| Literature DB >> 34726473 |
David R Martinez1, Alexandra Schäfer1, Sophie Gobeil2, Dapeng Li2, Gabriela De la Cruz3, Robert Parks2, Xiaozhi Lu2, Maggie Barr2, Victoria Stalls2, Katarzyna Janowska2, Esther Beaudoin2, Kartik Manne2, Katayoun Mansouri2, Robert J Edwards2, Kenneth Cronin2, Boyd Yount1, Kara Anasti2, Stephanie A Montgomery4, Juanjie Tang5, Hana Golding5, Shaunna Shen6, Tongqing Zhou7, Peter D Kwong7, Barney S Graham7, John R Mascola7, David C Montefiori6, S Munir Alam, Gregory Sempowski2, Gregory D Sempowski2, Surender Khurana5, Kevin Wiehe2, Kevin O Saunders2,6, Priyamvada Acharya2,6, Barton F Haynes2, Ralph S Baric1.
Abstract
Severe acute respiratory syndrome coronaviruses 1 (SARS-CoV) and 2 (SARS-CoV-2), including SARS-CoV-2 variants of concern, can cause deadly infections. The mortality associated with sarbecovirus infection underscores the importance of developing broadly effective countermeasures against them, which could be key in the prevention and mitigation of current and future zoonotic events. Here, we demonstrate the neutralization of SARS-CoV; bat coronaviruses WIV-1 and RsSHC014; and SARS-CoV-2 variants D614G, B.1.1.7, B.1.351, P.1, B.1.429, B.1.526, B.1.617.1, and B.1.617.2 by a receptor binding domain (RBD)–specific human antibody, DH1047. Prophylactic and therapeutic treatment with DH1047 was protective against SARS-CoV, WIV-1, RsSHC014, and SARS-CoV-2 B.1.351 infection in mice. Binding and structural analysis showed high affinity binding of DH1047 to an epitope that is highly conserved among sarbecoviruses. Thus, DH1047 is a broadly protective antibody that can prevent infection and mitigate outbreaks caused by SARS-related strains and SARS-CoV-2 variants. Our results also suggest that the conserved RBD epitope bound by DH1047 is a rational target for a universal sarbecovirus vaccine.Entities:
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Year: 2022 PMID: 34726473 PMCID: PMC8899823 DOI: 10.1126/scitranslmed.abj7125
Source DB: PubMed Journal: Sci Transl Med ISSN: 1946-6234 Impact factor: 17.956