Taaning E, Skov F
Department of Clinical Immunology and Blood Bank, Glostrup Hospital, Denmark.
Vox Sang. 1991;60(1):40-4. doi: 10.1111/j.1423-0410.1991.tb00869.x.
In two patients suffering from post-transfusion purpura, anti-Zwa was demonstrated in either eluates from autologous platelets harvested during the remission phase and after normalization of the platelet count. In both patients, platelet-associated immunoglobulin (PAIg) was demonstrated during the acute phase. PAIg disappeared concomitantly with recovery and, thus, seems to be associated with the thrombocytopenia. These data support the assumption that immunocomplexes are adsorbed nonspecifically to the platelets and cause destruction of autologous platelets lacking the corresponding antigen. An association between the IgG3 subclass of anti-Zwa antibodies and the destruction of autologous platelets was also seen.
在两名患有输血后紫癜的患者中,在缓解期采集的自体血小板洗脱液中以及血小板计数恢复正常后检测到了抗-Zwa。两名患者在急性期均检测到血小板相关免疫球蛋白(PAIg)。PAIg随着恢复而消失,因此似乎与血小板减少有关。这些数据支持这样的假设,即免疫复合物非特异性地吸附到血小板上,导致缺乏相应抗原的自体血小板被破坏。还发现抗-Zwa抗体的IgG3亚类与自体血小板的破坏之间存在关联。