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    Anakinra for the treatment of adult-onset Still's disease

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    AnakinraTreatmentAdu ... (1.288Mb)
    Identificadores
    URI: http://hdl.handle.net/10902/16102
    DOI: 10.1080/1744666X.2018.1536548
    ISSN: 1744-666X
    ISSN: 1744-8409
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    Autoría
    Castañeda Sanz, Santos; Atienza Mateo, Belén Autoridad Unican; Martín Varillas, José Luis; Serra López-Matencio, José María; González-Gay Mantecón, Miguel ÁngelAutoridad Unican
    Fecha
    2018
    Derechos
    © Taylor & Francis. This is an Accepted Manuscript of an article published by Taylor & Francis in Expert Review of Clinical Immunology on 2018, available online: http://wwww.tandfonline.com/10.1080/1744666X.2018.1536548
    Publicado en
    Expert Review of Clinical Immunology, 2018, 14:12, 979-992
    Editorial
    Taylor & Francis
    Enlace a la publicación
    https://doi.org/10.1080/1744666X.2018.1536548
    Palabras clave
    Anti-IL1-receptor drugs
    Anakinra
    Adult-onset Still´s disease (AOSD)
    Biologic agents
    Glucocorticoids
    Methotrexate
    Resumen/Abstract
    ABSTRACT: Introduction: Adult onset Still's disease (AOSD) is an uncommon systemic inflammatory disease on the clinical spectrum of autoinflammatory disorders. Its presentation and clinical course may result in several well-differentiated phenotypes: from a systemic and highly symptomatic pattern to a chronic articular pattern. Overproduction of numerous pro-inflammatory cytokines is observed in AOSD. Anakinra (ANK), a human interleukin (IL)-1R antagonist, has recently been approved in the EU for the treatment of AOSD. Areas covered: In this review, we discuss the main studies on the efficacy and safety on ANK for the treatment of AOSD. The vast majority of them are retrospective studies and case series. Expert commentary: Overall, ANK is an effective biologic agent for the treatment of AOSD, especially for the systemic pattern and also for those patients who have life-threatening complications, which frequently occur over the course of the disease. The initial dose usually indicated of ANK in adults is 100 mg/day subcutaneously, although dose reduction can be performed in some cases once the disease is under control. The safety profile of ANK is favorable and similar to that described in other rheumatic diseases. In conclusion, ANK is an effective and safe agent for the treatment of AOSD.
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    UNIVERSIDAD DE CANTABRIA

    Repositorio realizado por la Biblioteca Universitaria utilizando DSpace software
    Contacto | Sugerencias
    Metadatos sujetos a:licencia de Creative Commons Reconocimiento 4.0 España