Zum Mechanismus des Witebsky-Tests

F. Mehnert , K. Hummel
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Abstract

The assumption that immune and normal alloantibodies of the AB0 system could be distinguished by partial neutralization with soluble specific blood group substance (Witebsky test) has been reexamined. The following results were presented:

  • 1.

    AB0 alloantibodies in both normal and immune sera as well as their IgG and IgM preparations were inhibited by their homologous soluble specific blood group substances.

  • 2.

    Anti-A and anti-B immune antibodies as well as normal antibodies of the IgG class were found to be strong hemagglutinins in a saline medium; therefore they have to be called «complete» hemagglutinins as have anti-A and anti-B antibodies of the class IgM too.

  • 3.

    AB0 alloantibodies in both IgG and IgM preparations were able to form precipitation pellets with their homologous soluble specific blood group substances. IgM revealed a stronger precipitation power as IgG.

  • 4.

    Agglutination reaction in saline was inhibited by the 50-200-fold blood group substance concentration needed for a optimal precipitation reaction, where as agglutination of enzyme treated erythrocytes or red cells tested with antiglobulin (Coombs) sera was inhibited by a 20,000-80,000-fold concentration of the blood group substances.

  • 5.

    Soluble antigen-antibody complexes, prepared from solubilized precipitates or from Witebsky test mixtures using chromatography, ultracentrifuge or ultrafiltration for separation were able to agglutinate erythrocytes in the antiglobulin or papain test

.

Following conclusions were drawn:

  • A.

    Soluble antigen-antibody complexes are the main component leading to a positive Witebsky test.

  • B.

    The mechanism of the Witebsky test as it has to be assumed in respect to our findings do not allow to distinguish immune and normal alloantibodies resp. IgG and IgM alloagglutinins in the AB0 system

.
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witebsky测试的机制
AB0系统的免疫和正常同种抗体可以通过可溶性特异性血型物质的部分中和(Witebsky试验)来区分的假设已被重新检验。研究结果如下:1。正常和免疫血清中的AB0同种异体抗体及其IgG和IgM制剂均被其同源可溶性特异性血型物质抑制。在生理盐水培养基中发现抗a和抗b免疫抗体以及IgG类正常抗体为强血凝素;因此,它们必须被称为“完全”血凝素,因为它们也具有IgM类的抗a和抗b抗体。IgG和IgM制剂中的AB0同种异体抗体均能与其同源可溶性特异性血型物质形成沉淀微球。IgM表现出比IgG.4更强的降水能力。生理盐水中的凝集反应被最佳沉淀反应所需的50-200倍血型物质浓度所抑制,而酶处理红细胞或用抗球蛋白(Coombs)血清测试的红细胞的凝集反应被20,000-80,000倍血型物质浓度所抑制。可溶性抗原-抗体复合物,从溶解的沉淀物或Witebsky试验混合物中制备,使用色谱、超离心或超滤进行分离,能够在抗球蛋白或木瓜蛋白酶试验中凝集红细胞。得出以下结论:A。可溶性抗原抗体复合物是导致Witebsky试验阳性的主要成分。根据我们的研究结果,我们必须假设Witebsky试验的机制不能区分免疫和正常的同种异体抗体。IgG和IgM异位凝集素在AB0系统中的作用。
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