Brand A, Witvliet M, Claas F H, Eernisse J G
Department of Immunohaematology, University Medical Centre, Leiden, The Netherlands.
Br J Haematol. 1988 Aug;69(4):507-11. doi: 10.1111/j.1365-2141.1988.tb02407.x.
Intravenous gammaglobulin (IV-IgG) was administered to a patient with chronic idiopathic thrombocytopenic purpura due to an unusual IgM platelet autoantibody causing in vitro complement-dependent thrombocytoxicity and in vivo intravascular platelet destruction. After IV-IgG infusion the peripheral platelet count temporarily increased to normal values, the mean platelet survival time increased and the platelet sequestration pattern changed from intravascular to predominantly hepatic destruction. In vivo and in vitro observations in this patient illustrate a transient beneficial effect of gammaglobulin infusion due to interference with the complement-fixing autoantibodies against platelets.
一名患有慢性特发性血小板减少性紫癜的患者因一种不寻常的IgM血小板自身抗体导致体外补体依赖性血小板毒性和体内血管内血小板破坏而接受静脉注射丙种球蛋白(IV-IgG)治疗。静脉注射IV-IgG后,外周血小板计数暂时升至正常水平,平均血小板存活时间延长,血小板隔离模式从血管内破坏转变为主要是肝脏破坏。该患者的体内和体外观察结果表明,由于干扰了针对血小板的补体结合自身抗体,丙种球蛋白输注产生了短暂的有益效果。