[凝胶离心技术(ID-Microtyping System)对木瓜蛋白酶试验红细胞抗体测定和分化的观察]。

E Strobel, J Wüllenweber
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引用次数: 0

摘要

背景:凝胶离心系统(ID Microtyping system, Fa。Diamed, Bensheim, FRG)是几种新方法中的一种,在过去几年中已经商业化用于检测针对红细胞抗原的抗体。材料和方法:1年来,我们在常规实验室采用凝胶离心法进行抗体筛选,每次进行3次试验:NaCl卡(室温)与未经处理的红细胞;2. NaCl卡(37℃)与木瓜蛋白酶处理的红细胞;利斯-库姆斯卡(37摄氏度)未经处理的红细胞。结果:两阶段木瓜蛋白酶试验发现了一些有趣的现象:在某些情况下,木瓜蛋白酶凝胶试验的敏感性高于本研究中测试的所有其他方法,即凝胶离心技术和试管离心技术。2. 有些反应似乎是针对患者自身的抗原(在恒河或基德系统中),但没有直接抗球蛋白试验阳性,也没有溶血的临床症状。3.有些血清显示的反应模式似乎具有明显的特异性,但它们不能被分配到制造商抗原谱中的任何抗原上。结论:在普遍推荐用凝胶离心法两阶段木瓜蛋白酶试验筛查抗体之前,有必要进一步研究仅用该技术检测到的抗体的临床价值。对于抗体鉴定,最好在小组工作表中作进一步声明。
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[Observations on antibody determination and differentiation with papain test erythrocytes using the gel centrifugation technique (ID-Microtyping System)].

Background: The gel centrifugation system (ID Microtyping System, Fa. Diamed, Bensheim, FRG) is one of several new methods, which has become commercially available within the last few years for the detection of antibodies against red blood cell antigens.

Materials and methods: During 1 year we used the gel centrifugation method for antibody screening in our routine laboratory by performing 3 tests each time: 1. NaCl card (room temperature) with untreated red cells; 2. NaCl card (37 degrees C) with papain-treated red cells, and 3. Liss-Coombs card (37 degrees C) with untreated red cells.

Results: The two-stage papain test revealed some interesting phenomena: 1. In some cases the sensitivity of the papain gel test is higher than that of all other methods tested in this study, namely in the gel centrifugation technique and in the tube centrifugation technique. 2. There are reactions which seem to be directed against patients' own antigens (in the Rhesus or Kidd system), but there are no positive direct antiglobulin test and no clinical signs of hemolysis. 3. Some sera show reaction patterns which seem to have a distinct specificity, but they cannot be assigned to any of the antigens in the manufacturer's antigenogram.

Conclusions: Before a general recommendation for antibody screening with the two-stage papain test in the gel centrifugation method can be given, further investigations about the clinical value of those antibodies which are detectable only by this technique are necessary. For antibody identification further declarations in the work sheet of the panel would be desirable.

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