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[用于乳胶诊断试验的嗜异性传染性单核细胞增多症抗原。I. 抗原分离方法及其血清学活性]

[Heterophile infectious mononucleosis antigen used in the latex diagnostic test. I. A method of antigen isolation and its serologic activity].

作者信息

Kałuzewski S, Jagielski M

机构信息

Zakład Bakteriologii PZH w Warszawie.

出版信息

Med Dosw Mikrobiol. 1990;42(1-2):68-76.

PMID:1964993
Abstract

The aim of this study was to elaborate a method of heterophile mononucleosis antigen preparation useful for latex coating. This antigen was isolated from bovine red blood cells stroma by the technique of Schwarzweiss and Tomcsik with author's own modification, in which introductory extraction of erythrocytes stroma ++ was performed by means of trichloracetic acid, aqueous extraction and elution of active substance with 80% ethanol. Besides of heterophile antigen preparation obtained by the method of Schwerzweiss and Tomcsik (preparation S-T) two serologically++ active preparations were obtained (fraction I and IV), which ability to inhibit PBD agglutinating reaction and bovine red blood cells haemolysis was 16 and 8 times lower, respectively, than S-T preparation. The preparation of heterophile mononucleosis antigen obtained differed in latex coating efficacy. In order to prepare latex reagent MZ-I (from fraction I) a solution of preparation of 125 micrograms/ml concentration was used, for MZ-II (from fraction IV)--50 micrograms and for MZ-III (from preparation S-T)--15 micrograms/ml. The reagent MZ-I showed, the highest activity in agglutinating test with human serum containing heterophile mononucleosis antibodies while two others reacted with 2-4 times lover serum dilutions. Similar differentiated reactivity with these reagents was found in latex test with 15 sera from patients suspected of having infectious mononucleosis.

摘要

本研究的目的是精心制定一种适用于乳胶包被的嗜异性单核细胞增多症抗原制备方法。该抗原是通过施瓦茨魏斯和托姆西克技术并经作者本人修改后从牛红细胞基质中分离出来的,其中红细胞基质++的初步提取是通过三氯乙酸进行的,活性物质的水相提取和用80%乙醇洗脱。除了通过施瓦茨魏斯和托姆西克方法获得的嗜异性抗原制剂(制剂S-T)外,还获得了两种血清学++活性制剂(组分I和IV),它们抑制PBD凝集反应和牛红细胞溶血的能力分别比S-T制剂低16倍和8倍。所获得的嗜异性单核细胞增多症抗原制剂在乳胶包被效果上有所不同。为了制备乳胶试剂MZ-I(来自组分I),使用了浓度为125微克/毫升的制剂溶液,对于MZ-II(来自组分IV)为50微克,对于MZ-III(来自制剂S-T)为15微克/毫升。试剂MZ-I在与含有嗜异性单核细胞增多症抗体的人血清的凝集试验中显示出最高活性,而另外两种试剂与低2-4倍的血清稀释度反应。在对15例疑似传染性单核细胞增多症患者的血清进行乳胶试验时,也发现了与这些试剂类似的差异反应性。

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