Author

C. Fourgeux

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

Biology Disciplines

Click to filter author papers

Immunology· 5

Signature Assays, Organisms & Methods

Click to filter · or open tag

Research Focus:cell type annotation· 4 Approach:experimental assay· 3 Organism:human· 3 Assay:scRNA-seq· 3 Approach:statistical model· 2 Assay:bulk RNA-seq· 1 Research Focus:cell-cell communication· 1 Research Focus:differential expression· 1

Frequent Co-Authors

J. Poschmann· 5 shared C. Guillonneau· 2 shared L. Bouchet-Delbos· 2 shared L. Brusselle· 2 shared R. Danger· 2 shared R. Josien· 2 shared S. Brouard· 2 shared S. REMY· 2 shared

Activity by Year

2020-2024 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 27 mutual co-author links

Click any collaborator node to inspect or filter shared papers

Focal author (center)Selected co-authorORCID co-authorUnlinked name

Curved chords = mutual co-authorship

5 shared papersImmunology

J. Poschmann

Mutual co-authors in cluster

Author profile →

5 papers

Recent·Most cited

The immune profile of circulating autoreactive CD4 T cells is imprinted through tissue activation during autoimmune liver diseases

A. Cardon, T. Guinebretiere, C. Dong, L. Gil, S. Ado, P.-j. Gavlovsky, M. Braud, R. Danger, C. Schultheiss, A. Domene, P. Paul-Gilloteaux, C. Chevalier, L. Bernier, J.-P. Judor, C. Fourgeux, , A. Renand

This study identifies the transcriptional profile of circulating autoreactive CD4 T cells in autoimmune liver diseases and shows their functional relationship to liver-specific pathogenic clones.

bioRxiv · Mar 26, 2024Immunology

Combinatory differentiation of human induced pluripotent stem cells generates thymic epithelium that supports thymic crosstalk and directs dendritic- and CD4/CD8 T-cell full development

N. Provin, M. d'Arco, E. Kervagoret, A. Bruneau, L. Brusselle, C. Fourgeux, J. Poschmann, X. Saulquin, C. Guillonneau, L. David, M. Giraud

This study generates functional thymic epithelial cells from iPSCs that support T cell development and dendritic cell differentiation in vitro.

bioRxiv · Dec 23, 2023Immunology

A gene-expression module in circulating immune cells is associated with cell migration during immune diseases.

D. Sinha, T. Laurent, A. Broquet, C. Fourgeux, T. Letellier, G. Tilly, S. Bruneau, S. Ville, L. Bouchet-Delbos, J. Branchereau, C. Kerleau, S. Brouard, G. Blancho, M. Giral, R. Josien, , J. Poschmann

The paper identifies a gene expression module in circulating immune cells linked to migration during immune diseases and shows its role in tissue recruitment and immune activation.

bioRxiv · Apr 11, 2023Immunology

CD4+ and CD8+ regulatory T cells characterization in the rat using a unique transgenic Foxp3-EGFP model.

S. MENORET, L. Tesson, S. REMY, V. Gourain, C. Serazin, C. Usal, A. Guiffes, V. Chenouard, L.-H. Ouisse, M. Gantier, J.-M. Heslan, C. Fourgeux, J. Poschmann, C. Guillonneau, I. Anegon

The paper develops a rat transgenic model with Foxp3-EGFP to study CD4+ and CD8+ regulatory T cells, revealing their frequencies, markers, suppressive activity, and transcriptome.

bioRxiv · Dec 9, 2021 · PreprintImmunology

Dendritic cells require TMEM176A/B ion channels for optimal MHC II antigen presentation to naive CD4+ T cells

M. Lancien, G. Bienvenu, L. Gueno, S. Salle, E. Merieau, S. Remy, A. Even, A. Moreau, A. Molle, C. Fourgeux, F. Coulon, G. Beriou, L. Bouchet-Delbos, E. Chiffoleau, P. Kirstetter, , C. Louvet

The paper shows TMEM176A/B ion channels are essential for dendritic cells to present antigens to CD4+ T cells, but not for Th17 or ILC3 function.

bioRxiv · May 1, 2020 · PreprintImmunology