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酶替代疗法对戈谢病中免疫球蛋白异常血症的影响。

Effect of enzyme replacement therapy on gammopathies in Gaucher disease.

作者信息

Brautbar Ariel, Elstein Deborah, Pines Guy, Abrahamov Aya, Zimran Ari

机构信息

Gaucher Clinic, Shaare Zedek Medical Center, Jerusalem 91031, Israel.

出版信息

Blood Cells Mol Dis. 2004 Jan-Feb;32(1):214-7. doi: 10.1016/j.bcmd.2003.10.007.

Abstract

Chronic antigenic stimulation by the abnormal lipid storage has been postulated to be the mechanism underlying anecdotal reports of monoclonal and polyclonal gammopathies as well as an increased incidence of multiple myeloma in patients with Gaucher disease of all ages. With the advent of specific enzyme therapy, it has been possible to ascertain whether signs and symptoms associated with Gaucher disease are true features of the disorder by virtue of their responsiveness to treatment. The purpose of this study was to assess the incidence of polyclonal and monoclonal gammopathies in a large cohort of patients and the effect of enzyme treatment. All adult patients whose records of immunoglobulin levels were available at presentation or at the advent of enzyme replacement therapy (ERT), and who had been followed for 2 years or receiving ERT for at least 2 years, respectively, and for whom there were also immunoglobulin levels at their most recent follow-up, were included in the study. The incidence of polyclonal gammopathies ranged between 14% and 25% among treated and untreated patients. There were statistically significant percentage decreases per year of enzyme therapy in polyclonal but not monoclonal (1% of all patients) gammopathies. Among enzyme-treated patients, there was no statistically significant difference among patients with regard to spleen status or relative to other parameters of disease severity, hepatitis status, age or gender. This study represents the largest database of gammopathies among patients with Gaucher disease from a large referral clinic. Because there was no correlation of abnormal immunoglobulin levels with disease severity, etiology may not be related to lipid accumulation per se but perhaps reflects a secondary, enzyme-sensitive process, whereas monoclonal gammopathies remain unaffected.

摘要

异常脂质蓄积引起的慢性抗原刺激被认为是各年龄段戈谢病患者出现单克隆和多克隆丙种球蛋白病轶事报道以及多发性骨髓瘤发病率增加的潜在机制。随着特异性酶疗法的出现,通过观察与戈谢病相关的体征和症状对治疗的反应性,得以确定这些是否为该疾病的真实特征。本研究的目的是评估一大群患者中多克隆和单克隆丙种球蛋白病的发病率以及酶治疗的效果。所有成年患者纳入本研究,这些患者在就诊时或开始酶替代治疗(ERT)时可获取免疫球蛋白水平记录,分别随访了2年或接受ERT至少2年,且在最近一次随访时也有免疫球蛋白水平记录。在接受治疗和未接受治疗的患者中,多克隆丙种球蛋白病的发病率在14%至25%之间。多克隆丙种球蛋白病经酶治疗后每年有统计学显著意义的百分比下降,但单克隆丙种球蛋白病(占所有患者的1%)没有。在接受酶治疗的患者中,患者在脾脏状态或相对于疾病严重程度的其他参数、肝炎状态、年龄或性别方面没有统计学显著差异。本研究代表了一家大型转诊诊所中戈谢病患者丙种球蛋白病的最大数据库。由于异常免疫球蛋白水平与疾病严重程度无相关性,病因可能与脂质蓄积本身无关,而可能反映了一个继发性的、对酶敏感的过程,而单克隆丙种球蛋白病仍未受影响。

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