National Engineering Laboratory for AIDS Vaccine, School of Life Sciences, Jilin Universitygrid.64924.3d, Changchun, People's Republic of China.
QingDaogaoxin Vocational School, Qingdao, People's Republic of China.
Infect Immun. 2022 Jan 25;90(1):e0035221. doi: 10.1128/IAI.00352-21. Epub 2021 Oct 25.
Pneumococcal disease is a serious public health problem worldwide and an important cause of morbidity and mortality among children and adults in developing countries. Although vaccination is among the most effective approaches to prevent and control pneumococcal diseases, approved vaccines have limited protective effects. We developed a pneumococcal protein-polysaccharide conjugate vaccine that is mediated by the noncovalent interaction between biotin and streptavidin. Biotinylated type IV capsular polysaccharide was incubated with a fusion protein containing core streptavidin and Streptococcus pneumoniae virulence protein and relied on the noncovalent interaction between biotin and streptavidin to prepare the protein-polysaccharide conjugate vaccine. Analysis of vaccine efficacy revealed that mice immunized with the protein-polysaccharide conjugate vaccine produced antibodies with high potency against virulence proteins and polysaccharide antigens and were able to induce Th1 and Th17 responses. The antibodies identified using an opsonophagocytic assay were capable of activating the complement system and promoting pathogen elimination by phagocytes. Additionally, mice immunized with the protein-polysaccharide conjugate vaccine and then infected with a lethal dose of Streptococcus pneumoniae demonstrated induced protective immunity. The data indicated that the pneumococcal protein-polysaccharide (biotin-streptavidin) conjugate vaccine demonstrated broad-spectrum activity applicable to a wide range of people and ease of direct coupling between protein and polysaccharide. These findings provide further evidence for the application of biotin-streptavidin in S. pneumoniae vaccines.
肺炎球菌病是全球范围内一个严重的公共卫生问题,也是发展中国家儿童和成人发病率和死亡率的重要原因。尽管疫苗接种是预防和控制肺炎球菌病最有效的方法之一,但已批准的疫苗的保护效果有限。我们开发了一种肺炎球菌蛋白-多糖结合疫苗,该疫苗通过生物素和链霉亲和素之间的非共价相互作用介导。生物素化的 IV 型荚膜多糖与含有核心链霉亲和素和肺炎链球菌毒力蛋白的融合蛋白孵育,并依赖于生物素和链霉亲和素之间的非共价相互作用来制备蛋白-多糖结合疫苗。疫苗功效分析表明,用蛋白-多糖结合疫苗免疫的小鼠产生了针对毒力蛋白和多糖抗原的高效抗体,并能够诱导 Th1 和 Th17 反应。通过调理吞噬测定鉴定的抗体能够激活补体系统并促进吞噬细胞清除病原体。此外,用蛋白-多糖结合疫苗免疫然后用致死剂量的肺炎链球菌感染的小鼠表现出诱导的保护免疫。数据表明,肺炎球菌蛋白-多糖(生物素-链霉亲和素)结合疫苗具有广谱活性,适用于广泛人群,并且可以在蛋白和多糖之间直接偶联。这些发现为生物素-链霉亲和素在肺炎球菌疫苗中的应用提供了进一步的证据。