Author

F. Ossendorp

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· 3

Signature Assays, Organisms & Methods

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Research Focus:cell type annotation· 2 Approach:experimental assay· 2 Research Focus:host-pathogen & immune response· 2 Organism:mouse· 2 Research Focus:cell signaling & trafficking· 1 Assay:CITE-seq· 1 Approach:deep learning· 1 Research Focus:differential expression· 1

Frequent Co-Authors

E. Beyranvand Nejad· 2 shared E. T. I. van der Gracht· 2 shared G. Beyrend· 2 shared K. L. M. C. Franken· 2 shared M. G. M. Camps· 2 shared R. Arens· 2 shared S. van Duikeren· 2 shared T. Abdelaal· 2 shared

Activity by Year

2019-2021 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 44 mutual co-author links

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2 shared papersImmunology

E. Beyranvand Nejad

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Author profile →

3 papers

Recent·Most cited

OX40 agonism enhances efficacy of PD-L1 checkpoint blockade by shifting the cytotoxic T cell differentiation spectrum

G. Beyrend, T. C. van der Sluis, E. T. I. van der Gracht, T. Abdelaal, S. P. Jochems, R. A. Belderbos, T. H. Wesselink, S. van Duikeren, F. J. van Haften, A. Redeker, E. Beyranvand Nejad, M. Camps, K. L. M. C. Franken, M. M. Linssen, P. Hohenstein, , R. Arens

This study shows that OX40 agonism improves PD-L1 checkpoint blockade by altering T cell differentiation, leading to enhanced anti-tumor immunity through dynamic expression of NK and chemokine receptors.

bioRxiv · Dec 24, 2021 · PreprintImmunology

A third vaccination with a single T cell epitope protects against SARS-CoV-2 infection in the absence of neutralizing antibodies

I. N. Pardieck, E. T. I. van der Gracht, D. M. B. Veerkamp, F. M. Behr, S. van Duikeren, G. Beyrend, J. Rip, R. Nadafi, T. C. van der Sluis, E. Beyranvand Nejad, N. Mulling, D. J. Brasem, M. G. M. Camps, S. K. Myeni, P. J. Bredenbeek, , R. Arens

A third dose of a single T cell epitope vaccine protects mice from SARS-CoV-2 infection without neutralizing antibodies by enhancing effector-memory and tissue-resident memory T cells.

bioRxiv · Dec 15, 2021 · PreprintImmunology

Bioorthogonal antigens allow the unbiased study of antigen processing and presentation

C. Araman, L. Pieper-Pournara, T. van Leeuwen, A. S. B. Kampstra, T. Bakkum, M. H. S. Marqvorsen, C. Nascimento, W. van der Wulp, M. G. J. M. Groenewold, M. G. M. Camps, H. S. Overkleeft, F. Ossendorp, R. Toes, S. I. van Kasteren

The paper explores how bioorthogonal antigens can be used to study antigen processing and presentation without bias.

bioRxiv · Jun 4, 2019 · PreprintImmunology