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    Live-attenuated vaccine sCPD9 elicits superior mucosal and systemic immunity to SARS-CoV-2 variants in hamsters (2023)

    Art
    Zeitschriftenartikel / wissenschaftlicher Beitrag
    Autoren
    Nouailles, Geraldine
    Adler, Julia M. (WE 5)
    Pennitz, Peter
    Peidli, Stefan
    Teixeira Alves, Luiz Gustavo
    Baumgardt, Morris
    Bushe, Judith (WE 12)
    Voss, Anne (WE 12)
    Langenhagen, Alina (WE 12)
    Langner, Christine (WE 5)
    Martin Vidal, Ricardo (WE 5)
    Pott, Fabian
    Kazmierski, Julia
    Ebenig, Aileen
    Lange, Mona V.
    Mühlebach, Michael D.
    Goekeri, Cengiz
    Simmons, Szandor
    Xing, Na (WE 5)
    Abdelgawad, Azza (WE 5)
    Herwig, Susanne
    Cichon, Günter
    Niemeyer, Daniela
    Drosten, Christian
    Goffinet, Christine
    Landthaler, Markus
    Blüthgen, Nils
    Wu, Haibo
    Witzenrath, Martin
    Gruber, Achim D. (WE 12)
    Praktiknjo, Samantha D.
    Osterrieder, Nikolaus (WE 5)
    Wyler, Emanuel
    Kunec, Dusan (WE 5)
    Trimpert, Jakob (WE 5)
    Quelle
    Nature microbiology
    Bandzählung: 8
    Heftzählung: 5
    Seiten: 860 – 874
    ISSN: 2058-5276
    Sprache
    Englisch
    Verweise
    URL (Volltext): https://www.nature.com/articles/s41564-023-01352-8
    DOI: 10.1038/s41564-023-01352-8
    Pubmed: 37012419
    Kontakt
    Institut für Virologie

    Robert-von-Ostertag-Str. 7-13
    14163 Berlin
    +49 30 838 51833
    virologie@vetmed.fu-berlin.de

    Abstract / Zusammenfassung

    Vaccines play a critical role in combating the COVID-19 pandemic. Future control of the pandemic requires improved vaccines with high efficacy against newly emerging SARS-CoV-2 variants and the ability to reduce virus transmission. Here we compare immune responses and preclinical efficacy of the mRNA vaccine BNT162b2, the adenovirus-vectored spike vaccine Ad2-spike and the live-attenuated virus vaccine candidate sCPD9 in Syrian hamsters, using both homogeneous and heterologous vaccination regimens. Comparative vaccine efficacy was assessed by employing readouts from virus titrations to single-cell RNA sequencing. Our results show that sCPD9 vaccination elicited the most robust immunity, including rapid viral clearance, reduced tissue damage, fast differentiation of pre-plasmablasts, strong systemic and mucosal humoral responses, and rapid recall of memory T cells from lung tissue after challenge with heterologous SARS-CoV-2. Overall, our results demonstrate that live-attenuated vaccines offer advantages over currently available COVID-19 vaccines.