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B cell analyses after SARS-CoV-2 mRNA third vaccination reveals a hybrid immunity like antibody response

Author

Listed:
  • Emanuele Andreano

    (Fondazione Toscana Life Sciences)

  • Ida Paciello

    (Fondazione Toscana Life Sciences)

  • Giulio Pierleoni

    (VisMederi Research S.r.l.)

  • Giulia Piccini

    (VisMederi S.r.l)

  • Valentina Abbiento

    (Fondazione Toscana Life Sciences)

  • Giada Antonelli

    (Fondazione Toscana Life Sciences)

  • Piero Pileri

    (Fondazione Toscana Life Sciences)

  • Noemi Manganaro

    (Fondazione Toscana Life Sciences)

  • Elisa Pantano

    (Fondazione Toscana Life Sciences)

  • Giuseppe Maccari

    (Fondazione Toscana Life Sciences)

  • Silvia Marchese

    (University of Milan)

  • Lorena Donnici

    (INGM, Istituto Nazionale Genetica Molecolare “Romeo ed Enrica Invernizzi”)

  • Linda Benincasa

    (VisMederi Research S.r.l.)

  • Ginevra Giglioli

    (VisMederi Research S.r.l.)

  • Margherita Leonardi

    (VisMederi Research S.r.l.
    VisMederi S.r.l)

  • Concetta De Santi

    (Fondazione Toscana Life Sciences)

  • Massimiliano Fabbiani

    (Siena University Hospital)

  • Ilaria Rancan

    (Siena University Hospital)

  • Mario Tumbarello

    (Siena University Hospital
    University of Siena)

  • Francesca Montagnani

    (Siena University Hospital
    University of Siena)

  • Claudia Sala

    (Fondazione Toscana Life Sciences)

  • Duccio Medini

    (Fondazione Toscana Life Sciences)

  • Raffaele De Francesco

    (University of Milan
    INGM, Istituto Nazionale Genetica Molecolare “Romeo ed Enrica Invernizzi”)

  • Emanuele Montomoli

    (VisMederi Research S.r.l.
    VisMederi S.r.l
    University of Siena)

  • Rino Rappuoli

    (Fondazione Toscana Life Sciences
    University of Siena)

Abstract

The continuous evolution of SARS-CoV-2 generated highly mutated variants able to escape natural and vaccine-induced primary immunity. The administration of a third mRNA vaccine dose induces a secondary response with increased protection. Here we investigate the longitudinal evolution of the neutralizing antibody response in four donors after three mRNA doses at single-cell level. We sorted 4100 spike protein specific memory B cells identifying 350 neutralizing antibodies. The third dose increases the antibody neutralization potency and breadth against all SARS-CoV-2 variants as observed with hybrid immunity. However, the B cell repertoire generating this response is different. The increases of neutralizing antibody responses is largely due to the expansion of B cell germlines poorly represented after two doses, and the reduction of germlines predominant after primary immunization. Our data show that different immunization regimens induce specific molecular signatures which should be considered while designing new vaccines and immunization strategies.

Suggested Citation

  • Emanuele Andreano & Ida Paciello & Giulio Pierleoni & Giulia Piccini & Valentina Abbiento & Giada Antonelli & Piero Pileri & Noemi Manganaro & Elisa Pantano & Giuseppe Maccari & Silvia Marchese & Lore, 2023. "B cell analyses after SARS-CoV-2 mRNA third vaccination reveals a hybrid immunity like antibody response," Nature Communications, Nature, vol. 14(1), pages 1-9, December.
  • Handle: RePEc:nat:natcom:v:14:y:2023:i:1:d:10.1038_s41467-022-35781-6
    DOI: 10.1038/s41467-022-35781-6
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    1. Emanuele Andreano & Ida Paciello & Giulia Piccini & Noemi Manganaro & Piero Pileri & Inesa Hyseni & Margherita Leonardi & Elisa Pantano & Valentina Abbiento & Linda Benincasa & Ginevra Giglioli & Conc, 2021. "Hybrid immunity improves B cells and antibodies against SARS-CoV-2 variants," Nature, Nature, vol. 600(7889), pages 530-535, December.
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    1. Emanuele Andreano & Ida Paciello & Giulio Pierleoni & Giuseppe Maccari & Giada Antonelli & Valentina Abbiento & Piero Pileri & Linda Benincasa & Ginevra Giglioli & Giulia Piccini & Concetta De Santi &, 2023. "mRNA vaccines and hybrid immunity use different B cell germlines against Omicron BA.4 and BA.5," Nature Communications, Nature, vol. 14(1), pages 1-9, December.

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