Kato N, Kido N, Ohta M, Naito S, Nakashima I
Microbiol Immunol. 1984;28(6):659-66. doi: 10.1111/j.1348-0421.1984.tb00720.x.
Previously we showed that Klebsiella O3 lipopolysaccharide (KO3 LPS) is much more potent than other kinds of LPS including Escherichia coli O127 LPS (EO127 LPS) in adjuvant activity in augmenting antibody response and delayed-type hypersensitivity to protein antigens and in the ability to enlarge the regional lymph node. Various defined uniform salt forms, the triethylamine, sodium, potassium, ammonium, tris(hydroxymethyl)aminomethane, and calcium salt forms, of KO3 LPS and EO127 LPS were prepared by removing basic materials present in LPS preparations by electrodialysis and neutralizing the electrodialyzed LPS preparations with various kinds of alkali. The triethylamine salt form showed the best solubility and consisted of the smallest granules and, on the other hand, the calcium salt form showed the lowest solubility, compared with the natural form and the other uniform salt forms. Even if the natural forms of KO3 LPS and EO127 LPS were converted to the defined uniform salt forms, adjuvanticity of KO3 LPS and EO127 LPS in augmenting delayed-type hypersensitivity to ovalbumin and the ability to enlarge the regional lymph node did not significantly differ from those of the respective natural forms. From these results it is concluded that the difference in strength of the adjuvanticity between KO3 LPS and EO127 LPS is not due to the difference in their salt forms, solubility or physical state. Moreover, there were no significant differences in lethal toxicity for mice by the intraperitoneal route among the natural form and all the uniform salt forms of KO3 LPS tested.
此前我们发现,克雷伯氏菌O3脂多糖(KO3 LPS)在增强抗体反应、对蛋白质抗原的迟发型超敏反应以及增大局部淋巴结的佐剂活性方面,比包括大肠杆菌O127脂多糖(EO127 LPS)在内的其他种类脂多糖要强得多。通过电渗析去除脂多糖制剂中存在的碱性物质,并用各种碱中和电渗析后的脂多糖制剂,制备了KO3 LPS和EO127 LPS的各种确定的均匀盐形式,即三乙胺盐、钠盐、钾盐、铵盐、三(羟甲基)氨基甲烷盐和钙盐形式。与天然形式和其他均匀盐形式相比,三乙胺盐形式的溶解度最佳,颗粒最小,而钙盐形式的溶解度最低。即使将KO3 LPS和EO127 LPS的天然形式转化为确定的均匀盐形式,它们在增强对卵清蛋白的迟发型超敏反应和增大局部淋巴结的佐剂活性方面,与各自的天然形式相比没有显著差异。从这些结果可以得出结论,KO3 LPS和EO127 LPS佐剂活性强度的差异不是由于它们的盐形式、溶解度或物理状态的差异。此外,在所测试的KO3 LPS的天然形式和所有均匀盐形式中,经腹腔途径对小鼠的致死毒性没有显著差异。