Safety, reactogenicity, and immunogenicity of homologous and heterologous prime-boost immunisation with ChAdOx1-nCoV19 and BNT162b2: a prospective cohort study

David Hillus(Humboldt-Universität zu Berlin), Tatjana Schwarz(Humboldt-Universität zu Berlin), Pinkus Tober‐Lau(Humboldt-Universität zu Berlin), Hana Hastor(Humboldt-Universität zu Berlin), Charlotte Thibeault(Humboldt-Universität zu Berlin), Stefanie Kasper(Humboldt-Universität zu Berlin), Elisa T. Helbig(Humboldt-Universität zu Berlin), Lena J. Lippert(Humboldt-Universität zu Berlin), Patricia Tscheak(Humboldt-Universität zu Berlin), Marie Luisa Schmidt(Humboldt-Universität zu Berlin), Johanna Riege(Humboldt-Universität zu Berlin), André Solarek(Humboldt-Universität zu Berlin), Christof von Kalle(Humboldt-Universität zu Berlin), Chantip Dang‐Heine(Humboldt-Universität zu Berlin), Piotr Kopankiewicz(Humboldt-Universität zu Berlin), Norbert Suttorp(Humboldt-Universität zu Berlin), Christian Drosten(Humboldt-Universität zu Berlin), Harald Bias(Humboldt-Universität zu Berlin), Joachim Seybold(Humboldt-Universität zu Berlin), EICOV/COVIM Study Group(Humboldt-Universität zu Berlin), Claudia Conrad(Humboldt-Universität zu Berlin), Doris Steuer(Humboldt-Universität zu Berlin), U. Glaser(Humboldt-Universität zu Berlin), Anne-Sophie Sinnigen(Humboldt-Universität zu Berlin), Carolin Rubisch(Humboldt-Universität zu Berlin), Nadine Olk(Humboldt-Universität zu Berlin), Lisbeth Hasler(Humboldt-Universität zu Berlin), Angela Sanchez-Rezza(Humboldt-Universität zu Berlin), Paolo Kronenberg(Humboldt-Universität zu Berlin), Alexandra Horn(Humboldt-Universität zu Berlin), Willi Koch(Humboldt-Universität zu Berlin), Paula Stubbemann(Humboldt-Universität zu Berlin), Julie-Anne Gabelich(Humboldt-Universität zu Berlin), Friederike Münn(Humboldt-Universität zu Berlin), Julia Tesch(Humboldt-Universität zu Berlin), Petra Mackeldanz(Humboldt-Universität zu Berlin), Léon Bergfeld(Humboldt-Universität zu Berlin), Tobias Bleicker(Humboldt-Universität zu Berlin), Jörn Beheim-Schwarzbach(Humboldt-Universität zu Berlin), Anna Hiller(Humboldt-Universität zu Berlin), Sophia Brumhard(Humboldt-Universität zu Berlin), Lara Bardtke(Humboldt-Universität zu Berlin), Kai Pohl(Humboldt-Universität zu Berlin), Daniel Wendisch(Humboldt-Universität zu Berlin), Philipp Georg(Humboldt-Universität zu Berlin), Denise Treue(Humboldt-Universität zu Berlin), Dana Briesemeister(Humboldt-Universität zu Berlin), Jenny Schlesinger(Humboldt-Universität zu Berlin), Andreas Hetey(Humboldt-Universität zu Berlin), Luisa Kegel(Humboldt-Universität zu Berlin), Annelie Richter(Humboldt-Universität zu Berlin), Ben Al-Rim(Humboldt-Universität zu Berlin), Birgit Maeß(Humboldt-Universität zu Berlin), Kerstin Behn(Humboldt-Universität zu Berlin), Michelle Lysi(Humboldt-Universität zu Berlin), Saskia Zvorc(Humboldt-Universität zu Berlin), Maria Rönnefarth(Humboldt-Universität zu Berlin), Sein Schmidt(Humboldt-Universität zu Berlin), Alexander Krannich(Humboldt-Universität zu Berlin), Isabelle Schellenberger(Humboldt-Universität zu Berlin), Georg Schwanitz(Humboldt-Universität zu Berlin), Viktoria Schenkel(Humboldt-Universität zu Berlin), Norma Bethke(Humboldt-Universität zu Berlin), Claudia Hülso(Humboldt-Universität zu Berlin), Sebastian Dieckmann(Humboldt-Universität zu Berlin), Christian Peiser(Universität Hamburg), Florian Kurth(Universität Hamburg), Victor M. Corman(Humboldt-Universität zu Berlin), Leif Erik Sander(Humboldt-Universität zu Berlin)
medRxiv
May 22, 2021
Cited by 73Open Access
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Abstract

Abstract Objective to assess reactogenicity and immunogenicity of heterologous prime-boost immunisations of ChAdOx1-nCoV19 (Vaxzevria, ChAdOx) followed by BNT162b2 (Comirnaty, BNT) compared to homologous BNT/BNT immunisation. Design prospective, observational cohort study. Setting unicenter study in a cohort of health care workers at a tertiary care center in Berlin, Germany. Participants 340 health care workers immunised between 27 December 2020 and 21 May 2021 at Charité - Universitätsmedizin Berlin, Germany Main outcome measures the main outcomes were reactogenicity assessed on days one, three, five and seven post prime and boost vaccination, and immunogenicity measured by serum SARS-CoV-2 full spike-, spike S1-, and spike RBD-IgG, virus neutralisation capacity, anti-S1-IgG avidity, and T cell reactivity measured by Interferon gamma release assay at 3-4 weeks post prime and boost immunisation. Results Heterologous ChAdOx/BNT booster vaccination was overall well-tolerated and reactogenicity was largely comparable to homologous BNT/BNT vaccination. Systemic reactions were most frequent after prime immunisation with ChAdOx (86%, 95CI: 79-91), and less frequent after homologous BNT/BNT (65%, 95CI: 56-72), or heterologous ChAdOx/BNT booster vaccination (48%, 95CI: 36-59). Serum antibody responses and T cell reactivity were strongly increased after both homologous and heterologous boost, and immunogenicity was overall robust, and comparable between both regimens in this cohort, with slightly increased S1-IgG avidity and T cell responses following heterologous booster immunisation. Conclusions Evidence of rare thrombotic events associated with ChAdOx has led to recommendation of a heterologous booster with mRNA vaccines for certain age groups in several European countries, despite a lack of robust safety and immunogenicity data for this vaccine regimen. This interim analysis provides evidence that the currently recommended heterologous ChAdOx/BNT immunisation regimen with 10-12 week vaccine intervals is well tolerated and slightly more immunogenic compared to homologous BNT/BNT vaccination with three week vaccine intervals. Heterologous prime-boost immunisation for COVID-19 may be generally applicable to optimise logistics and improve immunogenicity and to mitigate potential intermittent supply shortages for individual vaccines.


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