Gounder M P, Baker D, Saletan S, Monheit A G, Hultin M B, Coller B S
Obstet Gynecol. 1986 May;67(5):741-6. doi: 10.1097/00006250-198605000-00026.
Intravenous gammaglobulin (IVIgG) was recently introduced for the treatment of idiopathic thrombocytopenic purpura (ITP). Reported is a previously splenectomized patient who had a severe exacerbation of her ITP during pregnancy and was managed with large doses of IVIgG throughout the second half of her pregnancy. She also had an autoimmune IgG erythrocyte panagglutinin on her red blood cells and in her serum, but only minimal evidence of hemolysis. There was little or no transplacental passage of her autoimmune antibodies since she delivered a normal fetus after 34 weeks of gestation who had a normal platelet count and no evidence of an antierythrocyte antibody. Interestingly, at the time of delivery the mother's serum IgG was dramatically elevated, but the cord serum IgG was normal for the length of gestation, indicating the presence of a dramatic and abnormal difference in IgG between maternal and fetal blood. This raises the possibility that the IVIgG therapy may have actually prevented transplacental passage of the pathological antibodies.
静脉注射丙种球蛋白(IVIgG)最近被用于治疗特发性血小板减少性紫癜(ITP)。据报道,有一位曾接受脾切除术的患者,在孕期ITP病情严重加重,在妊娠后半期接受了大剂量IVIgG治疗。她的红细胞和血清中还存在自身免疫性IgG红细胞全凝集素,但仅有轻微溶血迹象。由于她在妊娠34周后分娩出一名血小板计数正常且无抗红细胞抗体迹象的正常胎儿,其自身免疫抗体几乎没有或没有经胎盘传递。有趣的是,分娩时母亲的血清IgG显著升高,但脐带血清IgG在相应孕周时正常,这表明母血和胎儿血之间的IgG存在显著且异常的差异。这增加了IVIgG治疗实际上可能阻止了病理性抗体经胎盘传递的可能性。