| Literature DB >> 35654851 |
Wan-Ting He1,2,3, Rami Musharrafieh1,2,3, Ge Song1,2,3, Katharina Dueker1,2,3, Longping V Tse4, David R Martinez4, Alexandra Schäfer4, Sean Callaghan1,2,3, Peter Yong1,2,3, Nathan Beutler1, Jonathan L Torres5, Reid M Volk5, Panpan Zhou1,2,3, Meng Yuan5, Hejun Liu5, Fabio Anzanello1,2,3, Tazio Capozzola1,2,3, Mara Parren1, Elijah Garcia1, Stephen A Rawlings6, Davey M Smith6, Ian A Wilson2,3,5,7, Yana Safonova8, Andrew B Ward2,3,5, Thomas F Rogers1,6, Ralph S Baric9,10, Lisa E Gralinski11, Dennis R Burton12,13,14,15, Raiees Andrabi16,17,18.
Abstract
The emergence of current severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) variants of concern (VOCs) and potential future spillovers of SARS-like coronaviruses into humans pose a major threat to human health and the global economy. Development of broadly effective coronavirus vaccines that can mitigate these threats is needed. Here, we utilized a targeted donor selection strategy to isolate a large panel of human broadly neutralizing antibodies (bnAbs) to sarbecoviruses. Many of these bnAbs are remarkably effective in neutralizing a diversity of sarbecoviruses and against most SARS-CoV-2 VOCs, including the Omicron variant. Neutralization breadth is achieved by bnAb binding to epitopes on a relatively conserved face of the receptor-binding domain (RBD). Consistent with targeting of conserved sites, select RBD bnAbs exhibited protective efficacy against diverse SARS-like coronaviruses in a prophylaxis challenge model in vivo. These bnAbs provide new opportunities and choices for next-generation antibody prophylactic and therapeutic applications and provide a molecular basis for effective design of pan-sarbecovirus vaccines.Entities:
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Year: 2022 PMID: 35654851 DOI: 10.1038/s41590-022-01222-1
Source DB: PubMed Journal: Nat Immunol ISSN: 1529-2908 Impact factor: 31.250