Anakinra for the treatment of adult-onset Still's disease
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Castañeda Sanz, Santos; Atienza Mateo, Belén

Fecha
2018Derechos
© 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
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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