Mattsby-Baltzer I, Kaijser B
Infect Immun. 1979 Mar;23(3):758-63. doi: 10.1128/iai.23.3.758-763.1979.
Lipid A in free form, in crude antigen preparations, and on Formalin-treated Escherichia coli and Salmonella minnesota R595 was employed in studies of its antigenic composition, immunogenicity, and availability on gram-negative bacteria. Analyses with immunodiffusion and crossed immunoelectrophoresis of isolated lipid A preparations revealed three components. Inhibition experiments with enzyme-linked immunosorbent assay showed that the lipid A structure was not exposed on the tested smooth or rough E. coli strains or on S. minnesota R595. In crude O antigen preparations from some of the strains, however, lipid A was available for reaction with antibodies. The inaccessibility of lipid A on the bacterial surface may explain the poor protective capacity of anti-lipid A antibodies against bacterial infections. An enzyme-linked immunosorbent assay was more sensitive for measuring anti-lipid A antibody activity than indirect hemolysis or indirect hemagglutination. With an enzyme-linked immunosorbent assay it was shown that in rabbits the immunogenicity of lipid A was approximately the same when coated on erythrocytes or, as is more commonly done, when lipid A-coated hydrolyzed bacteria were used. Some antisera from rabbits immunized with E. coli of different serotypes showed activity against lipid A, with a higher frequency for antisera from rabbits immunized with R mutants.
游离形式、粗抗原制剂中的脂多糖 A,以及经福尔马林处理的大肠杆菌和明尼苏达沙门氏菌 R595 上的脂多糖 A,被用于研究其抗原组成、免疫原性以及在革兰氏阴性菌上的可及性。对分离的脂多糖 A 制剂进行免疫扩散和交叉免疫电泳分析,发现了三种成分。酶联免疫吸附测定的抑制实验表明,脂多糖 A 结构在受试的光滑型或粗糙型大肠杆菌菌株或明尼苏达沙门氏菌 R595 上未暴露。然而,在某些菌株的粗 O 抗原制剂中,脂多糖 A 可与抗体发生反应。脂多糖 A 在细菌表面的不可及性可能解释了抗脂多糖 A 抗体对细菌感染的保护能力较差的原因。酶联免疫吸附测定在测量抗脂多糖 A 抗体活性方面比间接溶血或间接血凝更敏感。通过酶联免疫吸附测定表明,在兔子中,脂多糖 A 包被在红细胞上时,或者更常见的是使用脂多糖 A 包被的水解细菌时,其免疫原性大致相同。用不同血清型的大肠杆菌免疫兔子产生的一些抗血清显示出对脂多糖 A 的活性,用 R 突变体免疫兔子产生的抗血清活性频率更高。