Immunological Exploration of Helicobacter pylori Serotype O2 O-Antigen by Using a Synthetic Glycan Library

被引:5
作者
Zhao, Ming [1 ,2 ]
Tian, Guangzong [1 ,2 ]
Qin, Chunjun [1 ,2 ]
Zou, Xiaopeng [1 ,2 ]
Seeberger, Peter H. [3 ]
Hu, Jing [4 ]
Yin, Jian [1 ,2 ]
机构
[1] Jiangnan Univ, Sch Biotechnol, Key Lab Carbohydrate Chem & Biotechnol, Minist Educ, Lihu Ave 1800, Wuxi 214122, Jiangsu, Peoples R China
[2] Jiangnan Univ, Sch Life Sciencesand Hlth Engn, Lihu Ave 1800, Wuxi 214122, Jiangsu, Peoples R China
[3] Max Planck Inst Colloids & Interfaces, Biomol Syst Dept, Muhlenberg 1, D-14476 Potsdam, Germany
[4] Jiangnan Univ, Wuxi Sch Med, Lihu Ave 1800, Wuxi 214122, Jiangsu, Peoples R China
基金
中国博士后科学基金; 中国国家自然科学基金;
关键词
Glycoconjugates; Helicobacter pylori; Immunology; Microarrays; O-antigen; Oligosaccharides; MOLECULAR RECOGNITION; VACCINE CANDIDATE; CONJUGATE VACCINE; LIPOPOLYSACCHARIDE; OLIGOSACCHARIDES; POLYSACCHARIDE; ANTIBODIES; DESIGN;
D O I
10.1002/cjoc.202300510
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Helicobacter pylori (H. pylori) infection is a threat to human health. The lipopolysaccharide (LPS) O-antigen holds promise for developing vaccines. It is meaningful to explore the immunological activity of oligosaccharides with different lengths and frameshifts for antigen development. Herein, a glycan library of H. pylori O2 O-antigen containing eight fragments is constructed. After screening with anti-H. pylori O2 LPS sera and patients' sera by glycan microarray, the disaccharide HPO2G-2b and trisaccharide HPO2G-3a show strong antigenicity and then are separately conjugated with carrier protein CRM197. Both glycoconjugates elicit a robust immunoglobulin G (IgG) immune response in rabbits. The anti-HPO2G-3a IgG antibodies possess a much stronger binding affinity with the LPS and bacteria of H. pylori O2 than the anti-HPO2G-2b IgG antibodies. There is no cross-reaction between both sera IgG antibodies with LPS and bacteria of H. pylori O1, O6, and E. coli. The results demonstrate the trisaccharide HPO2G-3a is a promising candidate for H. pylori vaccine development.
引用
收藏
页码:243 / 251
页数:9
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