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SWORD: A simplified desensitization protocol for enzyme replacement therapy in adult Pompe disease

机译:剑:成人庞贝氏病的酶替代疗法的简化脱敏方案

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Pompe disease is an inherited lysosomal disease in which there is a decrease or absence of acid alpha-glucosidase activity. This enzyme defect induces glycogen storage in different tissues, especially muscle and heart, resulting in muscle weakness, respiratory failure and heart disease. Substitutive enzyme replacement therapy (ERT) dispensed every two weeks is the only treatment that has shown benefits. However, this treatment induces hypersensitivity for half of the treated patients. Reactions range from mild to severe, sometimes requiring ERT suspension and anti-anaphylaxis drug administration. Understandably, high amount of acid alpha-glucosidase infusion seems to be identified by the immune system as a danger associated molecular pattern, and induce an immune reaction, involving sometimes, but not always, immunoglobulin E (IgE) production and activating mast and basophil polynuclear cells. Considering the lack of therapeutic alternatives and the proved benefit of ERT, desensitization finds its place here. We hereby report the case of a patient for whom a simplified desensitization protocol ("SWORD": Start With One Regular Drop) was successfully achieved, allowing ERT to be pursued, resulting eventually in clinical improvement. (C) 2016 Published by Elsevier B.V.
机译:庞贝病是一种遗传性溶酶体病,其中酸性α-葡萄糖苷酶活性降低或不存在。这种酶缺陷会导致糖原在不同组织(尤其是肌肉和心脏)中的存储,从而导致肌肉无力,呼吸衰竭和心脏病。每两周进行一次替代酶替代疗法(ERT)是唯一显示出益处的疗法。然而,这种治疗对一半接受治疗的患者引起超敏反应。反应范围从轻度到严重,有时需要ERT悬浮和抗过敏药给药。可以理解,大量的酸性α-葡萄糖苷酶输注似乎被免疫系统识别为与危险相关的分子模式,并诱发免疫反应,有时但不总是涉及免疫球蛋白E(IgE)产生并激活肥大和嗜碱性粒细胞细胞。考虑到缺乏治疗选择和ERT的公认优势,脱敏在这里找到了位置。我们在此报告一例患者,该患者成功实现了简化的脱敏方案(“ SWORD”:从一个常规滴剂开始),可以进行ERT治疗,最终导致临床改善。 (C)2016由Elsevier B.V.发布

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