Rapid and Sustained Remission of Systemic Juvenile Idiopathic Arthritis-Associated Macrophage Activation Syndrome Through Treatment With Anakinra and Corticosteroids

被引:110
作者
Bruck, Normi [1 ]
Suttorp, Meinolf [2 ]
Kabus, Maria [3 ]
Heubner, Georg [1 ,4 ]
Gahr, Manfred [1 ]
Pessler, Frank [1 ,5 ]
机构
[1] Tech Univ Dresden, Univ Childrens Hosp, Div Rheumatol & Immunol, Dresden, Germany
[2] Tech Univ Dresden, Univ Childrens Hosp, Div Hematol & Oncol, Dresden, Germany
[3] Med Ctr Dresden Neustadt, Dept Pediat, Braunschweig, Germany
[4] Pirna Med Ctr, Dept Pediat, Braunschweig, Germany
[5] Helmholtz Ctr Infect Res, Dept Infect Genet, Braunschweig, Germany
关键词
macrophage activation syndrome; recombinant interleukin 1 antagonist; systemic juvenile idiopathic arthritis; INTERLEUKIN-1 RECEPTOR ANTAGONIST; HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS; GUIDELINES;
D O I
10.1097/RHU.0b013e318205092d
中图分类号
R5 [内科学];
学科分类号
100201 [内科学];
摘要
We describe 2 patients with systemic juvenile idiopathic arthritis and macrophage activation syndrome. Treatment with recombinant interleukin 1 receptor antagonist (anakinra) and a corticosteroid rapidly induced remission, which could be maintained with anakinra monotherapy at a stable dose of 2 mg/kg per day. Pain at the injection site during the initial injections was the only adverse effect attributable to anakinra. Untoward effects of corticosteroid treatment were mild because prolonged therapy with high-dose corticosteroids could be avoided. These results suggest that early institution of interleukin 1 blockade merits further investigation for the treatment of macrophage activation syndrome and, perhaps, related conditions such as hemophagocytic lymphohistiocytosis.
引用
收藏
页码:23 / 27
页数:5
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