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伴有蛋白异常血症的血管免疫母细胞性淋巴结病中血型抗原的改变。

Alterations of blood group antigens in angio-immunoblastic lymphadenopathy with dysproteinemia.

作者信息

Kajii E, Ueki J, Ikemoto S, Miura Y

出版信息

Am J Med Sci. 1986 Sep;292(3):164-7. doi: 10.1097/00000441-198609000-00009.

Abstract

Antigen analysis of the red cell membrane in a patient with angio-immunoblastic lymphadenopathy with dysproteinemia (AILD) with red cell autoantibody revealed that four blood group antigens had been acquired. These four antigens consisted of S of MNSs blood group, Lua of Lutheran blood group, and K and Kpa of Kell-Cellano blood group. These antigens disappeared and the Coombs' test became negative after complete remission induced by combination chemotherapy. Free amino acid analysis after Dispase treatment of red cell membrane suggested that the antigenic modifications were associated with abnormal composition of amino acids.

摘要

对一名患有血管免疫母细胞性淋巴结病伴蛋白异常血症(AILD)且有红细胞自身抗体的患者的红细胞膜进行抗原分析发现,其获得了四种血型抗原。这四种抗原包括MNSs血型的S抗原、路德血型的Lua抗原以及凯尔 - 塞拉诺血型的K和Kpa抗原。在联合化疗诱导完全缓解后,这些抗原消失,库姆斯试验转为阴性。用Dispase处理红细胞膜后的游离氨基酸分析表明,抗原修饰与氨基酸组成异常有关。

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