Leung D Y, Moake J L, Havens P L, Kim M, Pober J S
Department of Pediatrics, Harvard Medical School, Boston, Massachusetts.
Lancet. 1988 Jul 23;2(8604):183-6. doi: 10.1016/s0140-6736(88)92287-8.
Sera from 13 of 14 children with acute haemolytic uraemic syndrome (HUS) contained complement-fixing IgG and IgM antibodies that lysed cultured human umbilical vein endothelial cells. In 3 of 3 sera tested, no lysis of dermal fibroblasts was observed. The endothelial cell antigen was lost after treatment of the cells with gamma interferon. In contrast, only 3 of 5 adult patients with acute, non-relapsing, thrombotic thrombocytopenic purpura (TTP) had lytic anti-endothelial antibodies and only 1 of these recognised an antigen lost upon gamma interferon treatment. None of 32 control sera contained lytic anti-endothelial cell antibodies. These data suggest that HUS involves a disorder of immunoregulation and that a unique class of anti-endothelial cell antibodies is produced that may take part in the pathogenesis of vascular injury in HUS.
14名患有急性溶血性尿毒症综合征(HUS)的儿童中,有13名儿童的血清含有能固定补体的IgG和IgM抗体,这些抗体可溶解培养的人脐静脉内皮细胞。在检测的3份血清中,未观察到对真皮成纤维细胞的溶解作用。用γ干扰素处理细胞后,内皮细胞抗原消失。相比之下,5名患有急性、非复发性血栓性血小板减少性紫癜(TTP)的成年患者中,只有3名具有溶血性抗内皮细胞抗体,其中只有1名识别出经γ干扰素处理后消失的抗原。32份对照血清中均未含有溶血性抗内皮细胞抗体。这些数据表明,HUS涉及免疫调节紊乱,并且会产生一类独特的抗内皮细胞抗体,这类抗体可能参与了HUS血管损伤的发病机制。