C
Christophe Caux
Researcher at French Institute of Health and Medical Research
Publications - 254
Citations - 32907
Christophe Caux is an academic researcher from French Institute of Health and Medical Research. The author has contributed to research in topics: Immune system & Dendritic cell. The author has an hindex of 74, co-authored 232 publications receiving 30760 citations. Previous affiliations of Christophe Caux include Centre national de la recherche scientifique & International Facility Management Association.
Papers
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Journal ArticleDOI
Langerin : une nouvelle lectine spécifique des cellules de Langerhans induit la formation de granules de Birbeck
TL;DR: Le gene codant la Langerin humaine transfecte dans des cellules d'une lignee fibroblastique de souris induit la formation des granules de Birbeck and devrait permettre the comprehension of the fonction de ces granules of Birbeck.
Patent
Cd73 blocking agents
Christophe Caux,Laurent Gauthier,Nicolas Gourdin,Christine Ménétrier-Caux,Carine Paturel,Ivan Perrot +5 more
TL;DR: In this article, the authors have shown that antibodies that bind and inhibit CD73, are capable of increasing the proliferation of T cells in the presence of CD39-expressing B cells and ATP.
Journal ArticleDOI
Autocrine role for Gas6 with Tyro3 and Axl in leiomyosarcomas
Hiba El Sayadi,Daniel Pissaloux,Laurent Alberti,Séverine Tabone-Eglinger,Dominique Ranchère,Anne Valérie Decouvelaere,Eric Tabone,Isabelle Ray-Coquard,Christophe Caux,Jérôme Fayette,Jean-Yves Blay +10 more
TL;DR: To identify novel altered pathways in LMS, which may be of therapeutic value for patients, fresh frozen samples of soft tissue and visceral LMS were analyzed and compared with normal smooth muscle uterine tissue (NSM) for phosphoproteomic profile.
Book ChapterDOI
Human Dendritic Cells Enhance Growth and Differentiation of CD40 Activated B Cells
Bertrand Dubois,Jérôme Fayette,Béatrice Vanbervliet,Jacques Banchereau,Francine Brière,Christophe Caux +5 more
TL;DR: D-Lc enhanced both CD40-L dependent B cell proliferation and Ig productions, and allowed low numbers of B cells to produce detectable amounts of Igs in presence of exogenous cytokine such as IL-10.