Intravenous immunoglobulins for relapses of systemic vasculitides associated with antineutrophil cytoplasmic autoantibodies

被引:121
作者
Martinez, Valerie [1 ]
Cohen, Pascal [1 ]
Pagnoux, Christian [1 ]
Vinzio, Stephane [1 ]
Mahr, Alfred [1 ]
Mouthon, Luc [1 ]
Sailler, Laurent [1 ]
Delaunay, Claire [1 ]
Sadoun, Alain [2 ]
Guillevin, Loic [1 ]
机构
[1] Univ Paris 05, Assistance Publ Hop Paris, Dept Internal Med,Hop Cochin, Reference Ctr Rare Dis Vasculitis & Scleroderma, F-75679 Paris 14, France
[2] Lab Francais Fractionnement Biotechnol, Courtaboeuf, France
来源
ARTHRITIS AND RHEUMATISM | 2008年 / 58卷 / 01期
关键词
D O I
10.1002/art.23147
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective. To evaluate at 9 months and 24 months the safety and efficacy of intravenous immunoglobulins (IVIGs) administered for 6 months to treat relapses of Wegener's granulomatosis (WG) or microscopic polyangiitis (MPA) occurring either under treatment or during the year following discontinuation of corticosteroids and/or immunosuppressants. Methods. Patients received IVIGs (0.5 gm/kg/day for 4 days) as additional therapy administered monthly for 6 Months and were assessed every 3-6 months. Corticosteroids could be maintained or reintroduced at the time of relapse; immunosuppressants could be continued but could not be reintroduced. At months 9 (end point) and 24 (followup), the following information was collected: complete or partial remission, relapse as assessed with the Birmingham Vasculitis Activity Score (BVAS) 2005, and tolerance and safety of WIG therapy. Results. Twenty-two Caucasian patients (7 men and 15 women) were studied: 19 had WG, and 3 had MPA. Their median age was 53 years (range 19-75 years), and their median duration of systemic vasculitis was 27 months (range 7-109 months). Their median BVAS 2005 score was 11 (range 3-25). At study entry, 21 patients were ANCA positive, and 21 patients were taking steroids and/or immunosuppressants. All patients experiencing relapse were treated with the same drug(s) plus IVIGs. All patients initially responded to WIG therapy. By month 9, 13 patients had complete remission, 1 had partial remission, 7 had relapse, and 1 had treatment failure. In 8 of the 14 patients who had remission, the response persisted at month 24. Seven patients experienced minor side effects. Conclusion. IVIGs induced complete remissions of relapsed ANCA-associated vasculitides in 13 of 22 patients at month 9. Because of the good safety and tolerance profiles of IVIGs, these agents can be included in a therapeutic strategy with other drugs used to treat relapses of WG or MPA.
引用
收藏
页码:308 / 317
页数:10
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