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Metabolic reprogramming of naïve regulatory T cells by IL-7 and IL-15 promotes their persistence and performance upon adoptive transfer

Academic Article
Publication Date:
2025
Short description:
Metabolic reprogramming of naïve regulatory T cells by IL-7 and IL-15 promotes their persistence and performance upon adoptive transfer / Filoni, J.; Ferrari, A.; Jofra, T.; Putignano, A. R.; Da Dalt, L.; Cesarano, S.; Di Dedda, C.; Bonacina, F.; Marchesi, F.; Norata, D.; Bonini, C.; Piemonti, L.; Monti, P.. - In: COMMUNICATIONS BIOLOGY. - ISSN 2399-3642. - 8:1(2025). [10.1038/s42003-024-07381-1]
abstract:
Tregs for adoptive therapy are traditionally expanded ex vivo using high doses of IL-2. However, the final Treg product has limited survival once infused in patients, potentially affecting therapeutic effectiveness. Here, we tested a novel expansion protocol in which highly purified naïve Tregs were expanded with a combination of IL-7 and IL-15, in the absence of IL-2. The final Treg product was enriched with cells displaying an immature CD45RA+CD62L+CD95+ phenotype, reminiscent of conventional memory stem T cells. The combination of IL-7 and IL-15 confers Tregs a glycolytic metabolism and improved metabolic fitness, characterized by an increased capacity to adapt metabolism according to glucose and oxygen availability. Tregs expanded with IL-7 and IL-15 showed longer persistence and an improved capacity to control xeno-GvHD in NSG mice. This work suggests that metabolic reprogramming induced by IL-7 and IL-15 provides better Treg performance for adoptive therapy.
Iris type:
1.1 Articolo in rivista
List of contributors:
Filoni, J.; Ferrari, A.; Jofra, T.; Putignano, A. R.; Da Dalt, L.; Cesarano, S.; Di Dedda, C.; Bonacina, F.; Marchesi, F.; Norata, D.; Bonini, C.; Piemonti, L.; Monti, P.
Authors of the University:
BONINI MARIA CHIARA
PIEMONTI LORENZO
Handle:
https://iris.unisr.it/handle/20.500.11768/180761
Full Text:
https://iris.unisr.it//retrieve/handle/20.500.11768/180761/290813/42003_2024_Article_7381.pdf
Published in:
COMMUNICATIONS BIOLOGY
Journal
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URL

https://www.nature.com/articles/s42003-024-07381-1
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