U.S. Air Force Epidemiological Laboratory and the Aerospace Medical Laboratory (Clinical), Lackland Air Force Base, San Antonio, Texas 78236.
Infect Immun. 1970 Jan;1(1):8-14. doi: 10.1128/iai.1.1.8-14.1970.
To prepare Neisseria meningitidis groups A, C, X, and Y polysaccharide antigens, culture supernatant fluids were subjected to serial processes of salt precipitation, alkaline hydrolysis, ethyl alcohol precipitation, and Sephadex G-200 chromatography. This method resulted in the isolation of large quantities of group antigens. All are acidic polysaccharides, the group C antigen being a polymer of n-acetyl neuraminic acid. Thiobarbituric acid assay failed to reveal sialic acids in the other group antigens. Protein was undetectable by absorption at 280 nm or by Folin analysis. These antigens are of similar molecular size, the majority of which are excluded by Sephadex G-200. They migrate in the upper one-third of sucrose density gradients and are retained by 5% acrylamide gel. All are highly group-specific and react only with homologous hyperimmune antisera in hemagglutination, complement fixation, and immunodiffusion systems. As little as 0.03 mumoles of n-acetyl neuraminic acid in group C antigen inhibits the hemagglutination of group C-sensitized red cells. All antigens are immunogenic in rabbits. These techniques afford a simplified method for the production of relatively large yields of highly specific group antigens which participate in multiple immunologic systems.
为了制备 A、C、X 和 Y 群脑膜炎奈瑟菌多糖抗原,将培养上清液进行了一系列盐沉淀、碱性水解、乙醇沉淀和 Sephadex G-200 层析处理。该方法分离出大量的组抗原。所有这些都是酸性多糖,C 组抗原是 N-乙酰神经氨酸的聚合物。硫代巴比妥酸测定未能在其他组抗原中发现唾液酸。280nm 处的吸收或福林分析未检测到蛋白质。这些抗原的分子大小相似,大多数在 Sephadex G-200 中被排除。它们在上三分之一的蔗糖密度梯度中迁移,并被 5%丙烯酰胺凝胶保留。所有抗原都具有高度的特异性,仅在血凝、补体固定和免疫扩散系统中与同源高免疫血清发生反应。C 组抗原中的 0.03 微摩尔 N-乙酰神经氨酸即可抑制 C 组致敏红细胞的凝集。所有抗原在兔子中均具有免疫原性。这些技术提供了一种简化的方法,可大量生产高度特异性的参与多种免疫系统的组抗原。