<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>Kabanovaa, Anna</dc:creator>
  <dc:creator>Perez, Laurent</dc:creator>
  <dc:creator>Lilleri, Daniele</dc:creator>
  <dc:creator>Marcandalli, Jessica</dc:creator>
  <dc:creator>Agatic, Gloria</dc:creator>
  <dc:creator>Becattini, Simone</dc:creator>
  <dc:creator>Preite, Silvia</dc:creator>
  <dc:creator>Fuschillo, Dario</dc:creator>
  <dc:creator>Percivalle,Elena</dc:creator>
  <dc:creator>Sallusto, Federica</dc:creator>
  <dc:creator>Gerna, Giuseppe</dc:creator>
  <dc:creator>Corti, Davide</dc:creator>
  <dc:creator>Lanzavecchia, Antonio</dc:creator>
  <dc:date>2014-12-01</dc:date>
  <dc:description xmlns:ns0="xml" ns0:lang="en">The use of neutralizing antibodies to identify the most effective antigen has been proposed as a  strategy to design vaccines capable of eliciting protective B-cell immunity. In this study, we analyzed  the human antibody response to cytomegalovirus (human cytomegalovirus, HCMV) infection and  found that antibodies to glycoprotein (g)B, a surface glycoprotein that has been developed as a  HCMV vaccine, were primarily nonneutralizing. In contrast, most of the antibodies to the complex  formed by gH, gL, protein (p)UL128, pUL130, and pUL131 (the gHgLpUL128L pentamer)  neutralized HCMV infection with high potency. Based on this analysis, we developed a single  polycistronic vector encoding the five pentamer genes separated by “self-cleaving” 2A peptides to  generate a stably transfected CHO cell line constitutively secreting high levels of recombinant  pentamer that displayed the functional antigenic sites targeted by human neutralizing antibodies.  Immunization of mice with the pentamer formulated with different adjuvants elicited HCMV  neutralizing antibody titers that persisted to high levels over time and that were a hundred- to  thousand-fold higher than those found in individuals that recovered from primary HCMV infection.  Sera from mice immunized with the pentamer vaccine neutralized infection of both epithelial cells  and fibroblasts and prevented cell-to-cell spread and viral dissemination from endothelial cells to  leukocytes. Neutralizing monoclonal antibodies from immunized mice showed the same potency as  human antibodies and targeted the same as well as additional sites on the pentamer. These results  illustrate with a relevant example a general and practical approach of analytic vaccinology for the  development of subunit vaccines against complex pathogens.</dc:description>
  <dc:format>application/pdf</dc:format>
  <dc:identifier>https://susi.usi.ch/global/documents/318791</dc:identifier>
  <dc:identifier>https://n2t.net/ark:/12658/srd1318791</dc:identifier>
  <dc:identifier>https://susi.usi.ch/documents/318791/files/Kabanova_PNAS_2014.pdf</dc:identifier>
  <dc:language>eng</dc:language>
  <dc:relation>info:eu-repo/semantics/altIdentifier/doi/10.1073/pnas.1415310111</dc:relation>
  <dc:relation>info:eu-repo/semantics/altIdentifier/ark/12658/srd1318791</dc:relation>
  <dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
  <dc:rights>License undefined</dc:rights>
  <dc:source>Proceedings of the national academy of sciences of the United States of America. - 2014, vol. 111, no. 50, p. 17965-17970</dc:source>
  <dc:subject xmlns:ns1="xml" ns1:lang="en">Vaccine</dc:subject>
  <dc:subject xmlns:ns2="xml" ns2:lang="en">Human cytomegalovirus</dc:subject>
  <dc:subject xmlns:ns3="xml" ns3:lang="en">Analytic vaccinology</dc:subject>
  <dc:subject>info:eu-repo/classification/udc/61</dc:subject>
  <dc:title xmlns:ns4="xml" ns4:lang="en">Antibody-driven design of a human cytomegalovirus gHgLpUL128L subunit vaccine that selectively elicits potent neutralizing antibodies</dc:title>
  <dc:type>http://purl.org/coar/resource_type/c_6501</dc:type>
</oai_dc:dc>
