Exercise-induced microbiota metabolite enhances CD8 T cell antitumor immunity promoting immunotherapy efficacy

运动诱导的肠道菌群代谢产物增强CD8 T细胞抗肿瘤免疫力,从而提高免疫疗法的疗效。

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作者:Catherine M Phelps,Nathaniel B Willis,Tingting Duan,Amanda H Lee,Yue Zhang,Daphne M Rodriguez J,Surya P Pandey,Colin R Laughlin,Aaron B I Rosen,Alex C McPherson,Jake H Shapira,Simran K Randhawa,Lee Hedden,Tanner G Richie,Hallie M Wiechman,Mackenzie J Bender,Ina Nemet,Patrick A Zöhrer,Rachel A Gottschalk,Kathryn H Schmitz,Steven J Mullett,Stacy L Gelhaus,Diwakar Davar,Hassane M Zarour,Reinhard Hinterleitner,Thomas Mossington,Jonathan H Badger,Richard R Rodrigues,John A McCulloch,Sonny T M Lee,Karl-Heinz Wagner,Maria G Winter,Sebastian E Winter,Jishnu Das,Joseph F Pierre,Giorgio Trinchieri,Marlies Meisel

Abstract

Exercise improves immune checkpoint inhibitor (ICI) efficacy in cancers such as melanoma; however, the mechanisms through which exercise mediates this antitumor effect remain obscure. Here, we identify that the gut microbiota plays a critical role in how exercise improves ICI efficacy in preclinical melanoma. Our study demonstrates that exercise stimulates microbial one-carbon metabolism, increasing levels of the metabolite formate, which subsequently enhances cytotoxic CD8 T cell (Tc1)-mediated ICI efficacy. We further establish that microbiota-derived formate is both sufficient and required to enhance Tc1 cell fate in vitro and promote tumor antigen-specific Tc1 immunity in vivo. Mechanistically, we identify the transcription factor nuclear factor erythroid 2-related factor 2 (Nrf2) as a crucial mediator of formate-driven Tc1 function enhancement in vitro and a key player in the exercise-mediated antitumor effect in vivo. Finally, we uncover human microbiota-derived formate as a potential biomarker of enhanced Tc1-mediated antitumor immunity, supporting its functional role in melanoma suppression.

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