Poolman J T, Hopman C T, Zanen H C
Infect Immun. 1983 Apr;40(1):398-406. doi: 10.1128/iai.40.1.398-406.1983.
The immunogenicity of meningococcal surface antigens was tested in acute- and convalescent-phase sera from patients with meningococcal diseases by enzyme-linked immunosorbent assay and gel immunoradioassay. In gel immunoradioassay, the antigens are separated by sodium dodecyl sulfate-polyacrylamide gel electrophoresis before testing their antibody-binding capacity. Both 125I-labeled protein A and 125I-labeled anti-human immunoglobulin G were used to detect antibody binding. It appeared that the variable, low-molecular-weight, heat-modifiable major outer membrane proteins (molecular weights, 25,000 to 32,000) induced strong, strain-specific immunoglobulin G antibody responses. In addition, pili induced strong, cross-reactive antibody responses that could be detected with 125I-labeled protein A, but not with 125I-labeled anti-immunoglobulin G. Antibody responses against capsular polysaccharides, lipopolysaccharides, and minor outer membrane proteins could also be detected by gel immunoradioassay. When tested by enzyme-linked immunosorbent assay against outer membrane complexes, patient sera demonstrated a large amount of cross-reactivity against heterologous meningococcal strains.
通过酶联免疫吸附测定法和凝胶免疫放射测定法,对脑膜炎球菌病患者急性期和恢复期血清中的脑膜炎球菌表面抗原免疫原性进行了检测。在凝胶免疫放射测定法中,抗原在检测其抗体结合能力之前,先通过十二烷基硫酸钠-聚丙烯酰胺凝胶电泳进行分离。125I标记的蛋白A和125I标记的抗人免疫球蛋白G均用于检测抗体结合。结果显示,可变的、低分子量的、热可修饰的主要外膜蛋白(分子量为25,000至32,000)可诱导强烈的、菌株特异性的免疫球蛋白G抗体反应。此外,菌毛可诱导强烈的交叉反应性抗体反应,可用125I标记的蛋白A检测到,但不能用125I标记的抗免疫球蛋白G检测到。通过凝胶免疫放射测定法也可检测到针对荚膜多糖、脂多糖和次要外膜蛋白的抗体反应。当用酶联免疫吸附测定法检测外膜复合物时,患者血清显示出对异源脑膜炎球菌菌株的大量交叉反应性。