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Isolation and Characterization of Cross-Neutralizing Coronavirus Antibodies from COVID-19+ Subjects

Jennewein, M.; MacCamey, A.; Akins, N.; Feng, J.; Homad, L.; Hurlburt, N.; Seydoux, E.; Wang, Y.-H.; Stuart, A. B.; Edara, V. V.; Floyd, K.; Vanderheiden, A.; Mascola, J. R.; Doria-Rose, N.; Wang, L.; Yang, E.; Chu, H.; Torres, J.; Ozorowski, G.; Ward, A.; Whaley, R.; Cohen, K.; Pancera, M.; McElrath, J.; Englund, J. A.; Finzi, A.; Suthar, M.; McGuire, A.; Stamatatos, L.

2021-03-24 immunology
10.1101/2021.03.23.436684 bioRxiv
Show abstract

SARS-CoV-2 is one of three coronaviruses that have crossed the animal-to-human barrier in the past two decades. The development of a universal human coronavirus vaccine could prevent future pandemics. We characterized 198 antibodies isolated from four COVID19+ subjects and identified 14 SARS-CoV-2 neutralizing antibodies. One targeted the NTD, one recognized an epitope in S2 and twelve bound the RBD. Three anti-RBD neutralizing antibodies cross-neutralized SARS-CoV-1 by effectively blocking binding of both the SARS-CoV-1 and SARS-CoV-2 RBDs to the ACE2 receptor. Using the K18-hACE transgenic mouse model, we demonstrate that the neutralization potency rather than the antibody epitope specificity regulates the in vivo protective potential of anti-SARS-CoV-2 antibodies. The anti-S2 antibody also neutralized SARS-CoV-1 and all four cross-neutralizing antibodies neutralized the B.1.351 mutant strain. Thus, our study reveals that epitopes in S2 can serve as blueprints for the design of immunogens capable of eliciting cross-neutralizing coronavirus antibodies.

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