Kato N, Kido N, Ohta M, Naito S
Immunology. 1985 Feb;54(2):317-24.
Previously, we found that Klebsiella O3 lipopolysaccharide (KO3 LPS) exhibits very strong adjuvant activity in augmenting the delayed-type hypersensitivity and antibody responses to protein antigens, and also strong ability to enlarge the regional lymph node in mice. By hydrolysis in 1% acetic acid at 100 degrees for 1 hr, KO3 LPS was dissociated into 54-60% polysaccharide fraction and 25-27% lipid A fraction. The lipid A fraction thus prepared retained lethal toxicity for mice, whereas the polysaccharide fraction was essentially non-toxic. However, neither the lipid A fraction nor the polysaccharide fraction could reproduce the strong adjuvanticity of KO3 LPS, and a simple mixture of these two fractions also failed to do so. It is therefore concluded that, for expression of the strong adjuvanticity of KO3 LPS, both the lipid A and polysaccharide moieties are indispensable and must be combined in the form of LPS. By contrast, administration of relatively large amounts of the lipid A fraction alone could elicit enlargement of the regional lymph node to the same degree as that attained by KO3 LPS. The regional lymph node-enlarging activity of the lipid A fraction in lesser amounts was enhanced by addition of the polysaccharide fraction. It is therefore likely that there is no direct correlation between adjuvant activity of the LPS or its derivatives, and their regional lymph node-enlarging activity.
此前,我们发现肺炎克雷伯菌O3脂多糖(KO3 LPS)在增强对蛋白质抗原的迟发型超敏反应和抗体反应方面表现出非常强的佐剂活性,并且在扩大小鼠局部淋巴结方面也有很强的能力。通过在100℃下于1%乙酸中水解1小时,KO3 LPS被解离为54 - 60%的多糖部分和25 - 27%的脂多糖A部分。如此制备的脂多糖A部分对小鼠仍保留致死毒性,而多糖部分基本无毒。然而,脂多糖A部分和多糖部分均无法重现KO3 LPS的强佐剂活性,且这两个部分的简单混合物也无法做到。因此得出结论,对于KO3 LPS强佐剂活性的表达,脂多糖A部分和多糖部分都是不可或缺的,并且必须以脂多糖的形式结合。相比之下,单独给予相对大量的脂多糖A部分可引起局部淋巴结肿大至与KO3 LPS相同的程度。少量脂多糖A部分的局部淋巴结肿大活性通过添加多糖部分而增强。因此,脂多糖或其衍生物的佐剂活性与其局部淋巴结肿大活性之间可能没有直接关联。