Proceedings from the 2nd Next Gen Therapies for Systemic Juvenile Idiopathic Arthritis and Macrophage Activation Syndrome symposium held on October 3-4, 2019

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作者
Scott W. Canna
Grant S. Schulert
Adriana de Jesus
Alex Pickering
Hermine Brunner
Massimo Gadina
Stewart Levine
Raphaela Goldbach-Mansky
Jonathan Boutelle
Rashmi Sinha
Fabrizio DeBenedetti
Alexei Grom
机构
[1] University of Pittsburgh,Division of Rheumatology, Cincinnati Children’s Hospital Medical Center and Department of Pediatrics
[2] University of Cincinnati College of Medicine,undefined
[3] Intramural Research Program,undefined
[4] National Institute of Allergy and Infectious Diseases,undefined
[5] NIH,undefined
[6] Harvard Medical School,undefined
[7] SJIA Foundation,undefined
[8] Ospedale Pediatrico Bambino Gesù,undefined
来源
关键词
Systemic juvenile idiopathic arthritis; Macrophage activation syndrome; Hemophagocytic lymphohistiocytosis; Interferonopathy; Interstitial lung disease; Pulmonary alveolar proteinosis; Alveolar macrophages;
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摘要
For reasons poorly understood, and despite the availability of biological medications blocking IL-1 and IL-6 that have markedly improved overall disease control, children with Systemic Juvenile Idiopathic Arthritis (SJIA) are now increasingly diagnosed with life-threatening chronic complications, including hepatitis and lung disease (SJIA-LD). On October 3–4, 2019, a two-day meeting, NextGen Therapies for Systemic Juvenile Idiopathic Arthritis (SJIA) & macrophage activation syndrome (MAS) organized by the Systemic JIA Foundation (www.systemicjia.org/) in Washington, DC brought together scientists, clinicians, parents and FDA representatives with the objectives (1) to integrate clinical and research findings in MAS and SJIA-LD, and (2) to develop a shared understanding of this seemingly new pulmonary complication of SJIA. The current manuscript summarizes discussions and conclusions of the meeting.
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