Holmberg K, Nord C E, Wadström T
Infect Immun. 1975 Aug;12(2):387-97. doi: 10.1128/iai.12.2.387-397.1975.
Standard preparations of crude cytoplasmic and whole cell-associated antigen mixtures of Actinomyces israelii were analyzed by crossed immunoelectrophoresis (CIE), with a standard polyvalent antiserum comprising purified and concentrated immunoglobulin G antibodies to formolized whole cells of A. israelii serotypes 1 and 2. The standard antigens provided four antigen-antibody systems for A. israelii. The immunoprecipitation patterns of the system were compared, and the immunochemical characteristics of individual precipitates were analyzed. Each system contained specific precipitates, but also one or two precipitates which were immunochemically identical to precipitates of the other systems. The standard system for A. israelii based on cytoplasmic antigens was best reproducible and revealed the highest number of immunoprecipitates. These precipitates possessed immunochemical properties which made them suitable for CIE studies. The cytoplasmic antigen mixture of A. israelii was, therefore, adopted as the most suitable for further development of a crossed immunoelectrophoretic system for A. israelii. In subsequent assays the cytoplasmic antigen mixture was raised in rabbit against cell lysates of A. israelii, serotypes 1 and 2. A standard antigen-antibody system for A. israelii was obtained which revealed an immunoprecipitation pattern of 10 distinguishable precipitates. The resolving power and separation by CIE of this standard system for A. israelii was compared with that of crossed immunoelectrofocusing. The results suggest that these methods supplement each other. Crossed immunoelectrofocusing appeared to be a useful tool for separation of specific components of the protein-antigen complex of A. israelii for analytic serology. The CIE in conjunction with a standard reference antigen-antibody system for A. israelii based on cytoplasmic antigens offers great potentialities in diagnostic A. israelii serology.
用交叉免疫电泳(CIE)分析以色列放线菌粗制细胞质和全细胞相关抗原混合物的标准制剂,所用标准多价抗血清包含针对以色列放线菌1型和2型甲醛化全细胞的纯化浓缩免疫球蛋白G抗体。这些标准抗原为以色列放线菌提供了四个抗原 - 抗体系统。比较了各系统的免疫沉淀模式,并分析了各个沉淀物的免疫化学特性。每个系统都含有特异性沉淀物,但也有一两个沉淀物在免疫化学上与其他系统的沉淀物相同。基于细胞质抗原的以色列放线菌标准系统重复性最好,显示出的免疫沉淀物数量最多。这些沉淀物具有使其适合交叉免疫电泳研究的免疫化学特性。因此,以色列放线菌的细胞质抗原混合物被认为最适合进一步开发以色列放线菌的交叉免疫电泳系统。在后续试验中,用兔针对以色列放线菌1型和2型的细胞裂解物制备细胞质抗原混合物。获得了一个以色列放线菌的标准抗原 - 抗体系统,该系统显示出由10个可区分沉淀物组成的免疫沉淀模式。将该以色列放线菌标准系统的CIE分辨能力和分离效果与交叉免疫电聚焦的进行了比较。结果表明这些方法相互补充。交叉免疫电聚焦似乎是用于分析血清学中分离以色列放线菌蛋白质 - 抗原复合物特定成分的有用工具。结合基于细胞质抗原的以色列放线菌标准参考抗原 - 抗体系统的CIE在以色列放线菌诊断血清学中具有很大潜力。