Serious infections in patients with VEXAS syndrome: data from the French VEXAS registry.
Benjamin de ValenceMarion DelauneYann NguyenVincent JachietMael HeibligAlexis JeanStanislas Riescher TuczkiewiczPierrick HennetonPhilippe GuilpainNicolas SchleinitzGuillaume Le GuennoHervé LobbesValentin LacombeSamuel ArdoisEstibaliz LazaroVincent LangloisRoderau OuthJulien VinitJean-Philippe MartellosioPaul DeckerThomas MoulinetYannick DieudonnéAdrien BigotLouis TerriouAlexandre VlakosBaptiste de MalepradeGuillaume DenisJonathan BronerMarie KostineSebastien HumbertFrancois LifermannMaxime SamsonSusann PechuzalAchille AoubaOlivier KosmiderJeremie DionSylvie GrosleronRim BourguibaBenjamin TerrierStéphanie Ducharme-BénardOlivier FainArsenne MekinianMarjolaine MorgandThibault ComontJérôme Hadjadjnull nullPublished in: Annals of the rheumatic diseases (2023)
mutation and treated with JAK inhibitors. The high frequency of atypical infections, especially in patients without treatment, may indicate an intrinsic immunodeficiency.