mRNA vaccines and hybrid immunity use different B cell germlines against Omicron BA.4 and BA.5

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作者
Emanuele Andreano
Ida Paciello
Giulio Pierleoni
Giuseppe Maccari
Giada Antonelli
Valentina Abbiento
Piero Pileri
Linda Benincasa
Ginevra Giglioli
Giulia Piccini
Concetta De Santi
Claudia Sala
Duccio Medini
Emanuele Montomoli
Piet Maes
Rino Rappuoli
机构
[1] Monoclonal Antibody Discovery (MAD) Lab,Department of Molecular and Developmental Medicine
[2] Fondazione Toscana Life Sciences,KU Leuven, Rega Institute, Department of Microbiology, Immunology and Transplantation
[3] VisMederi Research S.r.l.,Department of Biotechnology, Chemistry and Pharmacy
[4] Data Science for Health (DaScH) Lab,undefined
[5] Fondazione Toscana Life Sciences,undefined
[6] VisMederi S.r.l,undefined
[7] University of Siena,undefined
[8] Laboratory of Clinical and Epidemiological Virology,undefined
[9] University of Siena,undefined
[10] Fondazione Biotecnopolo di Siena,undefined
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Severe acute respiratory syndrome 2 Omicron BA.4 and BA.5 are characterized by high transmissibility and ability to escape natural and vaccine induced immunity. Here we test the neutralizing activity of 482 human monoclonal antibodies isolated from people who received two or three mRNA vaccine doses or from people vaccinated after infection. The BA.4 and BA.5 variants are neutralized only by approximately 15% of antibodies. Remarkably, the antibodies isolated after three vaccine doses target mainly the receptor binding domain Class 1/2, while antibodies isolated after infection recognize mostly the receptor binding domain Class 3 epitope region and the N-terminal domain. Different B cell germlines are used by the analyzed cohorts. The observation that mRNA vaccination and hybrid immunity elicit a different immunity against the same antigen is intriguing and its understanding may help to design the next generation of therapeutics and vaccines against coronavirus disease 2019.
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