Author

W. Richer

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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Signature Assays, Organisms & Methods

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Organism:mouse· 4 Assay:bulk RNA-seq· 3 Approach:experimental assay· 3 Research Focus:cell type annotation· 2 Assay:flow cytometry· 2 Research Focus:host-pathogen & immune response· 2 Organism:human· 2 Research Focus:cancer & tumor microenvironment· 1

Frequent Co-Authors

E. Piaggio· 3 shared J. Tosello boari· 3 shared A. Gruppi· 2 shared C. L. Montes· 2 shared C. Rodriguez· 2 shared C. Sedlik· 2 shared M. C. Ramello· 2 shared P. Caudana· 2 shared

Activity by Year

2018-2024 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 32 mutual co-author links

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3 shared papersImmunology

E. Piaggio

Mutual co-authors in cluster

Author profile →

4 papers

Recent·Most cited

TNFR2 blockade promotes anti-tumoral immune response in PDAC by targeting activated Treg and reducing T cell exhaustion

A. Debesset, C. Pilon, S. Meunier, O. Bonizec, W. Richer, A. Thiolat, C. Houppe, M. Ponzo, J. Magnan, P. Caudana, J. Tosello boari, S. Baulande, N. H. To, B. L. Salomon, E. Piaggio, , J. L. Cohen

This study shows that blocking TNFR2 reduces Treg activity and T cell exhaustion in PDAC, with improved efficacy when combined with CD40 agonists.

bioRxiv · Jan 22, 2024 · PreprintImmunology

CD39+ conventional CD4+ T cells with exhaustion traits and cytotoxic potential infiltrate tumors and expand upon CTLA-4 blockade

S. N. Bossio, C. Abrate, J. Tosello Boari, C. Rodriguez, F. Canale, M. C. Ramello, W. Richer, D. Rocha, C. Sedlik, A. Salomon, E. Borcoman, A. del Castillo, A. Gruppi, E. Fernandez, E. V. Acosta Rodriguez, C. L. Montes

The paper identifies CD39+ CD4+ T cells in tumors with exhaustion and cytotoxic traits, showing their expansion with CTLA-4 blockade and association with better survival in breast cancer.

bioRxiv · Jan 30, 2023Immunology

Tissue-resident FOLR2+ macrophages associate with tumor-infiltrating CD8+ T cells and with increased survival of breast cancer patients.

R. N. Ramos, Y. Missolo-Koussou, Y. Gerber-Ferder, C. Bromley, M. Bugatti, N. G. Nunez, J. Boari Tosello, W. Richer, J. Denizeau, C. Sedlik, P. Caudana, F. Kotsias, L. L. Niborski, S. Viel, M. Bohec, , J. Helft

The paper identifies FOLR2+ macrophages in breast cancer that correlate with improved patient survival and co-localize with CD8+ T cells across multiple cancers.

bioRxiv · Apr 12, 2021 · PreprintImmunology

IL-17RA-signaling modulates CD8+ T cell survival and exhaustion during Trypanosoma cruzi infection

J. Tosello Boari, C. L. Araujo Furlan, F. Fiocca Vernengo, C. Rodriguez, M. C. Ramello, M. C. Amezcua Vesely, M. Gorosito Serran, N. G. Nuñez, W. Richer, E. Piaggio, C. L. Montes, A. Gruppi, E. Acosta Rodriguez

This study shows that IL-17RA-signaling supports CD8+ T cell survival and function during Trypanosoma cruzi infection, with its absence leading to increased parasite load and reduced T cell responses.

bioRxiv · May 11, 2018Immunology