<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>Lilienfeld BG</dc:creator>
  <dc:creator>Crew MD</dc:creator>
  <dc:creator>Forte P</dc:creator>
  <dc:creator>Baumann BC</dc:creator>
  <dc:creator>Seebach JD</dc:creator>
  <dc:date>2007</dc:date>
  <dc:description xmlns:ns0="xml" ns0:lang="en">BACKGROUND
The susceptibility of porcine endothelial cells (pEC) to human natural killer (NK) cells is related to the failure of human major histocompatibility complex (MHC)-specific killer inhibitory receptors to recognize porcine MHC class I molecules. The aims of this study were (i) to assess the protection of pEC against xenogeneic NK-mediated cytotoxicity afforded by the stable expression of HLA-E single chain trimers (SCT) composed of a canonical HLA-E binding peptide antigen, VMAPRTLIL, the mature human beta2-microglobulin, and the mature HLA-E heavy chain, and (ii) to test whether HLA-E expression on pEC and porcine lymphoblastoid cells affects the adhesion of human NK cells.


METHODS
Porcine EC lines expressing different levels of HLA-E SCT were generated by Ca(2)PO(4)-transfection followed by limiting dilution cloning. Surface expression of HLA-E was measured by flow cytometry. Susceptibility of transfected pEC lines against human NK cells was tested in (51)Cr-release cytotoxicity assays. Interactions between human NK cells and HLA-E positive pEC or porcine lymphoblastoid cells were further addressed in adhesion and conjugation assays.


RESULTS
The level of protection of pEC from human NK-mediated cytotoxicity correlated with the intensity of surface HLA-E expression. Furthermore, the HLA-E SCT-mediated protection was specifically reversed by blocking the HLA-E specific NK inhibitory receptor CD94/NKG2A. HLA-E expression does neither affect the adhesion of human NK cells to pEC nor the heteroconjugate formation between human NK and porcine 13271.10 cells.


CONCLUSIONS
Stable surface expression of HLA-E on pEC was achieved in the absence of extrinsic peptide pulsing and provided partial protection from human NK cytotoxicity. Though insufficient to inhibit xenogeneic NK cell reactivity completely, transgenic HLA-E expression on pig organs might contribute to a successful application of clinical xenotransplantation in combination with other protective strategies.</dc:description>
  <dc:identifier>https://sonar.ch/global/documents/4240</dc:identifier>
  <dc:language>eng</dc:language>
  <dc:relation>info:eu-repo/semantics/altIdentifier/doi/10.1111/j.1399-3089.2007.00378.x</dc:relation>
  <dc:relation>info:eu-repo/semantics/altIdentifier/pmid/17381687</dc:relation>
  <dc:source>Xenotransplantation. - 2007</dc:source>
  <dc:subject xmlns:ns1="xml" ns1:lang="en">Animals</dc:subject>
  <dc:subject xmlns:ns2="xml" ns2:lang="en">Antibodies, Heterophile</dc:subject>
  <dc:subject xmlns:ns3="xml" ns3:lang="en">Cell Adhesion</dc:subject>
  <dc:subject xmlns:ns4="xml" ns4:lang="en">Cell Communication</dc:subject>
  <dc:subject xmlns:ns5="xml" ns5:lang="en">Cell Line</dc:subject>
  <dc:subject xmlns:ns6="xml" ns6:lang="en">Cytotoxicity, Immunologic</dc:subject>
  <dc:subject xmlns:ns7="xml" ns7:lang="en">Endothelium, Vascular</dc:subject>
  <dc:subject xmlns:ns8="xml" ns8:lang="en">Gene Expression Regulation</dc:subject>
  <dc:subject xmlns:ns9="xml" ns9:lang="en">HLA Antigens</dc:subject>
  <dc:subject xmlns:ns10="xml" ns10:lang="en">Histocompatibility Antigens Class I</dc:subject>
  <dc:subject xmlns:ns11="xml" ns11:lang="en">Humans</dc:subject>
  <dc:subject xmlns:ns12="xml" ns12:lang="en">Killer Cells, Natural</dc:subject>
  <dc:subject xmlns:ns13="xml" ns13:lang="en">NK Cell Lectin-Like Receptor Subfamily D</dc:subject>
  <dc:subject xmlns:ns14="xml" ns14:lang="en">Swine</dc:subject>
  <dc:subject xmlns:ns15="xml" ns15:lang="en">Transfection</dc:subject>
  <dc:subject xmlns:ns16="xml" ns16:lang="en">Transgenes</dc:subject>
  <dc:subject xmlns:ns17="xml" ns17:lang="en">Transplantation, Heterologous</dc:subject>
  <dc:title xmlns:ns18="xml" ns18:lang="en">Transgenic expression of HLA-E single chain trimer protects porcine endothelial cells against human natural killer cell-mediated cytotoxicity.</dc:title>
  <dc:type>http://purl.org/coar/resource_type/c_6501</dc:type>
</oai_dc:dc>
