抗原
幽门螺杆菌
微生物学
抗体
免疫系统
人口
庚糖
糖复合物
脂多糖
细菌
化学
免疫学
生物
生物化学
医学
基因
突变体
环境卫生
遗传学
作者
Junchang Wang,Yiyue Zhang,Yirong Zhu,Junru Liu,Yan Chen,Xin Cao,You Yang
出处
期刊:Organic Letters
[American Chemical Society]
日期:2020-10-29
卷期号:22 (22): 8780-8785
被引量:16
标识
DOI:10.1021/acs.orglett.0c03105
摘要
Helicobacter pylori, the most common cause of chronic gastritis, peptic ulcers, and gastric cancers, infects around half of the world's population. Although the drawbacks of antibiotic-based combination therapy are emerging, no effective vaccine is available to prevent H. pylori infections. Here, we describe the total synthesis of the unique α-(1→3)-linked tri-d-glycero-d-manno-heptose antigen from the lipopolysaccharide of H. pylori serogroups O3 and O6 and strains MO19, D2, D4, and D5 based on de novo synthesis of the differentially protected d-glycero-d-manno-heptosyl building blocks. Immunization of mice with the semisynthetic glycoconjugate elicited a very robust T-cell-dependent antigen-specific immune response, resulting in very high titers of IgG1 and IgG2b protective antibody isotypes. The postimmune sera recognized H. pylori NCTC 11637 and bound strongly to the surface of the intact bacteria.
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