Trans-vaccenic acid reprograms CD8+ T cells and anti-tumour immunity

Fan, Hao; Xia, Siyuan; Xiang, Junhong; Li, Yuancheng; Ross, Matthew O.; Lim, Seon Ah; Yang, Fan; Tu, Jiayi; Xie, Lishi; Dougherty, Urszula; Zhang, Freya Q.; Zheng, Zhong; Zhang, Rukang; Wu, Rong; Dong, Lei; Su, Rui; Chen, Xiufen; Althaus, Thomas; Riedell, Peter A.; Jonker, Patrick B.; Muir, Alexander; Stock, Wendy; Odenike, Olatoyosi; Patel, Anand A.; Tsuji, Takemasa; Matsuzaki, Junko; Shah, Hardik; Faubert, Brandon; Elf, Shannon E.; Bissonnette, B. Marc; He, Yu-Ying; Kline, Justin; Odunsi, Kunle; Gao, Xue; He, Chuan; Chen, Jing

doi:10.6082/3972p-e1t95

Published November 22, 2023 | Version v1

Journal article Open

Trans-vaccenic acid reprograms CD8+ T cells and anti-tumour immunity

1. University of Chicago
2. Emory University
3. St Jude Children's Research Hospital
4. City of Hope

Diet-derived nutrients are inextricably linked to human physiology by providing energy and biosynthetic building blocks and by functioning as regulatory molecules. However, the mechanisms by which circulating nutrients in the human body influence specific physiological processes remain largely unknown. Here we use a blood nutrient compound library-based screening approach to demonstrate that dietary trans-vaccenic acid (TVA) directly promotes effector CD8⁺ T cell function and anti-tumour immunity in vivo. TVA is the predominant form of trans-fatty acids enriched in human milk, but the human body cannot produce TVA endogenously. Circulating TVA in humans is mainly from ruminant-derived foods including beef, lamb and dairy products such as milk and butter, but only around 19% or 12% of dietary TVA is converted to rumenic acid by humans or mice, respectively. Mechanistically, TVA inactivates the cell-surface receptor GPR43, an immunomodulatory G protein-coupled receptor activated by its short-chain fatty acid ligands. TVA thus antagonizes the short-chain fatty acid agonists of GPR43, leading to activation of the cAMP–PKA–CREB axis for enhanced CD8⁺ T cell function. These findings reveal that diet-derived TVA represents a mechanism for host-extrinsic reprogramming of CD8⁺ T cells as opposed to the intrahost gut microbiota-derived short-chain fatty acids. TVA thus has translational potential for the treatment of tumours.

Notes

Due to the large number of authors, only the first 20 and the University of Chicago authors are included on the above author list. Please download the article for the complete list of authors.

Data availability

The 16S amplicon sequencing data have been deposited at the Gene Expression Omnibus (GEO) with the accession number GSE202266. The KAS-seq data have been deposited at the GEO repository with the accession number GSE202730. The RNA-seq data have been deposited at the GEO repository with the accession number GSE202276 and GSE202274. All data supporting the findings of this study are available within the Article and its Supplementary Information. Source data are provided with this paper.

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