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One-carbon metabolism sustains effector T cell function through cell-surface glycosylation.

Created on 25 Oct 2026

Authors

Peng Wang, Amy Yu, Mohammed Mutaher, Almut S Eisele, Sarah Mouche, Kaitlyn Hung, Reece C Larson, Madeline Gish, Margaret Zimmer, Jeanette R Brook, Miriam McNerney, Lea Hammer, Arjun Garg, Efrat Ozeri, Alan Y L Wong, Boryana Petrova, Michal Weitman, Ramon C Sun, Jerome Tamburini, Mathias Wenes, Marc Schwartz, Nir Hacohen, Naama Kanarek

Published in

bioRxiv : the preprint server for biology. Oct 07, 2026. Epub Oct 07, 2026.

Abstract

Folate is an essential driver of one-carbon metabolism. The cellular consequences of its deprivation in CD8 + T cell and impact on anti-tumor function are unknown. Single cell RNA-seq analysis of primary central nervous system lymphoma (PCNSL) patients' tumor samples revealed exhaustion in T cells with high folate metabolism gene expression signature. Functional genomics, metabolite profiling, and glycomics identified disrupted cell surface glycosylation as a major consequence of folate deprivation in CD8 + T cells. Mechanistically, folate deprivation reduced nucleotide sugar levels, perturbed glycosylation, and triggered the apoptotic unfolded protein response. Overexpressing folate transporters in adoptively transferred CD8 + T cells increased intratumoral T cell numbers and reduced exhaustion. Therefore, our data draw a mechanistic line between one-carbon metabolism, cell-surface glycosylation, and anti-tumor T cell function, and support a hypothesis that increased folate uptake can enhance CD8 + T cell function including ex vivo and in vivo CAR-T cells.
Although folate metabolism genes are highly expressed in both proliferating tumor and CD8 + T cells from primary central nervous system lymphoma patients, the T cells are exhausted while the tumor cells thrive Folate is depleted in the TME of MC38-OVA and B16-OVA tumors Folate deprivation impairs function and proliferation of CD8 + T cells Folate is essential for nucleotide sugar metabolism, and its depletion results in perturbation of cell surface glycosylationGenetic engineering to increase folate uptake by T cells increases intratumoral T cell numbers and reduces exhaustion.

PMID:
42926674
Bibliographic data and abstract were imported from PubMed on 25 Oct 2026.

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