Broadly neutralizing anti-S2 antibodies protect against all three human betacoronaviruses that cause severe disease
P. Zhou, G. Song, W.-t. He, N. Beutler, L. V. Tse, D. R. Martinez, A. Schafer, F. Anzanello, P. Yong, L. Peng, K. Dueker, R. Musharrafieh, S. Callaghan, T. Capozzola, M. Yuan, H. Liu, O. Limbo, M. Parren, E. Garcia, S. A. Rawlings, D. M. Smith, D. Nemazee, J. G. Jardine, I. A. Wilson, Y. Safonova, , R. Andrabi
Abstract
Pan-betacoronavirus neutralizing antibodies may hold the key to developing broadly protective vaccines against coronaviruses that cause severe disease, for anticipating novel pandemic-causing viruses, and to respond more effectively to SARS-CoV-2 variants. The emergence of the Omicron variant of SARS-CoV-2 has illustrated the limitations of solely targeting the receptor binding domain (RBD) of the envelope Spike (S)-protein. Here, we isolated a large panel of broadly neutralizing antibodies (bnAbs) from SARS-CoV-2 recovered-vaccinated donors that target a conserved S2 region in the fusion machinery on betacoronavirus spikes. Select bnAbs show broad in vivo protection against all three pathogenic betacoronaviruses, SARS-CoV-1, SARS-CoV-2 and MERS-CoV, that have spilled over into humans in the past 20 years to cause severe disease. The bnAbs provide new opportunities for antibody-based interventions and key insights for developing pan-betacoronavirus vaccines.
02 /Specification & Classification
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