Yokochi T, Inoue Y, Miyadai T, Kimura Y, Ito H, Kato N
Department of Microbiology, Fukui Medical School.
Microbiol Immunol. 1989;33(9):747-60. doi: 10.1111/j.1348-0421.1989.tb00961.x.
Previously it was demonstrated that Klebsiella pneumoniae O3 lipopolysaccharide (KO3 LPS) exhibited much stronger adjuvant action on antibody response to subcutaneously (s.c.) injected sheep red blood cells or deaggregated bovine serum albumin than did other kinds of LPS, the R-form LPS lacking the O-specific polysaccharide chain of KO3 LPS (R-LPS), and the lipid A fractionated from KO3 LPS. We compared histological changes in the regional subcutaneous tissues of mice injected subcutaneously (s.c.) with KO3 LPS, the lipid A, and R-LPS. At the early stage after injection, KO3 LPS induced the infiltration of a large number of inflammatory cells, mainly polymorphonuclear leukocytes (PMN), at the site of injection. Neither R-LPS nor the lipid A induced the accumulation of PMN so much as KO3 LPS did. When injected s.c. with LPS from Escherichia coli O111 (EO111 LPS) and O55 (EO55 LPS), and Salmonella enteritidis (Sent LPS), the appearance of PMN at the regional site was much less than KO3 LPS. KO3 LPS could accumulate more 51Cr-labeled leukocytes at the injection site than EO111 LPS and Sent LPS. Administration of acetylsalicylic acid, which can inhibit leukocyte migration in inflammatory lesions, suppressed its adjuvant action. It was therefore suggested that the strong adjuvant action of KO3 LPS in s.c. injection might be dependent on its potent capability of accumulating PMN at the regional subcutaneous tissue. Furthermore, at the late stage after injection, the formation of several lymphoid follicles at the regional site was seen only in mice injected with KO3 LPS. It might be also related to the strong adjuvant action of KO3 LPS.
先前有研究表明,肺炎克雷伯菌O3脂多糖(KO3 LPS)对皮下注射绵羊红细胞或解聚牛血清白蛋白所引发的抗体反应表现出比其他种类脂多糖更强的佐剂作用,这些脂多糖包括缺乏KO3 LPS O特异性多糖链的R型脂多糖(R-LPS)以及从KO3 LPS中分离出的脂质A。我们比较了皮下注射KO3 LPS、脂质A和R-LPS的小鼠局部皮下组织的组织学变化。注射后早期,KO3 LPS在注射部位诱导大量炎性细胞浸润,主要是多形核白细胞(PMN)。R-LPS和脂质A均未像KO3 LPS那样诱导PMN大量聚集。当皮下注射大肠杆菌O111脂多糖(EO111 LPS)、O55脂多糖(EO55 LPS)和肠炎沙门氏菌脂多糖(Sent LPS)时,局部部位PMN的出现比KO3 LPS少得多。KO3 LPS在注射部位比EO111 LPS和Sent LPS能聚集更多的51Cr标记白细胞。给予可抑制炎性病变中白细胞迁移的乙酰水杨酸可抑制其佐剂作用。因此,提示KO3 LPS在皮下注射中的强佐剂作用可能依赖于其在局部皮下组织中聚集PMN的强大能力。此外,注射后晚期,仅在注射KO3 LPS的小鼠局部部位可见数个淋巴滤泡形成。这也可能与KO3 LPS的强佐剂作用有关。