Author

T. Hoki

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

Biology Disciplines

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Research Focus:cell type annotation· 1 Research Focus:cell-cell communication· 1 Research Focus:differential expression· 1 Approach:experimental assay· 1 Assay:flow cytometry· 1 Research Focus:host-pathogen & immune response· 1 Organism:human· 1 Organism:mouse· 1

Frequent Co-Authors

F. Ito· 2 shared K. Attwood· 2 shared T. Oba· 2 shared T. Yamauchi· 2 shared B. H. Segal· 1 shared C. Morrison· 1 shared C. Xuefang· 1 shared G. Chatta· 1 shared

Activity by Year

2020-2020 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 40 mutual co-author links

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2 shared papersImmunology

F. Ito

Mutual co-authors in cluster

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2 papers

Recent·Most cited

CD40 and CD80/86 signaling in cDC1s mediate effective neoantigen vaccination and generation of antigen-specific CX3CR1+ CD8+ T cells in mice

T. Yamauchi, T. Hoki, T. Oba, K. Attwood, C. Xuefang, F. Ito

This study shows that CD40 and CD80/86 signaling in cDC1s enhances neoantigen vaccine efficacy and generates CX3CR1+ CD8+ T cells in mice.

bioRxiv · Jun 15, 2020Immunology

A circulating T-cell differentiation marker to predict response to immune checkpoint inhibitors

T. Yamauchi, T. Hoki, T. Oba, V. Jain, H. Chen, K. Attwood, S. Battaglia, S. George, G. Chatta, I. Puzanov, C. Morrison, K. Odunsi, B. H. Segal, G. K. Dy, M. S. Ernstoff, F. Ito

The paper identifies CX3CR1 expression on circulating CD8+ T cells as a biomarker predicting response to immune checkpoint inhibitor therapy in NSCLC patients.

bioRxiv · Jun 13, 2020Immunology