His main research concerns Immunology, Autoimmunity, Immunodeficiency, Autoimmune lymphoproliferative syndrome and Internal medicine. His Immunology research incorporates themes from Apoptosis, Disease and Fas receptor. He combines subjects such as Enteropathy, Autoimmune enteropathy, Lymphoproliferative disorders and IPEX syndrome with his study of Autoimmunity.
His research in Immunodeficiency intersects with topics in Genetic enhancement and Oncology. Frédéric Rieux-Laucat has included themes like Germline mutation and Lymphocyte in his Autoimmune lymphoproliferative syndrome study. The Internal medicine study combines topics in areas such as Nonsense mutation, Endocrinology and Severe combined immunodeficiency.
Frédéric Rieux-Laucat mainly focuses on Immunology, Autoimmune lymphoproliferative syndrome, Autoimmunity, Apoptosis and Cancer research. His Immunology study incorporates themes from Mutation, Germline mutation and Fas receptor. His work carried out in the field of Autoimmune lymphoproliferative syndrome brings together such families of science as Fas ligand, Somatic cell, Autoimmune disease, Germline and Lymphocyte homeostasis.
His Autoimmunity research is multidisciplinary, incorporating perspectives in Phenotype, T cell and CD8, Antigen. His Apoptosis research is multidisciplinary, relying on both Hypergammaglobulinemia, Cytotoxic T cell, Lymphoproliferative disorders and Cell biology. Frédéric Rieux-Laucat works mostly in the field of Immunodeficiency, limiting it down to topics relating to Internal medicine and, in certain cases, Endocrinology.
Frédéric Rieux-Laucat spends much of his time researching Immunology, Autoimmune lymphoproliferative syndrome, Interferon, Autoimmunity and Cancer research. His work on Immune system, Autoimmune disease and Evans syndrome is typically connected to Sting and Population as part of general Immunology study, connecting several disciplines of science. His studies in Autoimmune lymphoproliferative syndrome integrate themes in fields like Streptococcus pneumoniae, Immunodeficiency, Familial Mediterranean fever, Hepatosplenomegaly and MEFV.
His studies deal with areas such as Proinflammatory cytokine, Interleukin and Wild type as well as Interferon. The concepts of his Autoimmunity study are interwoven with issues in Acquired immune system and T cell. His Cancer research study which covers Gene that intersects with Lymphoma and Fas receptor.
His scientific interests lie mostly in Immunology, Interferon, Autoimmune disease, T cell and Disease. His Immunology study typically links adjacent topics like Genetic determinism. His work on Alpha interferon as part of general Interferon research is frequently linked to Sting, bridging the gap between disciplines.
His Autoimmune disease study incorporates themes from Mutation, Germline mutation, Autoimmune hemolytic anemia, Evans syndrome and LRBA. His T cell research integrates issues from Acquired immune system, Antigen, Autoimmune lymphoproliferative syndrome and B-cell receptor. His Disease research focuses on Autoantibody and how it connects with Asymptomatic, Phenocopy, Immunity and Case-control study.
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Impaired type I interferon activity and inflammatory responses in severe COVID-19 patients.
Jérôme Hadjadj;Nader Yatim;Laura Barnabei;Aurélien Corneau.
Mutations in Fas associated with human lymphoproliferative syndrome and autoimmunity
F. Rieux-Laucat;F. Le Deist;C. Hivroz;I. A. G. Roberts.
Autoantibodies against type I IFNs in patients with life-threatening COVID-19.
Paul Bastard;Paul Bastard;Paul Bastard;Lindsey B. Rosen;Qian Zhang;Eleftherios Michailidis.
XIAP deficiency in humans causes an X-linked lymphoproliferative syndrome
Stéphanie Rigaud;Marie-Claude Fondanèche;Nathalie Lambert;Nathalie Lambert;Benoit Pasquier.
Efficacy of Gene Therapy for X-Linked Severe Combined Immunodeficiency
Salima Hacein-Bey-Abina;Julia Hauer;Annick Lim;Capucine Picard.
The New England Journal of Medicine (2010)
STIM1 Mutation Associated with a Syndrome of Immunodeficiency and Autoimmunity
Capucine Picard;Christie Ann McCarl;Alexander Papolos;Sara Khalil.
The New England Journal of Medicine (2009)
Revised diagnostic criteria and classification for the autoimmune lymphoproliferative syndrome (ALPS): report from the 2009 NIH International Workshop.
Joao B. Oliveira;Jack J. Bleesing;Umberto Dianzani;Thomas A. Fleisher.
Inherited STING-activating mutation underlies a familial inflammatory syndrome with lupus-like manifestations
Nadia Jeremiah;Bénédicte Neven;Matteo Gentili;Isabelle Callebaut.
Journal of Clinical Investigation (2014)
Autoimmune Lymphoproliferative Syndrome with Somatic Fas Mutations
Eliska Holzelova;Cédric Vonarbourg;Marie Claude Stolzenberg;Peter D. Arkwright.
The New England Journal of Medicine (2004)
Severe Food Allergy as a Variant of IPEX Syndrome Caused by a Deletion in a Noncoding Region of the FOXP3 Gene
Troy R Torgerson;Avriel Linane;Nicolette Moes;Stephanie Anover.
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