溶血素
肺炎链球菌
免疫原性
糖复合物
微生物学
病菌
生物
血清型
免疫系统
肺炎球菌感染
免疫
抗原
肺炎球菌疫苗
免疫学
病毒学
抗生素
生物信息学
作者
Paulina Kapłonek,Ling Yao,Katrin Reppe,Franziska Voß,Thomas P. Kohler,Friederike Ebner,Alexander Schäfer,Ulrike Blohm,Patricia Priegue,Maria Bräutigam,Claney L. Pereira,Sharavathi G. Parameswarappa,Madhu Emmadi,Petra Ménová,Martin Witzenrath,Sven Hammerschmidt,Susanne Hartmann,Leif Erik Sander,Peter H. Seeberger
出处
期刊:Vaccine
[Elsevier BV]
日期:2022-02-01
卷期号:40 (7): 1038-1046
被引量:2
标识
DOI:10.1016/j.vaccine.2021.12.068
摘要
Streptococcus pneumoniae (S. pneumoniae)infections are the leading cause of child mortality globally. Currentvaccines fail to induceaprotective immune response towards a conserved part of the pathogen,resulting in newserotypescausing disease. Therefore, new vaccinestrategies are urgently needed.Described is atwo-pronged approach combiningS. pneumoniaeproteins, pneumolysin (Ply) and pneumococcal surface protein A (PspA),with aprecisely defined synthetic oligosaccharide,wherebythe carrier protein actsas a serotype-independent antigen to provideadditional protection. Proof of concept in mice and swine modelsrevealed thatthe conjugatesinhibited colonization of the nasopharynx, decreased the bacterial load and reduced disease severity in the bacteria challenge model. Immunization of piglets provided the first evidence for the immunogenicity and protective potential of synthetic glycoconjugate vaccine in a large animal model.Acombination of synthetic oligosaccharides with proteins from the target pathogen opens the path to create broadly cross-protective ("universal") pneumococcal vaccines.
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