Author

Rutger David Luteijn

University of California, BerkeleyORCID 0000-0002-6183-4573Unclaimed ORCID profile · follow to get notified of new preprints

Additional preprints under this name without ORCID

Rutger David Luteijn1 paper

Biology Disciplines

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Microbiology· 2 Immunology· 1

Signature Assays, Organisms & Methods

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Research Focus:cell type annotation· 2 Approach:experimental assay· 2 Organism:human· 2 Assay:bulk RNA-seq· 1 Research Focus:differential expression· 1 Research Focus:drug response / drug discovery· 1 Approach:genetic perturbation / CRISPR· 1 Research Focus:host-pathogen & immune response· 1

Frequent Co-Authors

David H. RauletiD· 2 shared Andia Moshari· 1 shared Collins Oduor OwinoiD· 1 shared Frank J. M. van KuppeveldiD· 1 shared Graham J. BelshamiD· 1 shared Hannah S. MartiniD· 1 shared Jeffery S. CoxiD· 1 shared Matthew B. FrancisiD· 1 shared

Activity by Year

2024-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 19 mutual co-author links

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2 shared papersImmunology

David H. RauletORCID

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3 papers

Recent·Most cited

Viral capsid delivery of cGAMP enhances STING-dependent antitumor immune response

Paul Huang, Yeara Jo, Hannah S. Martin, Rutger David Luteijn, David H. Raulet, Matthew B. Francis

This study shows that delivering cGAMP via bacteriophage MS2 nanoparticles enhances STING activation and antitumor immunity in mice.

bioRxiv · Jul 1, 2026 · PreprintImmunology

ITAF45 is a Pervasive Trans Acting Factor for Picornavirus Type II IRES Elements

Michael A. Bellucci, Mehdi Amiri, Stephen Berryman, Andia Moshari, Collins Oduor Owino, Rutger David Luteijn, Tobias J. Tuthill, Yuri V. Svitkin, Graham J. Belsham, Frank J. M. van Kuppeveld, Nahum Sonenberg

The paper identifies ITAF45 as a host factor essential for picornavirus Type II IRES-mediated translation, showing its role in multiple viruses and suggesting it as an antiviral target.

Proceedings of the National Academy of Sciences · Aug 11, 2025Peer-reviewedMicrobiology

UFMylation suppresses Type I IFN signaling during M. tuberculosis infection of human macrophages

Nicholas E. Garelis, Rutger David Luteijn, David H. Raulet, Jeffery S. Cox

The paper identifies UFMylation as a suppressor of Type I IFN signaling during M. tuberculosis infection of human macrophages through a CRISPR-interference screen.

bioRxiv · Aug 7, 2024 · PreprintMicrobiology