Vistnes A I, Rosenqvist E, Frøholm L O
J Clin Microbiol. 1983 Oct;18(4):905-11. doi: 10.1128/jcm.18.4.905-911.1983.
A modified and improved spin membrane immunoassay has been developed for detecting complement-activating antibodies to Neisseria meningitidis capsular polysaccharide antigens. The polysaccharides were incorporated in the membranes of large unilamellar vesicles prepared by the reverse-phase evaporation method and filled with the water-soluble spin label tempocholine chloride. Upon addition of group-specific antisera and complement, the lipid membrane was damaged and the spin label leaked out. This process was monitored by electron spin resonance spectroscopy. A satisfactory assay was developed for polysaccharides of group A and C, whereas in the case of the B system the assay was more labile. The method is rapid and has a sensitivity comparable to that of radioimmunoassay. When studying paired sera from five recruits vaccinated with an A + C polysaccharide vaccine, significant rises in titers to both A and C polysaccharides were observed in all the postvaccination sera.
已开发出一种改良和改进的自旋膜免疫测定法,用于检测针对脑膜炎奈瑟菌荚膜多糖抗原的补体激活抗体。多糖被掺入通过反相蒸发法制备的大单层囊泡的膜中,并填充有水溶性自旋标记氯化坦波胆碱。加入组特异性抗血清和补体后,脂质膜受损,自旋标记泄漏出来。通过电子自旋共振光谱监测这一过程。针对A组和C组多糖开发出了令人满意的测定法,而在B组系统中,该测定法更不稳定。该方法快速,灵敏度与放射免疫测定法相当。在研究五名接种A + C多糖疫苗的新兵的配对血清时,在所有接种后血清中均观察到A组和C组多糖的滴度显著升高。