pubmed-article:16951047 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:16951047 | lifeskim:mentions | umls-concept:C0007634 | lld:lifeskim |
pubmed-article:16951047 | lifeskim:mentions | umls-concept:C1332717 | lld:lifeskim |
pubmed-article:16951047 | lifeskim:mentions | umls-concept:C1706438 | lld:lifeskim |
pubmed-article:16951047 | lifeskim:mentions | umls-concept:C0018787 | lld:lifeskim |
pubmed-article:16951047 | lifeskim:mentions | umls-concept:C0450127 | lld:lifeskim |
pubmed-article:16951047 | lifeskim:mentions | umls-concept:C0085358 | lld:lifeskim |
pubmed-article:16951047 | lifeskim:mentions | umls-concept:C0070410 | lld:lifeskim |
pubmed-article:16951047 | lifeskim:mentions | umls-concept:C0038952 | lld:lifeskim |
pubmed-article:16951047 | lifeskim:mentions | umls-concept:C1512840 | lld:lifeskim |
pubmed-article:16951047 | lifeskim:mentions | umls-concept:C1413244 | lld:lifeskim |
pubmed-article:16951047 | lifeskim:mentions | umls-concept:C2698600 | lld:lifeskim |
pubmed-article:16951047 | lifeskim:mentions | umls-concept:C0392756 | lld:lifeskim |
pubmed-article:16951047 | lifeskim:mentions | umls-concept:C0033268 | lld:lifeskim |
pubmed-article:16951047 | lifeskim:mentions | umls-concept:C1879547 | lld:lifeskim |
pubmed-article:16951047 | lifeskim:mentions | umls-concept:C1515895 | lld:lifeskim |
pubmed-article:16951047 | lifeskim:mentions | umls-concept:C0205228 | lld:lifeskim |
pubmed-article:16951047 | pubmed:issue | 1 | lld:pubmed |
pubmed-article:16951047 | pubmed:dateCreated | 2007-1-10 | lld:pubmed |
pubmed-article:16951047 | pubmed:abstractText | Perforin is a cytolytic mediator produced by cytotoxic T cells (CD8(+) cells) and natural killer cells. We previously reported that ex vivo IL-10 gene therapy induced apoptosis of allogenic infiltrative CD8(+) cells and significantly prolonged cardiac allograft survival. To further test the hypothesis that localized IL-10 overexpression in cardiac allografts may also effect the alloreactive CD8(+) T cell function by downregulating its perforin production, we used a rabbit functional heterotopic allograft heart transplant model. Human recombinant IL-10 gene complexed with liposome was intracoronary delivered into the cardiac allografts ex vivo. The percentage of apoptotic infiltrative CD8(+) cells in cardiac allografts was increased 6-fold in the gene therapy group vs. the control group, whereas the percentage of perforin-positive CD8(+) cells was decreased 2.9-fold (P < 0.01). Perforin expression level in the allograft myocardium of the gene therapy group was deceased 3.2-fold (P < 0.01). The amount of infiltrative perforin-positive CD8(+) cells and perforin expression level were inversely correlated with IL-10 transgene and protein expression level in the myocardium of cardiac allografts (P < 0.01), the percentage of apoptotic cardiac myocytes (P < 0.01), and the peak left ventricular systolic pressure of cardiac allografts (P < 0.01) but significantly correlated with the infiltrative T cell cytotoxicity (P < 0.01) and allograft rejection score (P < 0.01). These results suggest that localized IL-10 gene therapy prolongs cardiac allograft survival, at least in part, through downregulation of perforin production by activated allogenic CD8(+) T cells. Reduction of cytolytic function of cytotoxic effector cells prevents the apoptosis of cardiac myocytes. | lld:pubmed |
pubmed-article:16951047 | pubmed:language | eng | lld:pubmed |
pubmed-article:16951047 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:16951047 | pubmed:citationSubset | IM | lld:pubmed |
pubmed-article:16951047 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:16951047 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:16951047 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:16951047 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:16951047 | pubmed:status | MEDLINE | lld:pubmed |
pubmed-article:16951047 | pubmed:month | Jan | lld:pubmed |
pubmed-article:16951047 | pubmed:issn | 0363-6135 | lld:pubmed |
pubmed-article:16951047 | pubmed:author | pubmed-author:LaksHillelH | lld:pubmed |
pubmed-article:16951047 | pubmed:author | pubmed-author:MOONM WMW | lld:pubmed |
pubmed-article:16951047 | pubmed:author | pubmed-author:OshimaKiyohir... | lld:pubmed |
pubmed-article:16951047 | pubmed:author | pubmed-author:CuiGuanggenG | lld:pubmed |
pubmed-article:16951047 | pubmed:author | pubmed-author:TungThomasT | lld:pubmed |
pubmed-article:16951047 | pubmed:author | pubmed-author:OkotieOnisuru... | lld:pubmed |
pubmed-article:16951047 | pubmed:issnType | Print | lld:pubmed |
pubmed-article:16951047 | pubmed:volume | 292 | lld:pubmed |
pubmed-article:16951047 | pubmed:owner | NLM | lld:pubmed |
pubmed-article:16951047 | pubmed:authorsComplete | Y | lld:pubmed |
pubmed-article:16951047 | pubmed:pagination | H277-84 | lld:pubmed |
pubmed-article:16951047 | pubmed:dateRevised | 2007-11-15 | lld:pubmed |
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pubmed-article:16951047 | pubmed:year | 2007 | lld:pubmed |
pubmed-article:16951047 | pubmed:articleTitle | Exogenous IL-10 overexpression reduces perforin production by activated allogenic CD8+ cells and prolongs cardiac allograft survival. | lld:pubmed |
pubmed-article:16951047 | pubmed:affiliation | Division of Cardiothoracic Surgery, Dept. of Surgery, UCLA Medical Center, David Geffen School of Medicine in UCLA, 10833 Le Conte Ave., 47-123 CHS, Los Angeles, CA 90095-1679, USA. | lld:pubmed |
pubmed-article:16951047 | pubmed:publicationType | Journal Article | lld:pubmed |