| Literature DB >> 31100268 |
Sandhya Bangaru1, Shanshan Lang2, Michael Schotsaert3, Hillary A Vanderven4, Xueyong Zhu2, Nurgun Kose5, Robin Bombardi5, Jessica A Finn1, Stephen J Kent4, Pavlo Gilchuk5, Iuliia Gilchuk5, Hannah L Turner2, Adolfo García-Sastre6, Sheng Li7, Andrew B Ward2, Ian A Wilson8, James E Crowe9.
Abstract
Here, we describe the discovery of a naturally occurring human antibody (Ab), FluA-20, that recognizes a new site of vulnerability on the hemagglutinin (HA) head domain and reacts with most influenza A viruses. Structural characterization of FluA-20 with H1 and H3 head domains revealed a novel epitope in the HA trimer interface, suggesting previously unrecognized dynamic features of the trimeric HA protein. The critical HA residues recognized by FluA-20 remain conserved across most subtypes of influenza A viruses, which explains the Ab's extraordinary breadth. The Ab rapidly disrupted the integrity of HA protein trimers, inhibited cell-to-cell spread of virus in culture, and protected mice against challenge with viruses of H1N1, H3N2, H5N1, or H7N9 subtypes when used as prophylaxis or therapy. The FluA-20 Ab has uncovered an exceedingly conserved protective determinant in the influenza HA head domain trimer interface that is an unexpected new target for anti-influenza therapeutics and vaccines.Entities:
Keywords: B-lymphocytes; antibodies; antibody-dependent cell cytotoxicity; antigen-antibody reactions; hemagglutinin glycoproteins; influenza A virus; influenza virus; monoclonal; viral
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Year: 2019 PMID: 31100268 PMCID: PMC6629437 DOI: 10.1016/j.cell.2019.04.011
Source DB: PubMed Journal: Cell ISSN: 0092-8674 Impact factor: 41.582