<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>De Benedictis, Paola</dc:creator>
  <dc:creator>Minola, Andrea</dc:creator>
  <dc:creator>Rota Nodari, Elena</dc:creator>
  <dc:creator>Aiello, Roberta</dc:creator>
  <dc:creator>Zecchin, Barbara</dc:creator>
  <dc:creator>Salomoni, Angela</dc:creator>
  <dc:creator>Foglierini, Mathilde</dc:creator>
  <dc:creator>Agatic, Gloria</dc:creator>
  <dc:creator>Vanzetta, Fabrizia</dc:creator>
  <dc:creator>Lavenir, Rachel</dc:creator>
  <dc:creator>Lepelletier, Anthony</dc:creator>
  <dc:creator>Bentley, Emma</dc:creator>
  <dc:creator>Weiss, Robin</dc:creator>
  <dc:creator>Cattoli, Giovanni</dc:creator>
  <dc:creator>Capua, Ilaria</dc:creator>
  <dc:creator>Sallusto, Federica</dc:creator>
  <dc:creator>Wright, Edward</dc:creator>
  <dc:creator>Lanzavecchia, Antonio</dc:creator>
  <dc:creator>Bourhy, Hervé</dc:creator>
  <dc:creator>Corti, Davide</dc:creator>
  <dc:date>2016-03-18</dc:date>
  <dc:description xmlns:ns0="xml" ns0:lang="en">Currently available rabies post‐exposure prophylaxis (PEP) for use in humans includes equine  or human rabies immunoglobulins (RIG). The replacement of RIG with an equally or more  potent and safer product is strongly encouraged due to the high costs and limited availability  of existing RIG. In this study, we identified two broadly neutralizing human monoclonal  antibodies that represent a valid and affordable alternative to RIG in rabies PEP. Memory B  cells from four selected vaccinated donors were immortalized and monoclonal antibodies  were tested for neutralizing activity and epitope specificity. Two antibodies, identified as  RVC20 and RVC58 (binding to antigenic site I and III, respectively), were selected for their  potency and broad‐spectrum reactivity. In vitro, RVC20 and RVC58 were able to neutralize all  35 rabies virus (RABV) and 25 non‐RABV lyssaviruses. They showed higher potency and  breath compared to antibodies under clinical development (namely CR57, CR4098, and  RAB1) and commercially available human RIG. In vivo, the RVC20–RVC58 cocktail protected  Syrian hamsters from a lethal RABV challenge and did not affect the endogenous hamster  post‐vaccination antibody response.</dc:description>
  <dc:format>application/pdf</dc:format>
  <dc:identifier>https://susi.usi.ch/global/documents/319138</dc:identifier>
  <dc:identifier>https://localhost:5000/ark:/12658/srd1319138</dc:identifier>
  <dc:identifier>https://susi.usi.ch/documents/319138/files/DeBenedictis_EMM_2016.pdf</dc:identifier>
  <dc:language>eng</dc:language>
  <dc:relation>info:eu-repo/semantics/altIdentifier/doi/10.15252/emmm.201505986</dc:relation>
  <dc:relation>info:eu-repo/semantics/altIdentifier/ark/12658/srd1319138</dc:relation>
  <dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
  <dc:rights>CC BY</dc:rights>
  <dc:source>EMBO molecular medicine. - 2016, vol. 8, no. 4, p. 407-421</dc:source>
  <dc:subject xmlns:ns1="xml" ns1:lang="en">Human monoclonal antibody</dc:subject>
  <dc:subject xmlns:ns2="xml" ns2:lang="en">Lyssaviruses</dc:subject>
  <dc:subject xmlns:ns3="xml" ns3:lang="en">Post-exposure prophylaxis</dc:subject>
  <dc:subject xmlns:ns4="xml" ns4:lang="en">Rabies</dc:subject>
  <dc:subject>info:eu-repo/classification/udc/61</dc:subject>
  <dc:title xmlns:ns5="xml" ns5:lang="en">Development of broad‐spectrum human monoclonal antibodies for rabies post‐exposure prophylaxis</dc:title>
  <dc:type>http://purl.org/coar/resource_type/c_6501</dc:type>
</oai_dc:dc>
