Development and usefulness of the gelatin-particle-agglutination test for titration of antibodies against diphtheria, pertussis and tetanus toxins.

K Miyamura, S Sadahiro, T Konda, M Takahashi, R Fujino, Y Nishimura, H Miyakoshi, K Horiuchi, Y Furuya, T Kubota
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引用次数: 5

Abstract

The gelatin-particle-agglutination (PA) test for titrating antibodies against diphtheria, pertussis and tetanus toxins was developed and used for assaying 65 sera from healthy children to assess the antitoxin acquisition in relation to the administration of adsorbed diphtheria-purified pertussis-tetanus (DPT) combined vaccine. The antitoxin titers obtained by the PA test and the conventional methods were correlated well; the correlation coefficient of the diphtheria antitoxin titers between the PA test and the cell culture method was 0.908, that of the tetanus antitoxin titers between the PA test and the passive hemagglutination test 0.968, and that of anti-pertussis toxin titers between the PA test and polystyrene-ball ELISA 0.885. The PA test was shown to be useful in both developed and developing countries, since it is simple to perform, sensitive and specific, and the three antitoxins can be titrated by the same procedure.

明胶颗粒凝集试验测定白喉、百日咳和破伤风毒素抗体的发展和用途。
开发了用于测定白喉、百日咳和破伤风毒素抗体的明胶颗粒凝集(PA)试验,并用于测定65份健康儿童血清,以评估与吸附白喉-纯化百日咳-破伤风(DPT)联合疫苗接种有关的抗毒素获得。PA试验所得抗毒素效价与常规方法相关性较好;白喉抗毒素滴度与细胞培养法的相关系数为0.908,破伤风抗毒素滴度与被动血凝试验的相关系数为0.968,百日咳抗毒素滴度与聚苯乙胺球ELISA的相关系数为0.885。PA试验在发达国家和发展中国家都被证明是有用的,因为它操作简单、敏感和特异,而且三种抗毒素可以用相同的程序滴定。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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