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Projekt Druckansicht

Die Rolle von follikulären T-Helferzellen in T-Helferzell-Differenzierung, Funktion und Plastizität

Fachliche Zuordnung Immunologie
Förderung Förderung von 2014 bis 2021
Projektkennung Deutsche Forschungsgemeinschaft (DFG) - Projektnummer 252623821
 
Erstellungsjahr 2021

Zusammenfassung der Projektergebnisse

T follicular helper (Tfh) cells provide essential help to B cells for potent antibody responses. Tfh cells have also emerged as central intermediaries of other CD4+ T cell-mediated immune responses that involve the generation of certain effector and memory T helper cells. However, the precise relationships between these T helper cells remain unknown. This Emmy Noether research project aimed at dissecting the molecular and cellular requirements for the differentiation and maintenance of Tfh cells and other T helper cell subsets. We here dissected the role of the miR-17~92 cluster during Th17 cell differentiation and identified miR-18a as a potent inhibitor of Th17 cells. To address the role of miRNAs in the maintenance of Tfh cells, we developed a versatile experimental system that allowed the induced deletion of all mature miRNAs specifically in CD4+ T cells through deletion of Dgcr8, which is required for miRNA biogenesis. We found that two mouse strains containing such a CD4-CreERT2 construct differed substantially in their feasibility for these studies. Induced Dgcr8 deficiency during an ongoing immune response resulted in reduced Tfh cell frequencies and germinal centers (GCs). Besides deletion of miRNAs, we also used this system to ablate the Tfh-associated chemokine receptor Cxcr5 as well as the transcription factor Bcl6, in already differentiated Tfh cells. Induced ablation of Cxcr5 had minor effects on the function of established Tfh cells and Cxcr5-ablated cells still exhibited most features of CXCR5-positive Tfh cells. In contrast, continued Bcl6 expression was critical to maintain the GC Tfh cell phenotype and also the GC reaction. Importantly, T cell-specific Bcl6 ablation during acute viral infection resulted in transdifferentiation of established Tfh into Th1 cells, thus underlining the high degree of Tfh cell plasticity. Taken together, this project contributed to a better understanding of how Tfh cells are regulated on the molecular level and how Tfh cells contribute to T helper cell fate decisions, which could be leveraged in the future to target Tfh cells in autoimmune diseases or boost their function in infections and vaccination.

Projektbezogene Publikationen (Auswahl)

 
 

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