Escherchia coli 敗血症に合併した Acquired Bおよび Tk-polyagglutination の1例

Makiko Ozaki, S. Matsuda, Masataka Nishiyama, Toshimi Iura, K. Matsuzaki
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引用次数: 1

Abstract

We report on a patient who developed acquired B antigen and Tk polyagglutination in Escherichia coli( Ec oli)septicaemia during the course of ulcerative colitis. In vitro analysis showed that Ec oliwas the cause of the acquired B phenomenon. The level of intensity of both Tk and acquired B antigen changed simultaneously and both disappeared at the same time. Both antigens were also abolished by acetylation of the patient’ s red blood cells. These findings indicate that the Tk polyagglutination was closely related to the acquired B antigen. H activity decreased during the course of hospitalization. From the results of acetylation of the patient’ s red blood cells the decrease in H activity was explained by the fact that acquired B‑and Tk‑expressing red blood cells showed stronger than H activity of A1 red blood cells. The antigenic modification appeared prior to the onset of Ec olisepticaemia. This finding sug‑ gests that the early detection of blood abnormalities is helpful in the early diagnosis and proper treat‑ ment of these patients.
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Acquired B和Tk-polyagglutination合并Escherchia coli败血症的1例
我们报告了一例在溃疡性结肠炎过程中发生获得性B抗原和Tk多凝集的大肠杆菌败血症患者。体外分析表明,Ec olip是获得性B现象的原因。Tk和获得性B抗原强度同时变化,同时消失。这两种抗原也被患者红细胞的乙酰化所消除。这些结果表明Tk多凝集与获得性B抗原密切相关。H活性在住院期间下降。从患者红细胞乙酰化的结果来看,H活性降低的原因是获得性表达B -和Tk -的红细胞比A1红细胞的H活性更强。抗原修饰出现在大肠杆菌败血症发病之前。这一发现提示,早期发现血液异常有助于这些患者的早期诊断和适当治疗。
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