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    A semisynthetic glycoconjugate provides expanded cross-serotype protection against Streptococcus pneumoniae (2022)

    Art
    Zeitschriftenartikel / wissenschaftlicher Beitrag
    Autoren
    Kaplonek, Paulina
    Yao, Ling
    Reppe, Katrin
    Voß, Franziska
    Kohler, Thomas
    Ebner, Friederike (WE 6)
    Schäfer, Alexander
    Blohm, Ulrike
    Priegue, Patricia
    Bräutigam, Maria
    Pereira, Claney L.
    Parameswarappa, Sharavathi G.
    Emmadi, Madhu
    Ménová, Petra
    Witzenrath, Martin
    Hammerschmidt, Sven
    Hartmann, Susanne (WE 6)
    Sander, Leif E.
    Seeberger, Peter H.
    Quelle
    Vaccine
    Bandzählung: 40
    Heftzählung: 7
    Seiten: 1038 – 1046
    ISSN: 0264-410x
    Sprache
    Englisch
    Verweise
    URL (Volltext): https://www.sciencedirect.com/science/article/pii/S0264410X21016765
    DOI: 10.1016/j.vaccine.2021.12.068
    Pubmed: 35033388
    Kontakt
    Institut für Immunologie

    Robert-von-Ostertag-Str. 7-13
    14163 Berlin
    +49 30 838 51834
    immunologie@vetmed.fu-berlin.de

    Abstract / Zusammenfassung

    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.