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208 results on '"Nicaise-Roland, Pascale"'

5. Arterial Thrombotic Events in Adult Inpatients With COVID-19

Author

Fournier, Morgane, Faille, Dorothée, Dossier, Antoine, Mageau, Arthur, Nicaise Roland, Pascale, Ajzenberg, Nadine, Borie, Raphael, Bouadma, Lila, Bunel, Vincent, Castier, Yves, Choquet, Christophe, Crestani, Bruno, Daugas, Eric, Deconinck, Laurene, Descamps, Diane, Descamps, Vincent, Dieudé, Philippe, Ducrocq, Gregory, Faucher, Nathalie, Goulenok, Tiphaine, Guidoux, Céline, Khalil, Antoine, Lavallée, Philippa, Lescure, François Xavier, Lortat-Jacob, Brice, Mal, Hervé, Mutuon, Pierre, Pellenc, Quentin, Steg, Philippe Gabriel, Taille, Camille, Timsit, Jean Francois, Yazdanpanah, Yazdan, Papo, Thomas, and Sacré, Karim

Published
2021
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6. Rocuronium-specific antibodies drive perioperative anaphylaxis but can also function as reversal agents in preclinical models.

Author

Dejoux, Alice, Zhu, Qianqian, Ganneau, Christelle, Goff, Odile Richard-Le, Godon, Ophélie, Lemaitre, Julien, Relouzat, Francis, Huetz, François, Sokal, Aurélien, Vandenberghe, Alexis, Pecalvel, Cyprien, Hunault, Lise, Derenne, Thomas, Gillis, Caitlin M., Iannascoli, Bruno, Wang, Yidan, Rose, Thierry, Mertens, Christel, Nicaise-Roland, Pascale, and England, Patrick

Subjects
IMMUNOGLOBULIN E, IMMUNOLOGIC memory, NEUROMUSCULAR blocking agents, NEUROMUSCULAR blockade, MAST cells
Abstract

Neuromuscular blocking agents (NMBAs) relax skeletal muscles to facilitate surgeries and ease intubation but can lead to adverse reactions, including complications because of postoperative residual neuromuscular blockade (rNMB) and, in rare cases, anaphylaxis. Both adverse reactions vary between types of NMBAs, with rocuronium, a widely used nondepolarizing NMBA, inducing one of the longest rNMB durations and highest anaphylaxis incidences. rNMB induced by rocuronium can be reversed by the synthetic γ-cyclodextrin sugammadex. However, in rare cases, sugammadex can provoke anaphylaxis. Thus, additional therapeutic options are needed. Rocuronium-induced anaphylaxis is proposed to rely on preexisting rocuronium-binding antibodies. To understand the pathogenesis of rocuronium-induced anaphylaxis and to identify potential therapeutics, we investigated the memory B cell antibody repertoire of patients with suspected hypersensitivity to rocuronium. We identified polyclonal antibody repertoires with a high diversity among V(D)J genes without evidence of clonal groups. When recombinantly expressed, these antibodies demonstrated specificity and low affinity for rocuronium without cross-reactivity for other NMBAs. Moreover, when these antibodies were expressed as human immunoglobulin E (IgE), they triggered human mast cell activation and passive systemic anaphylaxis in transgenic mice, although their affinities were insufficient to serve as reversal agents. Rocuronium-specific, high-affinity antibodies were thus isolated from rocuronium-immunized mice. The highest-affinity antibody was able to reverse rocuronium-induced neuromuscular blockade in nonhuman primates with kinetics comparable to that of sugammadex. Together, these data support the hypothesis that antibodies cause anaphylactic reactions to rocuronium and pave the way for improved diagnostics and neuromuscular blockade reversal agents. Editor's summary: Neuromuscular blocking agents (NMBAs) such as rocuronium are used during anesthesia to assist with surgeries and intubations. Although these agents are effective, they are not without risk. Patients can develop postoperative residual neuromuscular blockade, which can be treated with an NMBA reversal agent, and life-threatening anaphylaxis can occur in rare cases. Here, Dejoux et al. isolated and characterized memory B cells from three individuals who developed reactions to NMBA treatment and had serum antibodies to rocuronium. The authors found that IgE antibodies generated from these memory B cells were sufficient to induce anaphylaxis in mice treated with rocuronium, although they were too low affinity to be used as reversal agents. This led the authors to immunize mice with rocuronium to generate antibodies of higher affinity, which were able to reverse neuromuscular blockade in rocuronium-treated nonhuman primates. Together, these data explain why these three patients had a reaction and offer a therapeutic approach to reversing neuromuscular blockade. —Courtney Malo [ABSTRACT FROM AUTHOR]

Published
2024
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8. Refractory obstetrical antiphospholipid syndrome: Features, treatment and outcome in a European multicenter retrospective study

Author

Mekinian, Arsène, Alijotas-Reig, Jaume, Carrat, Fabrice, Costedoat-Chalumeau, Nathalie, Ruffatti, Amelia, Lazzaroni, Maria Grazia, Tabacco, Sara, Maina, Aldo, Masseau, Agathe, Morel, Nathalie, Esteve-Valverde, Enrique Esteve, Ferrer-Oliveras, Raquel, Andreoli, Laura, De Carolis, Sara, Josselin-Mahr, Laurence, Abisror, Noémie, Nicaise-Roland, Pascale, Tincani, Angela, and Fain, Olivier

Published
2017
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10. Risk stratification through extensive allergy work‐up in COVID‐19‐mRNA vaccine allergic reactions

Author

Soria, Angèle, primary, Labella, Marina, additional, Doña, Inmaculada, additional, Nicaise‐Roland, Pascale, additional, Chollet‐Martin, Sylvie, additional, Autegarden, Jean‐Eric, additional, Castagna, Julie, additional, Le Thai, Claire, additional, de Chaisemartin, Luc, additional, Torres, Maria José, additional, and Barbaud, Annick, additional

Published
2023
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11. The efficacy of hydroxychloroquine for obstetrical outcome in anti-phospholipid syndrome: Data from a European multicenter retrospective study

Author

Mekinian, Arsène, Lazzaroni, Maria Grazia, Kuzenko, Anna, Alijotas-Reig, Jaume, Ruffatti, Amelia, Levy, Pierre, Canti, Valentina, Bremme, Katarina, Bezanahary, Holy, Bertero, Tiziana, Dhote, Robin, Maurier, Francois, Andreoli, Laura, Benbara, Amélie, Tigazin, Ahmed, Carbillon, Lionel, Nicaise-Roland, Pascale, Tincani, Angela, and Fain, Olivier

Published
2015
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20. Netherton syndrome subtypes share IL-17/IL-36 signature with distinct IFN-α and allergic responses

Author

Barbieux, Claire, Bonnet Des Claustres, Mathilde, Fahrner, Matthias, Petrova, Evgeniya, Tsoi, Lam, Gouin, Olivier, Leturcq, Florent, Nicaise-Roland, Pascale, Bole, Christine, Béziat, Vivien, Bourrat, Emmanuelle, Schilling, Oliver, Gudjonsson, Johann, Hovnanian, Alain, Genetic skin diseases : from disease mechanism to therapies (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), University of Freiburg [Freiburg], Department of Biology [Fribourg], Institut National de la Santé et de la Recherche Médicale (INSERM), Unité Fonctionnelles d′Immunologie [CHU Bichat], Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-AP-HP - Hôpital Bichat - Claude Bernard [Paris], Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP), Institut National de la Santé et de la Recherche Médicale (INSERM)-Université Paris Cité (UPCité), Human genetics of infectious diseases : Mendelian predisposition (Equipe Inserm U1163), Service de Dermatologie [AP-HP Hôpital Saint-Louis], Hopital Saint-Louis [AP-HP] (AP-HP), Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP), University of Michigan [Ann Arbor], University of Michigan System, Université Paris Cité (UPCité), Service de Génétique Médicale [CHU Necker], Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-CHU Necker - Enfants Malades [AP-HP], This project was funded by the French National Research Agency ANR-17-CE14-0025 Tfh Atopy (A.H.), ANR-19-CE17-0017 Target-NS (A.H.), the Imagine Institute with Cross-Lab program, and Association Ichtyose France (A.H.). A.H. and O.S. were supported by the European Union’s Horizon 2020 research and innovation program under the ERA-NET Cofund action 643578 (KLKIN project), J.E.G. and L.C.T. are supported by NIH P30-AR075043 and AI130025., ANR-17-CE14-0025,Tfh-Atopy,Différentiation et rôle pathogénique des lymphocytes T auxiliaires folliculaires dans la marche atopique(2017), ANR-19-CE17-0017,TARGET-NS,Développement d'une nouvelle biothérapie ciblant les mécanismes inflammatoires du syndrome de Netherton(2019), European Project: 643578,H2020,H2020-HCO-2014,E-Rare-3(2014), Université Paris Cité, Equipe HAL, Différentiation et rôle pathogénique des lymphocytes T auxiliaires folliculaires dans la marche atopique - - Tfh-Atopy2017 - ANR-17-CE14-0025 - AAPG2017 - VALID, Développement d'une nouvelle biothérapie ciblant les mécanismes inflammatoires du syndrome de Netherton - - TARGET-NS2019 - ANR-19-CE17-0017 - AAPG2019 - VALID, and ERA-NET rare disease research implementing IRDiRC objectives - E-Rare-3 - - H20202014-12-01 - 2019-11-30 - 643578 - VALID

Subjects
TH2, IL-36, scaly erythroderma, [SDV.IMM] Life Sciences [q-bio]/Immunology, integumentary system, ichthyosis linearis circumflexa, TH9, [SDV.IMM]Life Sciences [q-bio]/Immunology, Netherton syndrome, type I IFN
Abstract

International audience; Background: Netherton syndrome (NS) is a rare recessive skin disorder caused by loss-of-function mutations in SPINK5 encoding the protease inhibitor LEKTI (lymphoepithelial Kazal-type–related inhibitor). NS patients experience severe skin barrier defects, display inflammatory skin lesions, and have superficial scaling with atopic manifestations. They present with typical ichthyosis linearis circumflexa (NS-ILC) or scaly erythroderma (NS-SE). Objective: We used a combination of several molecular profiling methods to comprehensively characterize the skin, immune cells, and allergic phenotypes of NS-ILC and NS-SE patients. Methods: We studied a cohort of 13 patients comprising 9 NS-ILC and 4 NS-SE. Results: Integrated multiomics revealed abnormal epidermal proliferation and differentiation and IL-17/IL-36 signatures in lesion skin and in blood in both NS endotypes. Although the molecular profiles of NS-ILC and NS-SE lesion skin were very similar, nonlesion skin of each disease subtype displayed distinctive molecular features. Nonlesion and lesion NS-SE epidermis showed activation of the type I IFN signaling pathway, while lesion NS-ILC skin differed from nonlesion NS-ILC skin by increased complement activation and neutrophil infiltration. Serum cytokine profiling and immunophenotyping of circulating lymphocytes showed a TH2-driven allergic response in NS-ILC, whereas NS-SE patients displayed mainly a TH9 axis with increased CCL22/MDC and CCL17/TARC serum levels. Conclusions: This study confirms IL-17/IL-36 as the predominant signaling axes in both NS endotypes and unveils molecular features distinguishing NS-ILC and NS-SE. These results identify new therapeutic targets and could pave the way for precision medicine of NS.

Published
2021
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30. Obstetrical outcome and treatments in seronegative primary APS : data from European retrospective study

Author

Abisror, Noemie, Nguyen, Yann, Marozio, Luca, Esteve Valverde, Enrique, Udry, Sebastian, Pleguezuelo, Daniel Enrique, Billoir, Paul, Mayer-Pickel, Karoline, Urbanski, Geoffrey, Zigon, Polona, De Moreuil, Claire, Hoxha, Ariela, Bezanahary, Holy, Carbillon, Lionel, Kayem, Gilles, Bornes, Marie, Yelnik, Cecile, Johanet, Cathererine, Nicaise-Roland, Pascale, Lambert, Marc, Salle, Valéry, Latino, Omar Jose, Hachulla, Eric, Benedetto, Chiara, Bourrienne, Marie Charlotte, Benhamou, Ygal, Alijotas-Reig, Jaume, Fain, Olivier, Mekinian, Arsène, Abisror, Noemie, Nguyen, Yann, Marozio, Luca, Esteve Valverde, Enrique, Udry, Sebastian, Pleguezuelo, Daniel Enrique, Billoir, Paul, Mayer-Pickel, Karoline, Urbanski, Geoffrey, Zigon, Polona, De Moreuil, Claire, Hoxha, Ariela, Bezanahary, Holy, Carbillon, Lionel, Kayem, Gilles, Bornes, Marie, Yelnik, Cecile, Johanet, Cathererine, Nicaise-Roland, Pascale, Lambert, Marc, Salle, Valéry, Latino, Omar Jose, Hachulla, Eric, Benedetto, Chiara, Bourrienne, Marie Charlotte, Benhamou, Ygal, Alijotas-Reig, Jaume, Fain, Olivier, and Mekinian, Arsène

Abstract

To compare characteristics, pregnancies and treatments during pregnancies of seronegative and seropositive antiphospholipid syndrome (APS), to analyse factors associated with obstetrical outcome. Inclusion criteria were: (1) thrombotic and/or obstetrical APS (Sydney criteria); (2) absence of conventional antiphospholipid antibodies (APL); (3) at least one persistent non-conventional APL among IgA anticardiolipin antibodies, IgA anti-B2GPI, anti-vimentin G/M, anti-annexin V G/M, anti-phosphatidylethanolamine G/M and anti-phosphatidylserine/prothrombin G/M antibodies. The exclusion criteria were: (1) systemic lupus erythematosus (SLE) or SLE-like disease; and (2) other connective tissue disease. A total of 187 women (mean 33±5 years) with seronegative APS were included from 14 centres in Austria, Spain, Italy, Slovenia and France and compared with 285 patients with seropositive APS. Seronegative APS has more obstetrical rather than thrombotic phenotypes, with only 6% of venous thrombosis in comparison to seropositive APS. Cumulative incidence of adverse obstetrical events was similar in seronegative and seropositive APS patients, although higher rates of intrauterine deaths (15% vs 5%; p=0.03), of preeclampsia (7% vs 16%, p=0.048) and lower live birth term (36±3 vs 38±3 weeks of gestation; p=0.04) were noted in seropositive APS. The cumulative incidence of adverse obstetrical events was significantly improved in treated versus untreated seronegative APS (log rank<0.05), whereas there was no difference between patients who received aspirin or aspirin-low-molecular weighted heparin combination. Several non-criteria APL can be detected in patients with clinical APS features without any conventional APL, with various rates. The detection of non-criteria APL and thus the diagnosis of seronegative APS could discuss the therapeutic management similar to seropositive APS, but well-designed controlled studies are necessary

Published
2020

34. European registry of babies born to mothers with antiphospholipid syndrome

Author

Mekinian, Arsene, Lachassinne, Eric, Nicaise-Roland, Pascale, Carbillon, Lionel, Motta, Mario, Vicaut, Eric, Boinot, Catherine, Avcin, Tadej, Letoumelin, Philippe, De Carolis, Sara, Rovere-Querini, Patrizia, Lambert, Marc, Derenne, Sophie, Pourrat, Olivier, Stirnemann, Jerome, Chollet-Martin, Sylvie, Biasini-Rebaioli, Chiara, Rovelli, Rosanna, Lojacono, Andrea, Ambrozic, Ales, Botta, Angela, Benbara, Amelie, Pierre, Fabrice, Allegri, Flavio, Nuzzo, Monica, Hatron, Pierre-Yves, Tincani, Angela, Fain, Olivier, Aurousseau, Marie-Helene, and Boffa, Marie-Claire

Published
2013
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36. Performance criteria for the verification of IgE and tryptase assay methods: recommendations from the AllergoBioNet network

Author

Sarrat, Anne, additional, Couderc, Rémy, additional, Alyanakian, Marie-Alexandra, additional, Apoil, Pol-André, additional, Beauvillain, Céline, additional, Chollet, Lionel, additional, Chrétien, Pascale, additional, Cirée, Arnaud, additional, Cypriani, Benoît, additional, Dumontet, Erwan, additional, Evrard, Bertrand, additional, Garnier, Lorna, additional, Grenier, Angélique, additional, Guérin, Valérie, additional, Hémont, Caroline, additional, Léon, Anthony, additional, Mariotte, Delphine, additional, Nicaise-Roland, Pascale, additional, Pernollet, Martine, additional, Rogeau, Stéphanie, additional, Tabary, Thierry, additional, Uring-Lambert, Béatrice, additional, Vivinus, Mylène, additional, and Vitte, Joana, additional

Published
2020
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39. An IgG-induced neutrophil activation pathway contributes to human drug-induced anaphylaxis

Author

Jönsson, Friederike, primary, de Chaisemartin, Luc, additional, Granger, Vanessa, additional, Gouel-Chéron, Aurélie, additional, Gillis, Caitlin M., additional, Zhu, Qianqian, additional, Dib, Fadia, additional, Nicaise-Roland, Pascale, additional, Ganneau, Christelle, additional, Hurtado-Nedelec, Maria, additional, Paugam-Burtz, Catherine, additional, Necib, Skander, additional, Keita-Meyer, Hawa, additional, Le Dorze, Matthieu, additional, Cholley, Bernard, additional, Langeron, Olivier, additional, Jacob, Laurent, additional, Plaud, Benoit, additional, Fischler, Marc, additional, Sauvan, Caroline, additional, Guinnepain, Marie-Thérèse, additional, Montravers, Philippe, additional, Aubier, Michel, additional, Bay, Sylvie, additional, Neukirch, Catherine, additional, Tubach, Florence, additional, Longrois, Dan, additional, Chollet-Martin, Sylvie, additional, and Bruhns, Pierre, additional

Published
2019
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41. Critères de performance pour la vérification des méthodes de dosages des IgE et de la tryptase : recommandations du réseau AllergoBioNet.

Author

Sarrat, Anne, Couderc, Rémy, Alyanakian, Marie-Alexandra, Apoil, Pol-André, Beauvillain, Céline, Chollet, Lionel, Chrétien, Pascale, Cirée, Arnaud, Cypriani, Benoît, Dumontet, Erwan, Evrard, Bertrand, Garnier, Lorna, Grenier, Angélique, Guérin, Valérie, Hémont, Caroline, Léon, Anthony, Mariotte, Delphine, Nicaise-Roland, Pascale, Pernollet, Martine, and Rogeau, Stéphanie

Published
2020
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43. Non-conventional antiphospholipid antibodies in patients with clinical obstetrical APS: prevalence and pregnancies treatment efficacy

Author

Mekinian, Arsène, Bourrienne, Marie-Charlotte, Carbillon, Lionel, Benbara, Amélie, Abisror, Noémie, Chollet-Martin, Sylvie, Tigaizin, Ahmed, Montestruc, Francois, Fain, Olivier, Nicaise-Roland, Pascale, Service de rhumatologie [CHU Saint-Antoine], CHU Saint-Antoine [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), Unité Fonctionnelles d′Immunologie [CHU Bichat], Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-AP-HP - Hôpital Bichat - Claude Bernard [Paris], Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP), Service de gynécologie-obstétrique [Hôpital Jean Verdier], Université Paris 13 (UP13)-Hôpital Jean Verdier [AP-HP], Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP), and eXYSTAT [Malakoff]

Subjects
obstetrical complications, [SDV.IMM]Life Sciences [q-bio]/Immunology, [SDV.MHEP.GEO]Life Sciences [q-bio]/Human health and pathology/Gynecology and obstetrics, non-conventional antiphospholipids, antiphospholipid syndrome, pregnancies treatment
Abstract

International audience; ObjectivesTo describe the prevalence of non-conventional APL in patients with obstetrical APS without conventional APL and the impact of treatment on pregnancy outcome.MethodsPatients with clinical obstetrical criteria were tested for anti-phosphatidylethanolamine (aPE) IgG/M, anti-prothrombin/phosphatidylserine (anti-PS/PT) IgG/M and anti-annexin V IgG. Pregnancies losses rates were compared between APS, non-conventional APS and non-APL and in untreated pregnancies to treated ones for each group.ResultsUsing the cut-offs (ROC), 65/96 (68%) patients have been considered as non-conventional APS and compared to 83 APS and 31 patients without APL. The obstetrical history in non-conventional APS did not differ in comparison to confirmed APS. The frequencies of anti-annexin V IgG antibodies tended to be more frequent in non-conventional APS (88% versus 73%; p=0.06), and those of anti-PE IgG and M were similar. The anti-PS/PT IgG and M antibodies were more frequent in confirmed APS than in non-conventional APS (63% and 37% versus 4% and 5%, p

Published
2016
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44. Predictive value of autoantibodies from anti-CCP2, anti-MCV and anti-human citrullinated fibrinogen tests, in early rheumatoid arthritis patients with rapid radiographic progression at 1 year: results from the ESPOIR cohort

Author

Degboé, Yannick, Constantin, Arnaud, Nigon, Delphine, Tobon, Gabriel, Cornillet, Martin, Schaeverbeke, Thierry, Chiocchia, Gilles, Nicaise-Roland, Pascale, Nogueira, Leonor, Serre, Guy, Cantagrel, Alain, Ruyssen-Witrand, Adeline, Saraux, Alain, Centre de Physiopathologie Toulouse Purpan (CPTP), Université Toulouse III - Paul Sabatier (UT3), Université Fédérale Toulouse Midi-Pyrénées-Université Fédérale Toulouse Midi-Pyrénées-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS), Centre de Rhumatologie [CHU Toulouse], Pôle Inflammation, infection, immunologie et loco-moteur [CHU Toulouse] (Pôle I3LM Toulouse), Centre Hospitalier Universitaire de Toulouse (CHU Toulouse)-Centre Hospitalier Universitaire de Toulouse (CHU Toulouse), Hôpital de la Cavale Blanche - CHRU Brest (CHU - BREST ), Unité différenciation épidermique et auto-immunité rhumatoïde (UDEAR), Université Fédérale Toulouse Midi-Pyrénées-Université Fédérale Toulouse Midi-Pyrénées-Institut National de la Santé et de la Recherche Médicale (INSERM), Centre Hospitalier Universitaire de Toulouse (CHU Toulouse), Service de Rhumatologie [CHU Pellegrin], Groupe hospitalier Pellegrin, Infection et inflammation (2I), Université de Versailles Saint-Quentin-en-Yvelines (UVSQ)-Institut National de la Santé et de la Recherche Médicale (INSERM), AP-HP - Hôpital Bichat - Claude Bernard [Paris], Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP), Epidémiologie et analyses en santé publique : risques, maladies chroniques et handicaps (LEASP), CARBILLET, Véronique, Service de rhumatologie, Hôpital Purpan [Toulouse], CHU Toulouse [Toulouse]-CHU Toulouse [Toulouse], CHU Toulouse [Toulouse], Institut National de la Santé et de la Recherche Médicale (INSERM)-Université Toulouse III - Paul Sabatier (UT3), Université Fédérale Toulouse Midi-Pyrénées-Université Fédérale Toulouse Midi-Pyrénées, Mécanismes, Conséquences et Modulation de l'Inflammation Ostéo-articulaire, Université Fédérale Toulouse Midi-Pyrénées-Université Fédérale Toulouse Midi-Pyrénées-Hôpital Purpan [Toulouse], CHU Toulouse [Toulouse]-CHU Toulouse [Toulouse]-IFR150-Institut National de la Santé et de la Recherche Médicale (INSERM), Immunologie et Pathologie (EA2216), Université de Brest (UBO)-IFR148, CHRU Brest - Service de Rhumatologie (CHU - BREST - Rhumato), Centre Hospitalier Régional Universitaire de Brest (CHRU Brest), Laboratoire de Biologie Cellulaire et Cytologie, Département de Rhumatologie, Université de Bordeaux (UB)-CHU Bordeaux [Bordeaux], Institut National de la Santé et de la Recherche Médicale (INSERM)-Université de Versailles Saint-Quentin-en-Yvelines (UVSQ), Laboratoire d'Immunologie 'Autoimmunité et Hypersensibilités' [AP-HP Hôpital Bichat, Paris], Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP), Centre d'Investigation Clinique (CIC - Brest), Université de Brest (UBO)-Institut National de la Santé et de la Recherche Médicale (INSERM), Lymphocyte B et Auto-immunité (LBAI), Université de Brest (UBO)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Institut Brestois Santé Agro Matière (IBSAM), and Université de Brest (UBO)

Subjects
MESH: Fatigue, MESH: Antirheumatic Agents, [SDV]Life Sciences [q-bio], MESH: Infliximab, Autoimmunity, Early Arthritis, Fibrinogen, medicine.disease_cause, Gastroenterology, pronostic radiographique, Early Rheumatoid Arthritis, [SDV.MHEP.MI]Life Sciences [q-bio]/Human health and pathology/Infectious diseases, Immunology and Allergy, MESH: Incidence, skin and connective tissue diseases, MESH: Treatment Outcome, MESH: Aged, MESH: Xerostomia, [SDV.MHEP.RSOA] Life Sciences [q-bio]/Human health and pathology/Rhumatology and musculoskeletal system, MESH: Middle Aged, biology, MESH: Endpoint Determination, anticorps anti vimentine citrullinée mutée, 3. Good health, MESH: Reproducibility of Results, [SDV.MHEP.RSOA]Life Sciences [q-bio]/Human health and pathology/Rhumatology and musculoskeletal system, Cohort, [SDV.MHEP.MI] Life Sciences [q-bio]/Human health and pathology/Infectious diseases, MESH: Rituximab, Mutated citrullinated vimentin, Antibody, medicine.drug, musculoskeletal diseases, medicine.medical_specialty, polyarthrite rhumatoïde débutante, Immunology, Rheumatology, Internal medicine, medicine, MESH: Outcome Assessment (Health Care), MESH: Blood Sedimentation, MESH: Humans, business.industry, Autoantibody, MESH: Adult, medicine.disease, MESH: Male, MESH: Sjogren's Syndrome, Ant-CCP, MESH: Netherlands, biology.protein, business, MESH: Female, Rheumatism, [SDV.MHEP]Life Sciences [q-bio]/Human health and pathology, anticorps anti peptides citrullinés
Abstract

Objectives: We compared the ability of antibodies against cyclic citrullinated peptides (anti-CCP2), against mutated citrullinated vimentin (anti-MCV) and against citrullinated fibrinogen (AhFibA) to predict 1 year rapid radiographic progression (RRP; total Sharp score variation ≥5 points), in early rheumatoid arthritis (RA).Methods: We analysed 566 patients from the ESPOIR cohort with early RA fulfilling the 2010 American College of Rheumatology/European League Against Rheumatism (ACR/EULAR) criteria at year 1. We assayed the 3 anticitrullinated peptide antibodies (ACPA) tests on baseline sera. We compared the performance of these 3 ACPA tests to predict first-year RRP, by comparing areas under the receiver operating characteristic curves (ROCs). We assessed the 1 year RRP risk by ACPA titres. We used a logistic multivariate regression to analyse RRP risk in terms either of ACPA positivity or titre: high (>3 times the N cut-off) and low (1 to 3N).Results: 145 patients displayed RRP. Areas under the ROCs were similar (0.60) for the 3 tests. High ACPA titres were associated with 1 year RRP, whatever the test was, and with similar ORs. Low+ anti-MCV titres were not associated with 1-year RRP, whereas low+ anti-CCP2 titres (p=0.0226) and low+ AhFibA titres (p=0.0332) were significantly associated. In multivariate analysis, 1 year RRP was associated with anti-CCP2 positivity (p, ObjectifsNous avons comparé la capacité des anticorps anti-CCP2, anti vimentine citrullinée mutée (anti-MCV) et anti fibrinogène humain citrulliné (AhFibA), à prédire la progression radiographique rapide à 1 an (RRP; variation du score de Sharp total ≥ 5 points), dans la polyarthrite rhumatoïde débutante (PR). MéthodesNous avons analysé 566 patients de la cohorte ESPOIR, présentant une PR débutante satisfaisant aux critères 2010 ACR/EULAR à la première année. La prédiction de la RRP à 1 an a été analysée par des courbes ROC pour les 3 ACPA évalués par sérologie à l’inclusion. Nous avons évalué l’association entre les titres d’ACPA et le risque de RRP à 1 an. Une régression logistique multivariée a été utilisée pour analyser le risque de RRP, en termes de positivité ou de titre élevé (>3 fois le seuil de positivité N) et faible (1 à 3N) des ACPA. RésultatsLes aires sous les courbes ROC étaient similaires (0,60) pour les 3 anticorps. Les titres faibles d’anti-MCV n’étaient pas associés à la RRP, contrairement aux titres faibles d’anti-CCP2 (p=0,0226) et d’AhFibA (p=0,0332). En analyse multivariée, la RRP à 1 an était associée aux titres élevés d’anti-MCV (p

Published
2015
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45. Allergological workup with half‐dose challenge in iodinated contrast media hypersensitivity.

Author

Soria, Angèle, Masson, Nathalie, Vial‐Dupuy, Amandine, Gaouar, Hafida, Amsler, Emmanuelle, Chollet‐Martin, Sylvie, Nicaise‐Roland, Pascale, Autegarden, Jean‐Eric, and Barbaud, Annick

Subjects
RADIOGRAPHIC contrast media, ALLERGIES, ANTIALLERGIC agents
Abstract

The article offers information on the diagnosis of hypersensitivity reaction (HSR) to iodinated contrast media (ICM) is challenging when based on clinical history and skin tests. It mentions the objective of this study was to determine the negative predictive value (NPV) for skin tests as compared with the intravenous provocation tests (IPT) 50 mL; and also mentions the IPT was reduced to 10 mL with glomerular filtration rate (GFR).

Published
2019
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46. Comparison of Basophil Activation Test and Skin Testing Performances in NMBA Allergy

Author

Dewachter, Pascale, Chollet-Martin, Sylvie, Mouton-Faivre, Claudie, de Chaisemartin, Luc, and Nicaise-Roland, Pascale

Abstract

Neuromuscular blocking agents (NMBAs) are the main agents involved during perioperative immediate hypersensitivity. The etiological diagnosis (IgE-mediated allergy vsnonallergy) is linked to the clinical presentation together with tryptase and histamine levels and skin test results. The role of basophil activation test (BAT) needs to be better defined in this setting.

Published
2024
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47. Effect of rapid desensitization on platelet inhibition and basophil activation in patients with aspirin hypersensitivity and coronary disease

Author

Manzo-Silberman, Stéphane, primary, Nicaise-Roland, Pascale, additional, Neukirch, Catherine, additional, Tubach, Florence, additional, Huisse, Marie-Geneviève, additional, Chollet-Martin, Sylvie, additional, Abergel, Hélène, additional, Driss, Fathi, additional, Alfaiate, Toni, additional, Ajzenberg, Nadine, additional, and Steg, Philippe Gabriel, additional

Published
2016
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50. Obstetrical APS: Is there a place for hydroxychloroquine to improve the pregnancy outcome?

Author

MS Reumatologie/Immunologie/Infectie, Infection & Immunity, Mekinian, Arsene, Costedoat-Chalumeau, Nathalie, Masseau, Agathe, Tincani, Angela, De Caroli, Sara, Alijotas-Reig, Jaume, Ruffatti, Amelia, Ambrozic, Ales, Botta, Angela, Le Guern, Véronique, Fritsch-Stork, Ruth, Nicaise-Roland, Pascale, Carbonne, Bruno, Carbillon, Lionel, Fain, Olivier, MS Reumatologie/Immunologie/Infectie, Infection & Immunity, Mekinian, Arsene, Costedoat-Chalumeau, Nathalie, Masseau, Agathe, Tincani, Angela, De Caroli, Sara, Alijotas-Reig, Jaume, Ruffatti, Amelia, Ambrozic, Ales, Botta, Angela, Le Guern, Véronique, Fritsch-Stork, Ruth, Nicaise-Roland, Pascale, Carbonne, Bruno, Carbillon, Lionel, and Fain, Olivier

Published
2015

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