

 
 

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