M
Mikael Ebbo
Researcher at Aix-Marseille University
Publications - 117
Citations - 4359
Mikael Ebbo is an academic researcher from Aix-Marseille University. The author has contributed to research in topics: Medicine & Rituximab. The author has an hindex of 27, co-authored 85 publications receiving 2857 citations. Previous affiliations of Mikael Ebbo include University of the Mediterranean.
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Journal ArticleDOI
Association of COVID-19 inflammation with activation of the C5a-C5aR1 axis.
Julien Carvelli,Olivier Demaria,Frédéric Vély,Luciana Batista,Nassima Chouaki Benmansour,Joanna Fares,Sabrina Carpentier,Marie-Laure Thibult,Ariane Morel,Romain Remark,Pascale Andre,Agnès Represa,Christelle Piperoglou,Pierre Yves Cordier,Erwan Le Dault,Christophe Guervilly,Pierre Simeone,Marc Gainnier,Yannis Morel,Mikael Ebbo,Nicolas Schleinitz,Eric Vivier +21 more
TL;DR: Results suggest that blockade of the C5a–C5aR1 axis could be used to limit the infiltration of myeloid cells in damaged organs and prevent the excessive lung inflammation and endothelialitis that are associated with acute respiratory distress syndrome in patients with COVID-19.
Journal ArticleDOI
High-Dimensional Single-Cell Analysis Identifies Organ-Specific Signatures and Conserved NK Cell Subsets in Humans and Mice
Adeline Crinier,Pierre Milpied,Bertrand Escalière,Christelle Piperoglou,Justine Galluso,Anaïs Balsamo,Lionel Spinelli,Inaki Cervera-Marzal,Mikael Ebbo,Mathilde J. H. Girard-Madoux,Sébastien Jaeger,Emilie Bollon,Sami Hamed,Jean Hardwigsen,Sophie Ugolini,Frédéric Vély,Emilie Narni-Mancinelli,Eric Vivier +17 more
TL;DR: Using high‐throughput single‐cell RNA‐seq, Crinier et al. provide conserved tissue‐specific gene signatures of NK cells from spleen and blood and identified two major NK cell subsets transcriptionally similar across organs and species.
Journal ArticleDOI
Innate lymphoid cells: major players in inflammatory diseases.
TL;DR: The roles of ILCs in inflammatory diseases are detailed; this work covers type 2 inflammatory diseases (such as asthma, chronic rhinosinusitis and atopic dermatitis), as well as inflammatory bowel diseases, psoriasis and other systemic or organ-specific inflammatory and autoimmune diseases.
Journal ArticleDOI
Evidence of innate lymphoid cell redundancy in humans
Frédéric Vély,Vincent Barlogis,Blandine Vallentin,Bénédicte Neven,Christelle Piperoglou,Mikael Ebbo,Thibaut Perchet,Thibaut Perchet,Maxime Petit,Maxime Petit,Nadia Yessaad,Fabien Touzot,Fabien Touzot,Julie Bruneau,Julie Bruneau,Nizar Mahlaoui,Nicolas Zucchini,Catherine Farnarier,Gérard Michel,Despina Moshous,Stéphane Blanche,Arnaud Dujardin,Hergen Spits,Jörg H W Distler,Andreas Ramming,Capucine Picard,Rachel Golub,Rachel Golub,Alain Fischer,Eric Vivier +29 more
TL;DR: The authors investigated the presence of ILCs in a cohort of patients with severe combined immunodeficiency (SCID) and found that ILC subsets were absent in patients with SCID who had mutation of the gene encoding the common γ-chain cytokine receptor subunit IL-2Rγ or the tyrosine kinase JAK3.
Journal ArticleDOI
IgG4-related systemic disease: features and treatment response in a French cohort: results of a multicenter registry.
Mikael Ebbo,Laurent Daniel,Michel Pavic,Pascal Sève,Mohamed Hamidou,Emmanuel Andrès,Stéphane Burtey,Laurent Chiche,Jacques Serratrice,Maïté Longy-Boursier,Marc Ruivard,Julien Haroche,Bertrand Godeau,Anne-Bérengère Beucher,Jean-Marie Berthelot,Thomas Papo,Jean-Loup Pennaforte,Audrey Benyamine,Noémie Jourde,Cédric Landron,Pascal Roblot,Olivier Moranne,Christine Silvain,Brigitte Granel,F. Bernard,Véronique Veit,Karin Mazodier,Emmanuelle Bernit,H. Rousset,José Boucraut,Jean-Jacques Boffa,Pierre-Jean Weiller,Gilles Kaplanski,Pierre Aucouturier,Jean-Robert Harlé,Nicolas Schleinitz +35 more
TL;DR: In this paper, the clinical, laboratory, and histologic characteristics of 25 patients from a French nationwide cohort were reported, which strongly suggest the implication of a T-cell dependent B-cell polyclonal activation in IgG4-related systemic disease, probably under the control of T helper follicular cells.