<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>Speiser DE</dc:creator>
  <dc:creator>Liénard D</dc:creator>
  <dc:creator>Rufer N</dc:creator>
  <dc:creator>Rubio-Godoy V</dc:creator>
  <dc:creator>Rimoldi D</dc:creator>
  <dc:creator>Lejeune F</dc:creator>
  <dc:creator>Krieg AM</dc:creator>
  <dc:creator>Cerottini JC</dc:creator>
  <dc:creator>Romero P</dc:creator>
  <dc:date>2005</dc:date>
  <dc:description xmlns:ns0="xml" ns0:lang="en">The induction of potent CD8+ T cell responses by vaccines to fight microbes or tumors remains a major challenge, as many candidates for human vaccines have proved to be poorly immunogenic. Deoxycytidyl-deoxyguanosin oligodeoxynucleotides (CpG ODNs) trigger Toll-like receptor 9, resulting in dendritic cell maturation that can enhance immunogenicity of peptide-based vaccines in mice. We tested whether a synthetic ODN, CpG 7909, could improve human tumor antigen-specific CD8+ T cell responses. Eight HLA-A2+ melanoma patients received 4 monthly vaccinations of low-dose CpG 7909 mixed with melanoma antigen A (Melan-A; identical to MART-1) analog peptide and incomplete Freund's adjuvant. All patients exhibited rapid and strong antigen-specific T cell responses: the frequency of Melan-A-specific T cells reached over 3% of circulating CD8+ T cells. This was one order of magnitude higher than the frequency seen in 8 control patients treated similarly but without CpG and 1-3 orders of magnitude higher than that seen in previous studies with synthetic vaccines. The enhanced T cell populations consisted primarily of effector memory cells, which in part secreted IFN- and expressed granzyme B and perforin ex vivo. In vitro, T cell clones recognized and killed melanoma cells in an antigen-specific manner. Thus, CpG 7909 is an efficient vaccine adjuvant that promotes strong antigen-specific CD8+ T cell responses in humans.</dc:description>
  <dc:format>application/pdf</dc:format>
  <dc:identifier>https://sonar.ch/global/documents/139277</dc:identifier>
  <dc:language>eng</dc:language>
  <dc:relation>info:eu-repo/semantics/altIdentifier/doi/10.1172/JCI23373</dc:relation>
  <dc:relation>info:eu-repo/semantics/altIdentifier/pmid/15696196</dc:relation>
  <dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
  <dc:source>The Journal of clinical investigation. - 2005</dc:source>
  <dc:subject xmlns:ns1="xml" ns1:lang="en">Animals</dc:subject>
  <dc:subject xmlns:ns2="xml" ns2:lang="en">Antigens, Neoplasm</dc:subject>
  <dc:subject xmlns:ns3="xml" ns3:lang="en">CD8-Positive T-Lymphocytes</dc:subject>
  <dc:subject xmlns:ns4="xml" ns4:lang="en">Cancer Vaccines</dc:subject>
  <dc:subject xmlns:ns5="xml" ns5:lang="en">Freund's Adjuvant</dc:subject>
  <dc:subject xmlns:ns6="xml" ns6:lang="en">HLA-A2 Antigen</dc:subject>
  <dc:subject xmlns:ns7="xml" ns7:lang="en">Humans</dc:subject>
  <dc:subject xmlns:ns8="xml" ns8:lang="en">Interferon-gamma</dc:subject>
  <dc:subject xmlns:ns9="xml" ns9:lang="en">Lipids</dc:subject>
  <dc:subject xmlns:ns10="xml" ns10:lang="en">Lymphocyte Activation</dc:subject>
  <dc:subject xmlns:ns11="xml" ns11:lang="en">MART-1 Antigen</dc:subject>
  <dc:subject xmlns:ns12="xml" ns12:lang="en">Melanoma</dc:subject>
  <dc:subject xmlns:ns13="xml" ns13:lang="en">Neoplasm Proteins</dc:subject>
  <dc:subject xmlns:ns14="xml" ns14:lang="en">Oligodeoxyribonucleotides</dc:subject>
  <dc:subject xmlns:ns15="xml" ns15:lang="en">Quality Control</dc:subject>
  <dc:subject xmlns:ns16="xml" ns16:lang="en">Vaccination</dc:subject>
  <dc:title xmlns:ns17="xml" ns17:lang="en">Rapid and strong human CD8+ T cell responses to vaccination with peptide, IFA, and CpG oligodeoxynucleotide 7909.</dc:title>
  <dc:type>http://purl.org/coar/resource_type/c_6501</dc:type>
</oai_dc:dc>
