肺炎链球菌
免疫原性
四糖
血清型
聚糖
多糖
微生物学
结合疫苗
抗原
生物
抗体
肺炎球菌感染
病毒学
免疫学
抗生素
生物化学
糖蛋白
作者
M. Ravinder,Yu‐Hsuan Lih,Hanmanth Reddy Vulupala,Chiang-Yun Chen,Mei‐Hua Hsu,H. Christine Lo,Kuo‐Shiang Liao,Yang‐Yu Cheng,Cheng‐Hsun Chiu,Chung‐Yi Wu
标识
DOI:10.1021/acsinfecdis.1c00646
摘要
Streptococcus pneumoniae serotypes 6A and 6B are two of the common causes of invasive pneumococcal diseases. Although capsular polysaccharide conjugates of these two serotypes are included in the leading 13-valent pneumococcal conjugate vaccine, its low immunogenicity and high threshold for manufacturing technology indicated the need for vaccine improvement. Structurally defined synthetic immunogens have potential in dealing with these problems. To this end, we built a library of capsular polysaccharide fragments through convergent chemical synthesis in [2 + 2], [4 + 4], [4 + 3], [4 + 2], and [4 + 1] coupling manners. The library is comprised of 18 glycan antigens from trisaccharides to pseudo-octasaccharides, derived from the capsular repeating phosphorylated pseudo-tetrasaccharide with or without phosphate. Eight of them were selected for mouse immunization and further immunological studies. Four pseudo-tetrasaccharides with terminal or bridging phosphate elicited opsonic antibodies, which exhibited bactericidal activities and moderate cross-reactivities.
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