Author

Sarah Bennett

University of North Carolina at Chapel HillORCID 0000-0002-4605-2776Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Cancer Biology· 1 Immunology· 1

Signature Assays, Organisms & Methods

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Approach:experimental assay· 2 Organism:human· 2 Research Focus:cell type annotation· 1 Assay:CITE-seq· 1 Research Focus:drug response / drug discovery· 1 Assay:proteomics· 1

Frequent Co-Authors

Alex RubinsteyniD· 2 shared Jessica Alley· 2 shared Mitra ShabrangiD· 2 shared Amber Smith· 1 shared B. V. Vincent· 1 shared Benjamin Garrett VincentiD· 1 shared Brandon A. PriceiD· 1 shared Brian A. KuhlmaniD· 1 shared

Activity by Year

2026-2026 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 35 mutual co-author links

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2 shared papersImmunology

Alex RubinsteynORCID

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2 papers

Recent·Most cited

ImmunologybioRxivPreprintOct 15, 2026

Discovery of frameshift-associated TCRs following personalized neoantigen vaccination in a patient with osteosarcoma

Sarah Bennett, Jessica Alley, Mitra Shabrang…·Benjamin Garrett Vincent

The paper reports the discovery of TCRs specific to vaccine peptides in a patient with osteosarcoma following personalized neoantigen vaccination and in vitro expansion.

DOI 10.64898/2026.10.09.757920

humanCITE-seq

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Cancer BiologyJournal for ImmunoTherapy of CancerPeer-reviewedFeb 1, 2026

Shared PRAME Epitopes are T-Cell Targets in NUT Carcinoma

Jeffrey Lee Jensen, Sara K. Peterson, Maria J. Sambade…·B. V. Vincent

This study identifies PRAME as a therapeutic target in NUT carcinoma, showing its high expression and susceptibility to T-cell mediated cytotoxicity via PRAME epitopes presented by HLA Class I molecules.

5 citationstop 3%

humanproteomics

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