Department of Chemistry, Graduate School of Science, Osaka University, 1-1 Machikaneyama Toyonaka, Osaka 560-0043, Japan.
Carbohydr Res. 2012 Jul 15;356:37-43. doi: 10.1016/j.carres.2012.03.013. Epub 2012 Mar 23.
Helicobacter pylori, a Gram-negative bacterium, causes gastroduodenal inflammatory diseases such as chronic gastritis and peptic ulcers, and is also a risk factor for gastric carcinogenesis. In this article, we review recent developments and findings in the chemical synthesis and immunomodulatory activities of H. pylori lipid A and 3-deoxy-D-manno-2-octulosonic acid (Kdo)-lipid A, to clarify the structural basis for the inflammatory response to H. pylori LPS. The synthetic methods include a new divergent synthetic approach with a widely applicable key intermediate for other types of lipid A structures, as well as a selective α-glycosylation reaction between Kdo and lipid A. Cytokine induction assays of the chemically synthesized lipid A structures showed selective cytokine induction depending on the patterns of acyl groups and phosphate groups. The results of cytokine induction assay suggested that H. pylori LPS can modulate the immune response during infection, and also plays a role in chronic inflammatory responses.
幽门螺杆菌是一种革兰氏阴性细菌,可引起胃十二指肠炎症性疾病,如慢性胃炎和消化性溃疡,也是胃癌发生的危险因素。在本文中,我们综述了幽门螺杆菌脂多糖(LPS)化学合成及其免疫调节活性的最新研究进展,以阐明对幽门螺杆菌 LPS 炎症反应的结构基础。合成方法包括一种新的发散合成方法,具有广泛适用于其他类型 LPS 结构的关键中间体,以及 Kdo 与 LPS 之间的选择性α-糖苷化反应。化学合成 LPS 结构的细胞因子诱导实验表明,根据酰基和磷酸基团的模式,可选择性诱导细胞因子。细胞因子诱导实验的结果表明,幽门螺杆菌 LPS 可在感染过程中调节免疫反应,并在慢性炎症反应中发挥作用。