Loebstein R, Dalal I, Nisbet-Brown E, Berkovitch M, Meydan N, Andrews D, Loubser M D, Koren G, Roifman C M, Olivieri N F
Division of Haematology/Oncology, University of Toronto, Ontario, Canada.
Br J Haematol. 1997 Sep;98(3):597-600. doi: 10.1046/j.1365-2141.1997.2463064.x.
Short-term deferiprone may reduce body iron in some patients with thalassaemia major. Concerns regarding potential immunosuppressive effects of deferiprone have been raised from results of animal studies and case reports in humans. We studied immune function in 57 thalassaemia patients: 36 treated with deferiprone (L1; CP020) and 21 treated with desferrioxamine (DFO). Circulating B lymphocytes were increased in all patient groups. No differences were detected between treatment groups in percentages of circulating lymphocytes, concentrations of IgG, IgM or IgA, specific antibody titres, complement levels, or in vitro lymphocyte proliferation. No clinically important infections were observed in any patient. These data suggest that no clinical or laboratory changes consistent with immuno-suppression or immunodeficiency are observed during deferiprone therapy.
短期使用去铁酮可能会降低一些重型地中海贫血患者体内的铁含量。动物研究结果和人类病例报告引发了对去铁酮潜在免疫抑制作用的担忧。我们对57例地中海贫血患者的免疫功能进行了研究:36例接受去铁酮(L1;CP020)治疗,21例接受去铁胺(DFO)治疗。所有患者组的循环B淋巴细胞均增加。治疗组在循环淋巴细胞百分比、IgG、IgM或IgA浓度、特异性抗体滴度、补体水平或体外淋巴细胞增殖方面均未检测到差异。任何患者均未观察到具有临床意义的感染。这些数据表明,在去铁酮治疗期间未观察到与免疫抑制或免疫缺陷一致的临床或实验室变化。