Author

S. Vicente-Munoz

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

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Immunology· 1

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Research Focus:cancer & tumor microenvironment· 1 Research Focus:cell signaling & trafficking· 1 Approach:experimental assay· 1 Organism:human· 1 Research Focus:metabolism & bioenergetics· 1 Assay:metabolomics· 1

Frequent Co-Authors

A. N. Lane· 1 shared E. Miller· 1 shared H. Sun· 1 shared J. R. Gnanaprakasam· 1 shared L. Liu· 1 shared M. O. Warmoes· 1 shared Q. Sun· 1 shared R. Wang· 1 shared

Activity by Year

2019-2019 · peak 1/yr

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10 top collaborators · 45 mutual co-author links

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1 shared paperImmunology

A. N. Lane

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1 paper

Recent·Most cited

Inosine is an alternative carbon supply that supports effector T cell proliferation and anti-tumor function under glucose restriction

T. Wang, J. R. Gnanaprakasam, X. Chen, S. Kang, X. Xu, H. Sun, L. Liu, E. Miller, T. A. Cassel, Q. Sun, S. Vicente-Munoz, M. O. Warmoes, A. N. Lane, X. Song, T. W.- M. Fan, R. Wang

This study shows that effector T cells use inosine as an alternative carbon source under glucose restriction, enhancing anti-tumor function and bypassing tumor-imposed metabolic limitations.

bioRxiv · Sep 14, 2019 · PreprintImmunology