<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>Zimmermann A</dc:creator>
  <dc:creator>Preynat-Seauve O</dc:creator>
  <dc:creator>Tiercy JM</dc:creator>
  <dc:creator>Krause KH</dc:creator>
  <dc:creator>Villard J</dc:creator>
  <dc:date>2012</dc:date>
  <dc:description xmlns:ns0="xml" ns0:lang="en">High expectations surround the area of stem cells therapeutics. However, the cells' source-adult or embryonic-and the cells' origin-patient-derived autologous or healthy donor genetically unrelated-remain subjects of debate. Autologous origins have the advantage of a theoretical absence of immune rejection by the recipient. However, this approach has several limitations with regard to the disease of the recipient and to potential problems with the generation, expansion, and manipulation of autologous induced pluripotent stem cells (iPS cells) preparation. An alternative to using autologous cells is the establishment of a bank of well-characterized adult cells that would be used to generate iPS cells and their derivatives. In the context of transplantation, such cells would come from genetically unrelated donors and the immune system of the recipient would reject the graft without immunosuppressive therapy. To minimize the risk of rejection, human leukocyte antigen (HLA) compatibility is certainly the best option, and the establishment of an HLA-organized bank would mean having a limited number of stem cells that would be sufficient for a large number of recipients. The concept of haplobanking with HLA homozygous cell lines would also limit the number of HLA mismatches, but such an approach will not necessarily be less immunogenic in terms of selection criteria, because of the limited number of HLA-compatible loci and the level of HLA typing resolution.</dc:description>
  <dc:format>application/pdf</dc:format>
  <dc:identifier>https://sonar.ch/global/documents/88044</dc:identifier>
  <dc:language>eng</dc:language>
  <dc:relation>info:eu-repo/semantics/altIdentifier/doi/10.1089/scd.2012.0088</dc:relation>
  <dc:relation>info:eu-repo/semantics/altIdentifier/pmid/22559254</dc:relation>
  <dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
  <dc:source>Stem cells and development. - 2012</dc:source>
  <dc:subject xmlns:ns1="xml" ns1:lang="en">Cell Culture Techniques</dc:subject>
  <dc:subject xmlns:ns2="xml" ns2:lang="en">Embryo, Mammalian</dc:subject>
  <dc:subject xmlns:ns3="xml" ns3:lang="en">Graft Rejection</dc:subject>
  <dc:subject xmlns:ns4="xml" ns4:lang="en">HLA Antigens</dc:subject>
  <dc:subject xmlns:ns5="xml" ns5:lang="en">Haplotypes</dc:subject>
  <dc:subject xmlns:ns6="xml" ns6:lang="en">Histocompatibility Testing</dc:subject>
  <dc:subject xmlns:ns7="xml" ns7:lang="en">Homozygote</dc:subject>
  <dc:subject xmlns:ns8="xml" ns8:lang="en">Humans</dc:subject>
  <dc:subject xmlns:ns9="xml" ns9:lang="en">Induced Pluripotent Stem Cells</dc:subject>
  <dc:subject xmlns:ns10="xml" ns10:lang="en">Parthenogenesis</dc:subject>
  <dc:subject xmlns:ns11="xml" ns11:lang="en">Stem Cell Research</dc:subject>
  <dc:subject xmlns:ns12="xml" ns12:lang="en">Tissue Banks</dc:subject>
  <dc:subject xmlns:ns13="xml" ns13:lang="en">Tissue Donors</dc:subject>
  <dc:title xmlns:ns14="xml" ns14:lang="en">Haplotype-based banking of human pluripotent stem cells for transplantation: potential and limitations.</dc:title>
  <dc:type>http://purl.org/coar/resource_type/c_6501</dc:type>
</oai_dc:dc>