| Literature DB >> 26806128 |
Andrew I Flyak1, Xiaoli Shen2, Charles D Murin3, Hannah L Turner4, Joshua A David4, Marnie L Fusco5, Rebecca Lampley6, Nurgun Kose6, Philipp A Ilinykh2, Natalia Kuzmina2, Andre Branchizio6, Hannah King6, Leland Brown6, Christopher Bryan7, Edgar Davidson7, Benjamin J Doranz7, James C Slaughter8, Gopal Sapparapu6, Curtis Klages9, Thomas G Ksiazek10, Erica Ollmann Saphire11, Andrew B Ward4, Alexander Bukreyev12, James E Crowe13.
Abstract
Recent studies have suggested that antibody-mediated protection against the Ebolaviruses may be achievable, but little is known about whether or not antibodies can confer cross-reactive protection against viruses belonging to diverse Ebolavirus species, such as Ebola virus (EBOV), Sudan virus (SUDV), and Bundibugyo virus (BDBV). We isolated a large panel of human monoclonal antibodies (mAbs) against BDBV glycoprotein (GP) using peripheral blood B cells from survivors of the 2007 BDBV outbreak in Uganda. We determined that a large proportion of mAbs with potent neutralizing activity against BDBV bind to the glycan cap and recognize diverse epitopes within this major antigenic site. We identified several glycan cap-specific mAbs that neutralized multiple ebolaviruses, including SUDV, and a cross-reactive mAb that completely protected guinea pigs from the lethal challenge with heterologous EBOV. Our results provide a roadmap to develop a single antibody-based treatment effective against multiple Ebolavirus infections.Entities:
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Year: 2016 PMID: 26806128 PMCID: PMC4733404 DOI: 10.1016/j.cell.2015.12.022
Source DB: PubMed Journal: Cell ISSN: 0092-8674 Impact factor: 41.582