<oai_dc:dc xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:oai_dc="http://www.openarchives.org/OAI/2.0/oai_dc/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd">
  <dc:creator>Marcandalli, Jessica</dc:creator>
  <dc:creator>Fiala, Brooke</dc:creator>
  <dc:creator>Ols, Sebastian</dc:creator>
  <dc:creator>Perotti, Michela</dc:creator>
  <dc:creator>de van der Schueren, Willem</dc:creator>
  <dc:creator>Snijder, Joost</dc:creator>
  <dc:creator>Hodge, Edgar</dc:creator>
  <dc:creator>Benhaim, Mark</dc:creator>
  <dc:creator>Ravichandran, Rashmi</dc:creator>
  <dc:creator>Carter, Lauren</dc:creator>
  <dc:creator>Sheffler, Will</dc:creator>
  <dc:creator>Brunner, Livia</dc:creator>
  <dc:creator>Lawrenz, Maria</dc:creator>
  <dc:creator>Dubois, Patrice</dc:creator>
  <dc:creator>Lanzavecchia, Antonio</dc:creator>
  <dc:creator>Sallusto, Federica</dc:creator>
  <dc:creator>Lee, Kelly K.</dc:creator>
  <dc:creator>Veesler, David</dc:creator>
  <dc:creator>Correnti, Colin E.</dc:creator>
  <dc:creator>Stewart, Lance J.</dc:creator>
  <dc:creator>Baker, David</dc:creator>
  <dc:creator>Loré, Karin</dc:creator>
  <dc:creator>Perez, Laurent</dc:creator>
  <dc:creator>King, Neil P.</dc:creator>
  <dc:date>2019-03-07</dc:date>
  <dc:description xmlns:ns0="xml" ns0:lang="en">Respiratory syncytial virus (RSV) is a worldwide public health concern for which no vaccine is  available. Elucidation of the prefusion structure of the RSV F glycoprotein and its identification as  the main target of neutralizing antibodies have provided new opportunities for development of an  effective vaccine. Here, we describe the structure-based design of a self-assembling protein  nanoparticle presenting a prefusion-stabilized variant of the F glycoprotein trimer (DS-Cav1) in a  repetitive array on the nanoparticle exterior. The two-component nature of the nanoparticle scaffold  enabled the production of highly ordered, monodisperse immunogens that display DS-Cav1 at  controllable density. In mice and nonhuman primates, the full-valency nanoparticle immunogen  displaying 20 DS-Cav1 trimers induced neutralizing antibody responses ∼10-fold higher than  trimeric DS-Cav1. These results motivate continued development of this promising nanoparticle  RSV vaccine candidate and establish computationally designed two-component nanoparticles as a  robust and customizable platform for structure-based vaccine design.</dc:description>
  <dc:format>application/pdf</dc:format>
  <dc:identifier>https://susi.usi.ch/global/documents/318938</dc:identifier>
  <dc:identifier>https://localhost:5000/ark:/12658/srd1318938</dc:identifier>
  <dc:identifier>https://susi.usi.ch/documents/318938/files/Marcandalli_Cell_2019.pdf</dc:identifier>
  <dc:language>eng</dc:language>
  <dc:relation>info:eu-repo/semantics/altIdentifier/doi/10.1016/j.cell.2019.01.046</dc:relation>
  <dc:relation>info:eu-repo/semantics/altIdentifier/ark/12658/srd1318938</dc:relation>
  <dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
  <dc:rights>CC BY</dc:rights>
  <dc:source>Cell. - 2019, vol. 177, no. 6, p. 1420-1431.e17</dc:source>
  <dc:subject xmlns:ns1="xml" ns1:lang="en">Computational protein design</dc:subject>
  <dc:subject xmlns:ns2="xml" ns2:lang="en">Self-assembly</dc:subject>
  <dc:subject xmlns:ns3="xml" ns3:lang="en">Vaccines</dc:subject>
  <dc:subject xmlns:ns4="xml" ns4:lang="en">Respiratory syncytial virus</dc:subject>
  <dc:subject xmlns:ns5="xml" ns5:lang="en">Nanoparticles</dc:subject>
  <dc:subject xmlns:ns6="xml" ns6:lang="en">Neutralizing antibodies</dc:subject>
  <dc:subject>info:eu-repo/classification/udc/616</dc:subject>
  <dc:title xmlns:ns7="xml" ns7:lang="en">Induction of potent neutralizing antibody responses by a designed protein nanoparticle accine for respiratory syncytial virus</dc:title>
  <dc:type>http://purl.org/coar/resource_type/c_6501</dc:type>
</oai_dc:dc>
