Author

S. L. Felce

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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Signature Assays, Organisms & Methods

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Approach:experimental assay· 2 Research Focus:host-pathogen & immune response· 2 Organism:human· 2 Assay:proteomics· 1

Frequent Co-Authors

G. Liu· 2 shared T. Dong· 2 shared X. Yao· 2 shared Y. Peng· 2 shared A. Chandran· 1 shared A. J. Mentzer· 1 shared A. Mayer· 1 shared A. McKnight· 1 shared

Activity by Year

2022-2022 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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2 shared papersImmunology

G. Liu

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2 papers

Recent·Most cited

Large clones of pre-existing T cells drive early immunity against SARS-COV-2 and LCMV infection.

M. Milighetti, Y. Peng, C. C. S. Tan, M. Mark, G. Nageswaran, S. Byrne, T. Ronel, T. Peacock, A. Mayer, A. Chandran, J. Rosenheim, M. Wheelan, X. Yao, G. Liu, S. L. Felce, , B. Chain

The paper identifies high frequency naive T cell precursors that drive rapid T cell responses during early SARS-COV-2 and LCMV infections.

bioRxiv · Nov 8, 2022Immunology

SARS-CoV-2 mutations affect proteasome processing to alter CD8+ T cell responses

D. Wellington, Z. Yin, Z. Yu, R. Heilig, S. Davis, R. Fischer, S. L. Felce, P. Hublitz, R. Beveridge, D. Dong, G. Liu, X. Yao, Y. Peng, B. M. M. Kessler, T. Dong

The paper investigates how mutations in flanking regions of SARS-CoV-2 nucleoprotein epitopes affect proteasome processing and CD8+ T cell responses, finding some mutations reduce responses while others enhance them.

bioRxiv · Apr 8, 2022 · PreprintImmunology