Da Costa Castro J M, Deschamps F, Benbachir M, Henrichsen J, Volle P J, Guinet R M
Centre d'Immunochimie Microbienne, Institut Pasteur, Lyon, France.
J Immunol Methods. 1987 Nov 23;104(1-2):265-70. doi: 10.1016/0022-1759(87)90514-x.
The immunological detection of soluble pneumococcal polysaccharide antigens in pathological products is of importance in the direct diagnosis of meningitis or pulmonary infections. We have developed a double antibody sandwich ELISA method using a biotin-avidin system using antibodies constituted with a mixture of IgGs from pooled and/or monospecific antipneumococcal sera provided by the Danish Statens Seruminstitut. The sensitivity of this rapid ELISA method was optimized with purified capsular polysaccharides of the 24 main pneumococcal serotypes. With incubation steps of 30 min at 37 degrees C for the antigens and the conjugates, the detection limit was close to 1 ng/ml for 75% of the purified polysaccharides. A retrospective study of 46 CSF samples established the validity of the assay. This type of modified ELISA system represents a specific, sensitive and rapid procedure for the potential detection of capsular soluble antigens of all pneumococcal serotypes.
在病理产物中对可溶性肺炎球菌多糖抗原进行免疫检测,对于脑膜炎或肺部感染的直接诊断具有重要意义。我们利用丹麦国家血清研究所提供的混合和/或单特异性抗肺炎球菌血清的IgG混合物构成的抗体,开发了一种使用生物素-抗生物素蛋白系统的双抗体夹心ELISA方法。该快速ELISA方法的灵敏度通过24种主要肺炎球菌血清型的纯化荚膜多糖进行了优化。抗原和结合物在37℃孵育30分钟,75%的纯化多糖的检测限接近1 ng/ml。对46份脑脊液样本的回顾性研究证实了该检测方法的有效性。这种改良的ELISA系统代表了一种用于潜在检测所有肺炎球菌血清型荚膜可溶性抗原的特异性、灵敏且快速的方法。