Aoyama Yumi
Department of Dermatology, Okayama University Graduate School of Medicine, Dentistry, and Pharmaceutical Sciences.
Nihon Rinsho. 2012 Aug;70(8):1437-43.
High-dose intravenous immunoglobulin (HD-IVIg) is one of potential therapy to accelerate the pathogenic antibody degradation in pemphigus. Advantage and benefits of this therapy are non-immunosuppressive and less adverse effects. The clinical trial of HD-IVIg for pemphigus has proved that 400mg/kg/day for 5 days administration of IVIg is effective as an adjuvant therapy with systemic steroid therapy and/or immunosuppressive agents. Among the several mechanisms to explain the mode of action of IVIg, the neonatal Fc receptor for IgG (FcRn) plays important role for rapid clearance of pathogenic antibody in pemphigus induced by HD-IVIg. To monitor the serum IgG levels is necessary to predict the timing that the titer of anti-Dsg1 antibody starts to increase. Furthermore, the sufficient suppression of the antibody production in patients with severe disease activity is a key point for successful treatment with IVIg.
大剂量静脉注射免疫球蛋白(HD-IVIg)是加速天疱疮中致病性抗体降解的潜在治疗方法之一。这种治疗方法的优点是无免疫抑制作用且不良反应较少。HD-IVIg治疗天疱疮的临床试验证明,静脉注射免疫球蛋白按400mg/kg/天给药5天,作为全身类固醇治疗和/或免疫抑制剂的辅助治疗是有效的。在解释免疫球蛋白作用方式的几种机制中,IgG的新生儿Fc受体(FcRn)在HD-IVIg诱导的天疱疮中对致病性抗体的快速清除起重要作用。监测血清IgG水平对于预测抗桥粒芯糖蛋白1(Dsg1)抗体滴度开始升高的时间是必要的。此外,对疾病活动严重的患者充分抑制抗体产生是免疫球蛋白成功治疗的关键。