<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>Curcio-Vonlanthen V</dc:creator>
  <dc:creator>Schneider CH</dc:creator>
  <dc:creator>Frutig K</dc:creator>
  <dc:creator>Blaser K</dc:creator>
  <dc:creator>Kalbacher H</dc:creator>
  <dc:date>1997</dc:date>
  <dc:description xmlns:ns0="xml" ns0:lang="en">Based on immunogenicity studies, two T-cell epitopes in melittin were found to be functional in guinea pigs, one being centrally located, the other one residing in the C-terminal chain. In Balb/c mice only the central epitope was found to be active. A human T-cell clone was found by T-cell proliferation studies to employ strictly the C-terminal chain. Truncation of melittin peptides at the N-terminus did not markedly affect the capacity of guinea pigs to develop anti-IgG responses towards peptidic epitopes and towards a C-terminally attached haptenic group. Attachment of various substituents inside and outside the T-cell epitopic areas had no marked effect on antibody responses. In contrast, the substituents positioned within a T-cell epitope abolished T-cell proliferation. This difference between whole animal data and cellular in vitro responses is presently not understood.</dc:description>
  <dc:identifier>https://sonar.ch/global/documents/32764</dc:identifier>
  <dc:language>eng</dc:language>
  <dc:relation>info:eu-repo/semantics/altIdentifier/doi/10.1002/(sici)1099-1387(199707)3:4&lt;267::aid-psc106&gt;3.0.co;2-7</dc:relation>
  <dc:relation>info:eu-repo/semantics/altIdentifier/pmid/9262645</dc:relation>
  <dc:source>Journal of peptide science : an official publication of the European Peptide Society. - 1997</dc:source>
  <dc:subject xmlns:ns1="xml" ns1:lang="en">Amino Acid Sequence</dc:subject>
  <dc:subject xmlns:ns2="xml" ns2:lang="en">Animals</dc:subject>
  <dc:subject xmlns:ns3="xml" ns3:lang="en">Cell Division</dc:subject>
  <dc:subject xmlns:ns4="xml" ns4:lang="en">Cell Line</dc:subject>
  <dc:subject xmlns:ns5="xml" ns5:lang="en">Clone Cells</dc:subject>
  <dc:subject xmlns:ns6="xml" ns6:lang="en">Epitopes, T-Lymphocyte</dc:subject>
  <dc:subject xmlns:ns7="xml" ns7:lang="en">Guinea Pigs</dc:subject>
  <dc:subject xmlns:ns8="xml" ns8:lang="en">Humans</dc:subject>
  <dc:subject xmlns:ns9="xml" ns9:lang="en">Melitten</dc:subject>
  <dc:subject xmlns:ns10="xml" ns10:lang="en">Mice</dc:subject>
  <dc:subject xmlns:ns11="xml" ns11:lang="en">Mice, Inbred BALB C</dc:subject>
  <dc:subject xmlns:ns12="xml" ns12:lang="en">Molecular Sequence Data</dc:subject>
  <dc:subject xmlns:ns13="xml" ns13:lang="en">T-Lymphocytes</dc:subject>
  <dc:title xmlns:ns14="xml" ns14:lang="en">Molecular parameters in melittin immunogenicity.</dc:title>
  <dc:type>http://purl.org/coar/resource_type/c_6501</dc:type>
</oai_dc:dc>
