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dc.rights.licenseopenen_US
dc.contributor.authorVIAL, G.
dc.contributor.authorGENSOUS, N.
hal.structure.identifierComposantes innées de la réponse immunitaire et différenciation [CIRID]
hal.structure.identifierService de médecine interne et maladies infectieuses [Bordeaux]
hal.structure.identifierHôpital Saint-André
hal.structure.identifierCHU Bordeaux
hal.structure.identifierHôpital Saint-André
hal.structure.identifierImmunology from Concept and Experiments to Translation = Immunologie Conceptuelle, Expérimentale et Translationnelle [ImmunoConcept]
hal.structure.identifierBiologie des maladies cardiovasculaires = Biology of Cardiovascular Diseases
dc.contributor.authorDUFFAU, Pierre
dc.date.accessioned2022-05-02T08:57:15Z
dc.date.available2022-05-02T08:57:15Z
dc.date.issued2021
dc.identifier.issn0248-8663en_US
dc.identifier.urihttps://oskar-bordeaux.fr/handle/20.500.12278/139949
dc.description.abstractEnThe CD40-CD40 ligand (CD40L) pathway is a backbone of communication between cells of the immune system. It makes it possible to generate a proinflammatory signal and thus participates in the pathogenesis of dysimmune diseases, transplant rejection and atherosclerosis. Because of this therapeutic target of choice, several generations of anti-CD40L monoclonal antibodies have emerged since the 1990s. The first generation of antibodies was responsible for thromboembolic toxicity for which the mechanisms are starting to be defined. New generations of antibodies were designed to overcome this toxicity and are still being developed in lupus, rheumatoid arthritis, Sjogren's syndrome or immunologic thrombocytopenia. In addition to these targeted therapies, there are data suggesting the impact of several drugs among molecules used in cardiology and clinical immunology on the level of CD40L. The objective of this review is to recall the clinical issues related to the CD40-CD40L axis and to present current or future treatments that block CD40L which would allow clinicians to diversify their options for managing dysimmune diseases.
dc.language.isoFRen_US
dc.subject.enAutoimmunity
dc.subject.enCD40 ligand
dc.subject.enInflammation
dc.subject.enMonoclonal antibody
dc.subject.enTargeted therapy
dc.title.enThe CD40-CD40L axis: Current and future implications in clinical immunology [L'axe CD40-CD40L : implications actuelles et futures en immunologie clinique]
dc.typeArticle de revueen_US
dc.identifier.doi10.1016/j.revmed.2021.02.005en_US
dc.subject.halSciences du Vivant [q-bio]/Immunologieen_US
dc.identifier.pubmed33674076en_US
bordeaux.journalRevue de Medecine Interneen_US
bordeaux.page722-728en_US
bordeaux.volume42en_US
bordeaux.hal.laboratoriesImmunoConcEpT - UMR 5164en_US
bordeaux.issue10en_US
bordeaux.institutionUniversité de Bordeauxen_US
bordeaux.institutionCNRSen_US
bordeaux.peerReviewedouien_US
bordeaux.inpressnonen_US
hal.identifierhal-03656484
hal.version1
hal.date.transferred2022-05-02T08:57:16Z
hal.exporttrue
dc.rights.ccPas de Licence CCen_US
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