| Literature DB >> 32620559 |
Matthew R Vogt1, Jianing Fu2, Nurgun Kose3, Lauren E Williamson4, Robin Bombardi3, Ian Setliff5, Ivelin S Georgiev3,4, Thomas Klose2, Michael G Rossmann2, Yury A Bochkov6, James E Gern6,7, Richard J Kuhn2, James E Crowe8,3,4,5.
Abstract
Enterovirus D68 (EV-D68) causes outbreaks of respiratory illness, and there is increasing evidence that it causes outbreaks of acute flaccid myelitis (AFM). There are no licensed therapies to prevent or treat EV-D68 infection or AFM disease. We isolated a panel of EV-D68-reactive human monoclonal antibodies that recognize diverse antigenic variants from participants with prior infection. One potently neutralizing cross-reactive antibody, EV68-228, protected mice from respiratory and neurologic disease when given either before or after infection. Cryo-electron microscopy studies revealed that EV68-228 and another potently neutralizing antibody (EV68-159) bound around the fivefold or threefold axes of symmetry on virion particles, respectively. The structures suggest diverse mechanisms of action by these antibodies. The high potency and effectiveness observed in vivo suggest that antibodies are a mechanistic correlate of protection against AFM disease and are candidates for clinical use in humans with EV-D68 infection.Entities:
Mesh:
Substances:
Year: 2020 PMID: 32620559 PMCID: PMC7418079 DOI: 10.1126/sciimmunol.aba4902
Source DB: PubMed Journal: Sci Immunol ISSN: 2470-9468