Jhaveri Kenar D, Scheuer Abby, Cohen Jules, Gordon Bruce
Department of Medicine, New York Presbyterian Hospital, Weill Cornell Medical Center, New York, NY 10065, USA.
Transfus Apher Sci. 2009 Aug;41(1):19-22. doi: 10.1016/j.transci.2009.05.007. Epub 2009 Jun 10.
ADAMTS13 mediated thrombotic thrombocytopenic purpura (TTP) is an immunological disease that is very difficult to treat. Plasma exchange, with plasma replacement and steroids have been the first line of treatment for this condition. Ten to 20% of the patients either have no response or a partial response to the treatment. Refractory TTP has been treated in few case reports with anti-CD20 agents, intravenous gamma globulin, vincristine and splenectomy. We report two cases of refractory TTP that responded to multimodality immunosuppressive therapy that included splenectomy, intravenous gamma globulin, and cyclosporine after numerous plasma exchange treatments, steroids, rituximab and vincristine had failed to induce remission. Combining drugs that target T and B lymphocytes is a standard in organ transplantation and deserves more consideration in the treatment of severe and refractory autoimmune diseases such as TTP.
ADAMTS13介导的血栓性血小板减少性紫癜(TTP)是一种极难治疗的免疫性疾病。血浆置换、血浆替代及类固醇一直是该病的一线治疗方法。10%至20%的患者对该治疗无反应或仅有部分反应。少数病例报告中,难治性TTP采用抗CD20药物、静脉注射丙种球蛋白、长春新碱及脾切除术进行治疗。我们报告了两例难治性TTP病例,在多次血浆置换治疗、类固醇、利妥昔单抗及长春新碱均未能诱导缓解后,采用包括脾切除术、静脉注射丙种球蛋白及环孢素在内的多模式免疫抑制治疗取得了疗效。联合靶向T和B淋巴细胞的药物是器官移植的标准治疗方法,在治疗如TTP等严重难治性自身免疫性疾病时值得更多考虑。