Author

B. J. Van den Eynde

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· 2 Cell Biology· 1

Signature Assays, Organisms & Methods

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Research Focus:cell type annotation· 3 Approach:experimental assay· 2 Organism:mouse· 2 Assay:proteomics· 2 Research Focus:cell signaling & trafficking· 1 Assay:CITE-seq· 1 Research Focus:clustering· 1 Approach:deep learning· 1

Frequent Co-Authors

S. Naulaerts· 2 shared A. A. Martinez· 1 shared A. D. Garg· 1 shared A. Jainarayanan· 1 shared A. Liston· 1 shared A. V. Hill· 1 shared A. Wicki· 1 shared C. A. Opitz· 1 shared

Activity by Year

2021-2023 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 15 mutual co-author links

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2 shared papersCell Biology

S. Naulaerts

Mutual co-authors in cluster

Author profile →

3 papers

Recent·Most cited

ImmunologybioRxivPreprintDec 18, 2023

Chemotherapy synergizes with cancer vaccines and expands stem-like TCF1+CD8+ T cells

L. Noblecourt, A. Wicki, V. Pereira-Almeida…·C. S. K. Leung

This study shows that chemotherapy, specifically CarboTaxol, synergizes with cancer vaccines and anti-PD-1 to improve tumor control and survival by expanding stem-like TCF1+CD8+ T cells.

DOI 10.1101/2023.12.18.572068

mouseCITE-seq

𝕏 PostBluesky

Cell BiologybioRxivJan 16, 2023

Tryptophan depletion sensitizes the AHR pathway by increasing AHR expression and GCN2/LAT1-mediated kynurenine uptake, and potentiates induction of regulatory T lymphocytes

M. Solvay, P. Pfander, S. Klaessens…·J. Zhu

This study shows that tryptophan depletion increases AHR expression and kynurenine uptake, enhancing AHR activation and promoting regulatory T cell differentiation.

DOI 10.1136/jitc-2023-006728

mouseproteomics

𝕏 PostBluesky

ImmunologybioRxivNov 22, 2021

Immunogenomic, single-cell and spatial dissection of CD8+T cell exhaustion reveals critical determinants of cancer immunotherapy

S. Naulaerts, D. M. Borras, A. A. Martinez…·A. D. Garg

This study identifies distinct CD8+T cell states in cancer patients using multi-omics data, showing that dysfunctional states resist immunotherapy while exhausted states can be targeted with specific treatments.

DOI 10.1126/scitranslmed.add1016

humanscRNA-seq

𝕏 PostBluesky