| Literature DB >> 33306954 |
Jinhui Dong1, Robert W Cross2, Michael P Doyle3, Nurgun Kose1, Jarrod J Mousa1, Edward J Annand4, Viktoriya Borisevich2, Krystle N Agans2, Rachel Sutton1, Rachel Nargi1, Mahsa Majedi1, Karla A Fenton2, Walter Reichard1, Robin G Bombardi1, Thomas W Geisbert2, James E Crowe5.
Abstract
Hendra (HeV) and Nipah (NiV) viruses are emerging zoonotic pathogens in the Henipavirus genus causing outbreaks of disease with very high case fatality rates. Here, we report the first naturally occurring human monoclonal antibodies (mAbs) against HeV receptor binding protein (RBP). All isolated mAbs neutralized HeV, and some also neutralized NiV. Epitope binning experiments identified five major antigenic sites on HeV-RBP. Animal studies demonstrated that the most potent cross-reactive neutralizing mAbs, HENV-26 and HENV-32, protected ferrets in lethal models of infection with NiV Bangladesh 3 days after exposure. We solved the crystal structures of mAb HENV-26 in complex with both HeV-RBP and NiV-RBP and of mAb HENV-32 in complex with HeV-RBP. The studies reveal diverse sites of vulnerability on RBP recognized by potent human mAbs that inhibit virus by multiple mechanisms. These studies identify promising prophylactic antibodies and define protective epitopes that can be used in rational vaccine design.Entities:
Keywords: B lymphocytes; Hendra virus; Henipavirus infections; Nipah virus; antibodies; antigen-antibody reactions; epitopes; molecular structure; monoclonal; pre-exposure prophylaxis; receptor binding protein; therapy; viral
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Year: 2020 PMID: 33306954 PMCID: PMC7771633 DOI: 10.1016/j.cell.2020.11.023
Source DB: PubMed Journal: Cell ISSN: 0092-8674 Impact factor: 41.582