Phelps Catherine M, Willis Nathaniel B, Duan Tingting, Lee Amanda H, Zhang Yue, Rodriguez J Daphne M, Pandey Surya P, Laughlin Colin R, Rosen Aaron B I, McPherson Alex C, Shapira Jake H, Randhawa Simran K, Hedden Lee, Richie Tanner G, Wiechman Hallie M, Bender Mackenzie J, Nemet Ina, Zöhrer Patrick A, Gottschalk Rachel A, Schmitz Kathryn H, Mullett Steven J, Gelhaus Stacy L, Davar Diwakar, Zarour Hassane M, Hinterleitner Reinhard, Mossington Thomas, Badger Jonathan H, Rodrigues Richard R, McCulloch John A, Lee Sonny T M, Wagner Karl-Heinz, Winter Maria G, Winter Sebastian E, Das Jishnu, Pierre Joseph F, Trinchieri Giorgio, Meisel Marlies
Department of Immunology, University of Pittsburgh School of Medicine, Pittsburgh, PA, USA; Graduate Program of Microbiology and Immunology, University of Pittsburgh School of Medicine, Pittsburgh, PA, USA.
Department of Nutritional Sciences, University of Wisconsin-Madison, Madison, WI, USA.
Cell. 2025 Jul 4. doi: 10.1016/j.cell.2025.06.018.
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.
运动可提高免疫检查点抑制剂(ICI)对黑色素瘤等癌症的疗效;然而,运动介导这种抗肿瘤作用的机制仍不清楚。在这里,我们发现肠道微生物群在运动如何提高临床前黑色素瘤中ICI疗效方面起着关键作用。我们的研究表明,运动刺激微生物一碳代谢,增加代谢物甲酸的水平,随后增强细胞毒性CD8 T细胞(Tc1)介导的ICI疗效。我们进一步证实,微生物群衍生的甲酸在体外增强Tc1细胞命运和在体内促进肿瘤抗原特异性Tc1免疫方面既是充分的也是必需的。从机制上讲,我们确定转录因子核因子红细胞2相关因子2(Nrf2)是体外甲酸驱动的Tc1功能增强的关键介质,也是体内运动介导的抗肿瘤作用的关键参与者。最后,我们发现人类微生物群衍生的甲酸是增强Tc1介导的抗肿瘤免疫的潜在生物标志物,支持其在黑色素瘤抑制中的功能作用。