Zivković Sasa A
Department of Neurology, University of Pittsburgh Medical Center, PUH F875, 200 Lothrop Street, Pittsburgh, PA 15213, USA.
Expert Rev Neurother. 2006 Sep;6(9):1267-74. doi: 10.1586/14737175.6.9.1267.
Peripheral neuropathy associated with immunoglobulin (Ig)M gammopathy and anti-myelin-associated glycoprotein antibodies is frequently treatment-resistant and different treatment regimens carry substantial toxicity and side effects. More recently, the chimeric anti-CD20 monoclonal antibody rituximab has shown benefits in the treatment of peripheral neuropathy associated with IgM gammopathy with a favorable side-effect profile. There are no published reports of its use in the treatment of neuropathy associated with IgG and IgA gammopathies. Rituximab is usually given at 375 mg/m(2) intravenously with four weekly doses that may be repeated after 6-12 months. Large controlled studies are still pending but rituximab is an exciting and promising treatment offering another option in the treatment of peripheral neuropathy associated with IgM monoclonal gammopathy.
与免疫球蛋白(Ig)M 型丙种球蛋白病及抗髓鞘相关糖蛋白抗体相关的周围神经病常常对治疗耐药,不同的治疗方案具有显著的毒性和副作用。最近,嵌合抗 CD20 单克隆抗体利妥昔单抗已显示出在治疗与 IgM 型丙种球蛋白病相关的周围神经病方面具有益处,且副作用较小。尚无关于其用于治疗与 IgG 和 IgA 型丙种球蛋白病相关神经病的报道。利妥昔单抗通常以 375 mg/m²静脉注射,每周一次,共四次,6 - 12 个月后可重复给药。大型对照研究仍在进行中,但利妥昔单抗是一种令人兴奋且有前景的治疗方法,为治疗与 IgM 单克隆丙种球蛋白病相关的周围神经病提供了另一种选择。