Author

M. Cavazzana

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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Approach:experimental assay· 3 Organism:human· 3 Research Focus:cell type annotation· 2 Research Focus:differential expression· 2 Assay:bulk RNA-seq· 1 Research Focus:cell signaling & trafficking· 1 Research Focus:development & morphogenesis· 1 Assay:flow cytometry· 1

Frequent Co-Authors

E. Six· 2 shared F. Rieux-Laucat· 2 shared I. Andre· 2 shared J. Zuber· 2 shared M. Delville· 2 shared A. Belot· 1 shared A. Bouafia· 1 shared A. Magerus· 1 shared

Activity by Year

2020-2020 · peak 3/yr

Co-Author Collaboration Network

10 top collaborators · 24 mutual co-author links

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2 shared papersImmunology

E. Six

Mutual co-authors in cluster

Author profile →

3 papers

Recent·Most cited

CD28 costimulatory domain protects against tonic signaling-induced functional impairment in CAR-Tregs

B. Lamarthee, A. Marchal, S. Charbonnier, T. Blein, E. Martin, K. Vogt, M. Titeux, M. Delville, H. Vincon, E. Six, N. Pallet, D. Anglicheau, C. Legendre, J.-L. Taupin, B. Sawitzki, , J. Zuber

This study compares CD28 and 4-1BB costimulatory domains in CAR-Tregs, finding CD28 better preserves function and survival under tonic signaling.

bioRxiv · Nov 19, 2020 · PreprintImmunology

Single cell analysis of FOXP3 deficiencies in humans and mice unmasks intrinsic and extrinsic CD4+ T cell perturbations

D. Zemmour, L.-M. Charbonnier, J. Leon, E. Six, S. Keles, M. Delville, S. Baris, J. Zuber, K. Chen, B. Neven, M. I. Garcia-Lloret, F. Ruemmele, C. B. Brugnara, N. Cerf-Bensussan, F. Rieux-Laucat, , C. Benoist

The paper analyzes FOXP3 deficiencies in humans and mice using single-cell RNA-seq and flow cytometry to uncover intrinsic and extrinsic CD4+ T cell perturbations in IPEX syndrome.

bioRxiv · Jul 6, 2020Immunology

Heterozygous RELA mutations cause early-onset systemic lupus erythematosus by hijacking the NF-κB pathway towards transcriptional activation of type-I Interferon genes

L. Barnabei, H. Lamrini, M. Castela, N. Jeremiah, M.-C. Stolzenberg, L. Chentout, S. Mirshavalad, A. Bouafia, A. Magerus, M. Moncan, S. Jacques, O. Pelle, V. Bondet, D. Duffy, M. Parisot, , F. Rieux-Laucat

This study identifies heterozygous RELA mutations in early-onset SLE patients, showing they drive type-I interferon gene expression through NF-κB pathway hijacking.

bioRxiv · Apr 27, 2020 · PreprintImmunology