Author

S. Brackenridge

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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Immunology· 4

Signature Assays, Organisms & Methods

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Approach:experimental assay· 4 Research Focus:host-pathogen & immune response· 4 Organism:human· 4 Assay:proteomics· 3 Organism:rat· 2 Research Focus:drug response / drug discovery· 1 Organism:mouse· 1 Assay:protein structure· 1

Frequent Co-Authors

P. Borrow· 4 shared A. J. McMichael· 3 shared A. McMichael· 1 shared B. F. Haynes· 1 shared D. Li· 1 shared D. Rozbesky· 1 shared D. W. Cain· 1 shared E. Brenna· 1 shared

Activity by Year

2020-2022 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 27 mutual co-author links

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4 shared papersImmunology

P. Borrow

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4 papers

Recent·Most cited

Regulation of the cell surface expression of classical and non-classical MHC proteins by the human cytomegalovirus UL40 and rhesus cytomegalovirus Rh67 proteins

S. Brackenridge, P. Borrow, A. McMichael

This paper shows that UL40 and Rh67 proteins from CMV replace endogenous VL9 peptides to up-regulate MHC-E expression, enabling immune evasion by NK cells.

bioRxiv · Jul 22, 2022Immunology

Mapping the epitopes of the Human Leukocyte Antigen E antibodies 3D12 and 4D12

S. Brackenridge, P. Borrow, A. J. McMichael

This study maps the epitopes of antibodies 3D12 and 4D12 that bind to HLA-E, revealing distinct binding regions on the alpha 3 and alpha 2 domains.

bioRxiv · May 27, 2022Immunology

Mouse and Human Antibodies that Bind HLA-E-Leader Peptide Complexes and Enhance NK Cell Cytotoxicity

D. Li, S. Brackenridge, L. C. Walters, O. Swanson, K. Harlos, D. Rozbesky, D. W. Cain, K. Wiehe, R. M. Scearce, M. Barr, Z. Mu, R. Parks, M. Quastel, R. J. Edwards, Y. Wang, , B. F. Haynes

The paper isolates antibodies that bind HLA-E-Leader peptide complexes and enhance NK cell cytotoxicity in both mice and humans.

bioRxiv · Dec 3, 2020Immunology

HLA-E restricted, HIV-1 suppressing, Gag specific CD8+ T cells offer universal vaccine opportunities

H. Yang, M. Rei, S. Brackenridge, E. Brenna, H. Sun, s. abdulhaqq, M. K. Liu, W. Ma, P. Kurupati, x. Xu, V. Cerundolo, E. Jenkins, S. J. Davis, J. B. Sacha, K. Frueh, , A. J. McMichael

The paper demonstrates that HLA-E restricted, HIV-1 specific CD8+ T cells can suppress HIV-1 replication in vitro, suggesting potential for a universal vaccine.

bioRxiv · Dec 1, 2020 · PreprintImmunology