JAK inhibitors are effective in a subset of patients with juvenile dermatomyositis: a monocentric retrospective study

  • Tom Le Voyer
    Department of Paediatric Hematology-Immunology and Rheumatology, Necker-Enfants Malades Hospital, Assistance Publique-Hôpitaux de Paris, Reference Centre for Rheumatic, Autoimmune and Systemic Diseases in Children
  • Cyril Gitiaux
    Reference Centre for Neuromuscular Diseases, Necker-Enfants Malades Hospital, Assistance Publique-Hôpitaux de Paris
  • François-Jérôme Authier
    INSERM U955-Team Relaix, Faculty of Medicine, University of Paris-Est Creteil
  • Christine Bodemer
    Department of Pediatric Dermatology and Dermatology, National Reference Centre for Genodermatosis and Rare Diseases of the Skin, Hôpital Necker-Enfants Malades, Assistance Publique-Hôpitaux de Paris, Université Paris Descartes
  • Isabelle Melki
    Department of Paediatric Hematology-Immunology and Rheumatology, Necker-Enfants Malades Hospital, Assistance Publique-Hôpitaux de Paris, Reference Centre for Rheumatic, Autoimmune and Systemic Diseases in Children
  • Pierre Quartier
    Department of Paediatric Hematology-Immunology and Rheumatology, Necker-Enfants Malades Hospital, Assistance Publique-Hôpitaux de Paris, Reference Centre for Rheumatic, Autoimmune and Systemic Diseases in Children
  • Florence Aeschlimann
    Department of Paediatric Hematology-Immunology and Rheumatology, Necker-Enfants Malades Hospital, Assistance Publique-Hôpitaux de Paris, Reference Centre for Rheumatic, Autoimmune and Systemic Diseases in Children
  • Arnaud Isapof
    Department of Paediatric Neurology, Reference Centre for Neuromuscular Diseases, Armand Trousseau Hospital, Assistance Publique-Hôpitaux de Paris
  • Jean Philippe Herbeuval
    Chemistry and Biology, Modelling and Immunology for Therapy, CNRS, UMR8601, Université Paris Descartes
  • Vincent Bondet
    Translational Immunology Lab, Institut Pasteur
  • Jean-Luc Charuel
    Laboratory of Immunology, La Pitié Hospital, Assistance Publique-Hôpitaux de Paris, Paris, France
  • Marie-Louise Frémond
    Laboratory of Neurogenetics and Neuroinflammation, Imagine Institute, Paris University
  • Darragh Duffy
    Translational Immunology Lab, Institut Pasteur
  • Mathieu P Rodero
    Chemistry and Biology, Modelling and Immunology for Therapy, CNRS, UMR8601, Université Paris Descartes
  • Brigitte Bader-Meunier
    Department of Paediatric Hematology-Immunology and Rheumatology, Necker-Enfants Malades Hospital, Assistance Publique-Hôpitaux de Paris, Reference Centre for Rheumatic, Autoimmune and Systemic Diseases in Children

書誌事項

公開日
2021-02-12
権利情報
  • https://academic.oup.com/journals/pages/open_access/funder_policies/chorus/standard_publication_model
DOI
  • 10.1093/rheumatology/keab116
公開者
Oxford University Press (OUP)

この論文をさがす

説明

<jats:title>Abstract</jats:title> <jats:sec> <jats:title>Objective</jats:title> <jats:p>To evaluate the efficacy and safety of Janus kinase inhibitors (JAKis) in JDM.</jats:p> </jats:sec> <jats:sec> <jats:title>Methods</jats:title> <jats:p>We conducted a single-centre retrospective study of patients with JDM treated by JAKi with a follow-up of at least 6 months. Proportion of clinically inactive disease (CID) within 6 months of JAKi initiation was evaluated using PRINTO criteria and skin Disease Activity Score. Serum IFN-α concentration was measured by Simoa assay.</jats:p> </jats:sec> <jats:sec> <jats:title>Results</jats:title> <jats:p>Nine refractory and one new-onset patients with JDM treated with ruxolitinib (n = 7) or baricitinib (n = 3) were included. The main indications for treatment were refractory muscle involvement (n = 8) and ulcerative skin disease (n = 2). CID was achieved in 5/10 patients (two/two anti-MDA5, three/four anti-NXP2, zero/three anti-TIF1γ-positive patients) within 6 months of JAKi introduction. All responders could withdraw plasmatic exchange, immunoadsorption and other immunosuppressive drugs. The mean daily steroid dose decreased from 1.1 mg/kg (range 0.35–2 mg/kg/d) to 0.1 (range, 0–0.3, P = 0.008) in patients achieving CID, and was stopped in two. Serum IFN-α concentrations were elevated in all patients at the time of treatment initiation and normalized in both responder and non-responder. A muscle biopsy repeated in one patient 26 months after the initiation of JAKi, showed a complete restoration of muscle endomysial microvascular bed. Herpes zoster and skin abscesses developed in three and two patients, respectively.</jats:p> </jats:sec> <jats:sec> <jats:title>Conclusion</jats:title> <jats:p>JAKis resulted in a CID in a subset of new-onset or refractory patients with JDM and may dramatically reverse severe muscle vasculopathy. Overall tolerance was good except for a high rate of herpes zoster infection.</jats:p> </jats:sec>

収録刊行物

  • Rheumatology

    Rheumatology 60 (12), 5801-5808, 2021-02-12

    Oxford University Press (OUP)

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