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Immunogenicity evaluation of semisynthetic α-(1 → 3)-D,D-heptoglycan conjugates for Helicobacter pylori vaccine
Xiaopeng Zou1, Lei Xiao2, Guangzong Tian1
1School of Biotechnology and Key Laboratory of Carbohydrate Chemistry and Biotechnology of Ministry of Education, Jiangnan University, Lihu Ave. 1800, Wuxi, 214122, China; Innovation Center for Vaccine Engineering, Jiangnan University, Lihu Ave. 1800, Wuxi, 214122, China.
Abstract:
Helicobacter pylori is a Gram-negative bacterium that infects nearly half the global population and is associated with a range of gastric diseases, including gastric cancer. The lipopolysaccharides on the surface of H. pylori are immunogenic and have been regarded as attractive targets for carbohydrate-based vaccines. In this study, two semisynthetic glycoconjugates, CRM197-1 and CRM197-4, were prepared by conjugating a α-(1 → 3)-D,D-hepto-disaccharide and a α-(1 → 3)-D,D-hepto-pentasaccharide, respectively, with carrier protein CRM197. Compared with CRM197-1, CRM197-4 elicited a more robust antigen-specific IgG response in rabbits and exhibited stronger binding affinities to synthetic heptoglycans. Moreover, sera from rabbits immunized with CRM197-4 showed pronounced recognition of native O6 H. pylori LPS in microarray analysis. These findings identify CRM197-4, featuring a longer heptoglycan chain, as a promising candidate for further development of heptoglycan-conjugate vaccines against H. pylori infection.
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