Author

S. J. Redmond

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

Biology Disciplines

Click to filter author papers

Immunology· 2

Signature Assays, Organisms & Methods

Click to filter · or open tag

Approach:experimental assay· 2 Approach:biophysical modeling· 1 Research Focus:cell signaling & trafficking· 1 Research Focus:cell type annotation· 1 Assay:flow cytometry· 1 Research Focus:host-pathogen & immune response· 1 Organism:human· 1 Research Focus:protein structure prediction· 1

Frequent Co-Authors

A. P. Uldrich· 2 shared D. I. Godfrey· 2 shared N. A. Gherardin· 2 shared R. Seneviratna· 2 shared S. Li· 2 shared A. Behren· 1 shared A. Chung· 1 shared A. Hammet· 1 shared

Activity by Year

2021-2023 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 41 mutual co-author links

Click any collaborator node to inspect or filter shared papers

Focal author (center)Selected co-authorORCID co-authorUnlinked name

Curved chords = mutual co-authorship

2 shared papersImmunology

A. P. Uldrich

Mutual co-authors in cluster

Author profile →

2 papers

Recent·Most cited

Vgamma9Vdelta2 T cells recognize butyrophilin 2A1 and 3A1 heteromers

T. S. Fulford, C. Soliman, R. G. Castle, M. Rigau, Z. Ruan, O. Dolezal, R. Seneviratna, H. G. Brown, E. Hanssen, A. Hammet, S. Li, S. J. Redmond, A. Chung, M. A. Gorman, M. W. Parker, , A. P. Uldrich

The paper reveals that Vgamma9Vdelta2 T cells recognize BTN2A1 and BTN3A1 heteromers through dual epitope engagement, uncovering a new mechanism of immune activation.

bioRxiv · Aug 30, 2023Immunology

CD36 family members are TCR-independent ligands for CD1 antigen-presentingmolecules

N. A. Gherardin, S. J. Redmond, H. E. McWilliam, C. F. Almeida, K. H. Gourley, R. Seneviratna, S. Li, R. De Rose, C. V. Nguyen-Robertson, S. Su, M. Ritchie, J. A. Villadangos, D. B. Moody, D. G. Pellicci, A. P. Uldrich, D. I. Godfrey

The paper identifies CD36 family members as ligands for CD1 molecules and shows that blocking this interaction enables accurate identification of CD1-restricted T cells.

bioRxiv · Mar 10, 2021Immunology