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26 results on '"Fayand, Antoine"'

1. FLT3L governs the development of partially overlapping hematopoietic lineages in humans and mice

Author

Momenilandi, Mana, Lévy, Romain, Sobrino, Steicy, Li, Jingwei, Lagresle-Peyrou, Chantal, Esmaeilzadeh, Hossein, Fayand, Antoine, Le Floc’h, Corentin, Guérin, Antoine, Della Mina, Erika, Shearer, Debra, Delmonte, Ottavia M., Yatim, Ahmad, Mulder, Kevin, Mancini, Mathieu, Rinchai, Darawan, Denis, Adeline, Neehus, Anna-Lena, Balogh, Karla, Brendle, Sarah, Rokni-Zadeh, Hassan, Changi-Ashtiani, Majid, Seeleuthner, Yoann, Deswarte, Caroline, Bessot, Boris, Cremades, Cassandre, Materna, Marie, Cederholm, Axel, Ogishi, Masato, Philippot, Quentin, Beganovic, Omer, Ackermann, Mania, Wuyts, Margareta, Khan, Taushif, Fouéré, Sébastien, Herms, Florian, Chanal, Johan, Palterer, Boaz, Bruneau, Julie, Molina, Thierry J., Leclerc-Mercier, Stéphanie, Prétet, Jean-Luc, Youssefian, Leila, Vahidnezhad, Hassan, Parvaneh, Nima, Claeys, Kristl G., Schrijvers, Rik, Luka, Marine, Pérot, Philippe, Fourgeaud, Jacques, Nourrisson, Céline, Poirier, Philippe, Jouanguy, Emmanuelle, Boisson-Dupuis, Stéphanie, Bustamante, Jacinta, Notarangelo, Luigi D., Christensen, Neil, Landegren, Nils, Abel, Laurent, Marr, Nico, Six, Emmanuelle, Langlais, David, Waterboer, Tim, Ginhoux, Florent, Ma, Cindy S., Tangye, Stuart G., Meyts, Isabelle, Lachmann, Nico, Hu, Jiafen, Shahrooei, Mohammad, Bossuyt, Xavier, Casanova, Jean-Laurent, and Béziat, Vivien

Published
2024
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4. Pathogenic variants in the NLRP3 LRR domain at position 861 are responsible for a boost-dependent atypical CAPS phenotype

Author

Fayand, Antoine, Cescato, Margaux, Le Corre, Laurent, Terré, Alexandre, Wacheux, Margaux, Zhu, Yixiang Y.J., Melet, Armelle, Moreau, Thomas R.J., Bodaghi, Bahram, Bonnet, Fabrice, Bronnimann, Didier, Cuisset, Laurence, Faria, Raquel, Grateau, Gilles, Pillet, Pascal, Mulders-Manders, Catharina M., Neven, Benedicte, Quartier, Pierre, Richer, Olivier, Savey, Léa, Truchetet, Marie-Elise, Py, Bénédicte F., Boursier, Guilaine, Herbeuval, Jean-Philippe, Georgin-Lavialle, Sophie, and Rodero, Mathieu P.

Published
2023
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5. Successful treatment of JAK1-associated inflammatory disease

Author

Fayand, Antoine, Hentgen, Véronique, Posseme, Céline, Lacout, Carole, Picard, Capucine, Moguelet, Philippe, Cescato, Margaux, Sbeih, Nabiha, Moreau, Thomas R.J., Zhu, Yixiang Y.J., Charuel, Jean-Luc, Corneau, Aurélien, Deibener-Kaminsky, Joelle, Dupuy, Stéphanie, Fusaro, Mathieu, Hoareau, Benedicte, Hovnanian, Alain, Langlois, Vincent, Le Corre, Laurent, Maciel, Thiago T., Miskinyte, Snaigune, Miyara, Makoto, Moulinet, Thomas, Perret, Magali, Schuhmacher, Marie Hélène, Rignault-Bricard, Rachel, Viel, Sébastien, Vinit, Angélique, Soria, Angèle, Duffy, Darragh, Launay, Jean-Marie, Callebert, Jacques, Herbeuval, Jean Philippe, Rodero, Mathieu P., and Georgin-Lavialle, Sophie

Published
2023
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7. Diagnostic and therapeutic algorithms for monogenic autoinflammatory diseases presenting with recurrent fevers among adults.

Author

Delplanque, Marion, Fayand, Antoine, Boursier, Guilaine, Grateau, Gilles, Savey, Léa, and Georgin-Lavialle, Sophie

Subjects
*NATURAL immunity, *AUTOANTIBODIES, *FEVER, *GENETIC mutation, *CRYOPYRIN-associated periodic syndromes, *TUMOR necrosis factor receptor-associated periodic syndrome, *IMMUNE system, *GENETIC testing, *AUTOIMMUNE diseases, *DISEASE relapse, *MEVALONATE kinase deficiency, *AUTOINFLAMMATORY diseases, *ALGORITHMS, *ADULTS
Abstract

Autoinflammatory diseases (AIDs) are defined as disorders of innate immunity. They were initially defined in contrast to autoimmune diseases because of the lack of involvement of the adaptive immune system and circulating autoantibodies. The four monogenic AIDs first described are called the 'historical' AIDs and include FMF (associated with MEFV mutations), cryopyrinopathies (associated with NLRP3 mutations), TNF receptor–associated periodic syndrome (associated with TNFRSF1A mutations) and mevalonate kinase deficiency (MKD; associated with MVK mutations). In the last 10 years, >50 new monogenic AIDs have been discovered due to genetic advances. The most important discovery for adult patients is VEXAS syndrome associated with somatic UBA1 mutations leading to an AID affecting mostly elderly men. Diagnosis of monogenic AIDs is based on personal and family history and detailed analysis of symptoms associated with febrile attacks in the context of elevated peripheral inflammatory markers. This review proposes a practical approach for the diagnosis of the main monogenic AIDs among adult patients. [ABSTRACT FROM AUTHOR]

Published
2023
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9. Delayed Diagnosis of Chronic Necrotizing Granulomatous Skin Lesions due to TAP2 Deficiency

Author

Darazam, Ilad Alavi, primary, Hakamifard, Atousa, additional, Momenilandi, Mana, additional, Materna, Marie, additional, Gharehbagh, Farid Javandoust, additional, Shahrooei, Mohammad, additional, Olyaei, Nasrin Alipour, additional, Zerehpoosh, Farahnaz Bidari, additional, Fayand, Antoine, additional, Hatami, Firouze, additional, Lotfollahi, Legha, additional, Mansouri, Nahal, additional, Casanova, Jean-Laurent, additional, Béziat, Vivien, additional, and Mansouri, Davood, additional

Published
2022
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11. DADA2 diagnosed in adulthood versus childhood: A comparative study on 306 patients including a systematic literature review and 12 French cases

Author

Fayand, Antoine, primary, Chasset, François, additional, Boutboul, David, additional, Queyrel, Viviane, additional, Tieulié, Nathalie, additional, Guichard, Isabelle, additional, Dupin, Nicolas, additional, Franck, Nathalie, additional, Cohen, Pascal, additional, Bessis, Didier, additional, Guenno, Guillaume Le, additional, Koné-Paut, Isabelle, additional, Belot, Alexandre, additional, Bonhomme, Axelle, additional, Ducharme-Bénard, Stéphanie, additional, Grateau, Gilles, additional, Sarrabay, Guillaume, additional, Touitou, Isabelle, additional, Boursier, Guilaine, additional, and Georgin-Lavialle, Sophie, additional

Published
2021
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13. Onset and Relapse of Juvenile Dermatomyositis Following Asymptomatic SARS-CoV-2 Infection

Author

Rodero, Mathieu Paul, Pelleau, Stéphane, Welfringer-Morin, Anne, Duffy, Darragh, Melki, Isabelle, Bader-Meunier, Brigitte, Bondet, Vincent, Gitiaux, Cyril, Bonigen, Julie, Fayand, Antoine, Courdavault Vagh Weinmann, Laurence, Mahe, Emmanuel, Charuel, Jean Luc, Alyanakian, Marie-Alexandra, Herbeuval, Jean Philippe, White, Michael, Rodero, Mathieu, Évaluer l'immunité contre SARS-CoV-2 à l'échelle de la population grâce aux tests sérologiques - - CorPopImm2020 - ANR-20-COVI-0052 - COVID-19 - VALID, Variation de la réponse immune systémique et muqueuse pendant l'infection par le SRAS-CoV-2 et la convalescence - - CoVarImm2020 - ANR-20-COVI-0053 - COVID-19 - VALID, Laboratoire de Chimie et de Biochimie Pharmacologiques et Toxicologiques (LCBPT - UMR 8601), Institut de Chimie du CNRS (INC)-Centre National de la Recherche Scientifique (CNRS)-Université Paris Cité (UPCité), Epidémiologie et Analyse des Maladies Infectieuses - Infectious Disease Epidemiology and Analytics, Institut Pasteur [Paris] (IP)-Université Paris Cité (UPCité), CHU Necker - Enfants Malades [AP-HP], Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP), Immunologie Translationnelle - Translational Immunology lab, Laboratory of neurogenetics and neuroinflammation (Equipe Inserm U1163), Imagine - Institut des maladies génétiques (IHU) (Imagine - U1163), Institut National de la Santé et de la Recherche Médicale (INSERM)-Université Paris Cité (UPCité)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Université Paris Cité (UPCité), Centre de référence des rhumatismes inflammatoires et maladies autoimmunes systémiques rares de l'enfant [Paris] (RAISE), AP-HP Hôpital universitaire Robert-Debré [Paris], Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP), Service d'immuno-hématologie pédiatrique [CHU Necker], Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-CHU Necker - Enfants Malades [AP-HP], Immunogenetics of pediatric autoimmune diseases (Equipe Inserm U1163), Service de Médecine Interne = Hôpital de jour de médecine [CHU Tenon], CHU Tenon [AP-HP], Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Sorbonne Université (SU)-Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Sorbonne Université (SU), Centre Hospitalier Victor Dupouy, CHU Pitié-Salpêtrière [AP-HP], Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Sorbonne Université (SU), DD was supported by the Agence Nationale de la Recherche as part of the Flash Covid funding (CoVarImm). MW was supported by the Agence Nationale de la Recherche and Fondation pour la Recherche Médicale (CorPopImm)., FJDM study group, ANR-20-COVI-0052,CorPopImm,Évaluer l'immunité contre SARS-CoV-2 à l'échelle de la population grâce aux tests sérologiques(2020), ANR-20-COVI-0053,CoVarImm,Variation de la réponse immune systémique et muqueuse pendant l'infection par le SRAS-CoV-2 et la convalescence(2020), Institut de Chimie du CNRS (INC)-Centre National de la Recherche Scientifique (CNRS)-Université de Paris (UP), Institut Pasteur [Paris], Institut National de la Santé et de la Recherche Médicale (INSERM)-Université de Paris (UP)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Université de Paris (UP), Service de Médecine Interne [CHU Tenon], Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-CHU Tenon [AP-HP], Sorbonne Université (SU)-Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Sorbonne Université (SU), Institut National de la Santé et de la Recherche Médicale (INSERM)-Université Paris Cité (UPCité), Hôpital Robert Debré, and FJDM Study group Vincent Bondet, Cyril Gitiaux, Julie Bonigen, Antoine Fayand, Laurence Courdavault Vagh Weinmann, Emmanuel Mahe, Jean Luc Charuel, Marie-Alexandra Alyanakian, Jean Philippe Herbeuva, Michael White

Subjects
030203 arthritis & rheumatology, 0303 health sciences, medicine.medical_specialty, 2019-20 coronavirus outbreak, Coronavirus disease 2019 (COVID-19), business.industry, Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), [SDV]Life Sciences [q-bio], Immunology, medicine.disease, Letter to Editor, Virology, Asymptomatic, 3. Good health, [SDV] Life Sciences [q-bio], 03 medical and health sciences, 0302 clinical medicine, Medical microbiology, Immunology and Allergy, Medicine, medicine.symptom, business, Juvenile dermatomyositis, ComputingMilieux_MISCELLANEOUS, 030304 developmental biology
Abstract

International audience; No abstract available

Published
2021

15. Clinical and pathological dermatological features of deficiency of adenosine deaminase 2: A multicenter, retrospective, observational study

Author

Chasset, François, primary, Fayand, Antoine, additional, Moguelet, Philippe, additional, Kouby, Floriane, additional, Bonhomme, Axelle, additional, Franck, Nathalie, additional, Goldman-lévy, Gabrielle, additional, Fraitag, Sylvie, additional, Barbaud, Annick, additional, Queyrel, Viviane, additional, Touitou, Isabelle, additional, Boursier, Guilaine, additional, Sarrabay, Guillaume, additional, Ducharme-Benard, Stéphanie, additional, Dupin, Nicolas, additional, Francès, Camille, additional, Bessis, Didier, additional, and Georgin-Lavialle, Sophie, additional

Published
2020
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17. A meal served cold

Author

Fayand, Antoine, primary, Barreau, Sylvain, additional, Terrier, Benjamin, additional, and Chapuis, Nicolas, additional

Published
2020
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20. Epidemiology of Castleman disease associated with AA amyloidosis: description of 2 new cases and literature review

Author

Fayand, Antoine, primary, Boutboul, David, additional, Galicier, Lionel, additional, Kahn, Jean-Emmanuel, additional, Buob, David, additional, Boffa, Jean-Jacques, additional, Cez, Alexandre, additional, Oksenhendler, Eric, additional, Grateau, Gilles, additional, Ducharme-Bénard, Stéphanie, additional, and Georgin-Lavialle, Sophie, additional

Published
2019
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21. Onset and Relapse of Juvenile Dermatomyositis Following Asymptomatic SARS-CoV-2 Infection.

Author

Rodero, Mathieu Paul, Pelleau, Stéphane, Welfringer-Morin, Anne, Duffy, Darragh, Melki, Isabelle, Bader-Meunier, Brigitte, FJDM Study group, Bondet, Vincent, Gitiaux, Cyril, Bonigen, Julie, Fayand, Antoine, Weinmann, Laurence Courdavault Vagh, Mahe, Emmanuel, Charuel, Jean Luc, Alyanakian, Marie-Alexandra, Herbeuva, Jean Philippe, and White, Michael

Subjects
JUVENILE diseases, SARS-CoV-2, DERMATOMYOSITIS, INFECTION, NEUROMUSCULAR diseases
Abstract

Dear Editor, SARS-CoV-2 infection drives a marked inflammation and has been described to precede the appearance in rare occasion of various autoimmune and inflammatory diseases including clinical, radiological, muscle biopsy, and serological features consistent with dermatomyositis [[1]]. Altogether, out of the 10 patients with onset or relapse of JDM features seen in our center between April 2020 and March 2021, we identified 2 (20%) with a concomitant history of SARS-CoV-2 infection. [Extracted from the article]

Published
2022
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22. Massive Splenomegaly Indicating Sarcoidosis

Author

Bachmeyer, Claude, primary, Fayand, Antoine, additional, Georgin-Lavialle, Sophie, additional, Fedida, Benjamin, additional, Naccache, Jean-Marc, additional, Lionnet, François, additional, and Amiot, Xavier, additional

Published
2017
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25. Correction to: Onset and Relapse of Juvenile Dermatomyositis Following Asymptomatic SARS-CoV-2 Infection.

Author

Rodero, Mathieu Paul, Pelleau, Stéphane, Welfringer-Morin, Anne, FJDM study group, Bondet, Vincent, Gitiaux, Cyril, Bonigen, Julie, Fayand, Antoine, Weinmann, Laurence Courdavault Vagh, Mahe, Emmanuel, Charuel, Jean Luc, Alyanakian, Marie-Alexandra, Herbeuval, Jean Philippe, White, Michael, Duffy, Darragh, Melki, Isabelle, and Bader-Meunier, Brigitte

Subjects
JUVENILE diseases, SARS-CoV-2, NEUROMUSCULAR diseases
Published
2022
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26. Malignant Peritoneal Mesothelioma Complicating Familial Mediterranean Fever on 18 F-FDG PET/CT.

Author

Fayand A, Kerrou K, Wendum D, Grateau G, and Georgin-Lavialle S

Subjects
Male, Humans, Aged, Positron Emission Tomography Computed Tomography, Fluorodeoxyglucose F18, Familial Mediterranean Fever complications, Familial Mediterranean Fever diagnostic imaging, Familial Mediterranean Fever drug therapy, Mesothelioma complications, Mesothelioma diagnostic imaging, Mesothelioma, Malignant complications, Peritoneal Neoplasms complications, Peritoneal Neoplasms diagnostic imaging, Peritoneal Neoplasms pathology
Abstract

Abstract: A 77-year-old man with a personal history of familial Mediterranean fever presented with a slowly enlarging tumefaction of the left abdominal wall and persistent inflammatory syndrome despite good adherence to colchicine. 18 F-FDG PET/CT showed a hypermetabolic muscular mass of the abdominal wall along with other hypermetabolic lesions including a peritoneal mass and several subcutaneous soft tissue nodules. CT-guided needle biopsy led to the diagnosis of a muscular localization of a malignant peritoneal mesothelioma, which is an extremely rare complication of familial Mediterranean fever. Six courses of chemotherapy with carboplatin and pemetrexed allowed an almost complete response., Competing Interests: Conflicts of interest and sources of funding: none declared., (Copyright © 2024 Wolters Kluwer Health, Inc. All rights reserved.)

Published
2024
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