Source:http://linkedlifedata.com/resource/pubmed/id/17496539
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
9
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pubmed:dateCreated |
2007-5-14
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pubmed:abstractText |
CD154-specific antibodies have been shown to prevent acute rejection in many preclinical models including nonhuman primates (NHPs). However, they have been ineffective in pilot clinical trials, suggesting a need for more robust preclinical analysis. One factor affecting the disparate results may be related to the recipient's immune activation state. Specifically, adult humans have a high percentage of memory-phenotype T cells compared to young animals. Postdepletional homeostatic repopulation has been shown to enrich for memory-phenotype T cells and interfere with CD154-based therapies in rodents.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
May
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pubmed:issn |
0041-1337
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:day |
15
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pubmed:volume |
83
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
1219-25
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pubmed:meshHeading |
pubmed-meshheading:17496539-Animals,
pubmed-meshheading:17496539-Blood Transfusion,
pubmed-meshheading:17496539-CD40 Ligand,
pubmed-meshheading:17496539-Graft Rejection,
pubmed-meshheading:17496539-Homeostasis,
pubmed-meshheading:17496539-Immunologic Memory,
pubmed-meshheading:17496539-Immunosuppressive Agents,
pubmed-meshheading:17496539-Kidney Transplantation,
pubmed-meshheading:17496539-Lymphocyte Activation,
pubmed-meshheading:17496539-Macaca fascicularis,
pubmed-meshheading:17496539-Phenotype,
pubmed-meshheading:17496539-Sirolimus,
pubmed-meshheading:17496539-T-Lymphocytes,
pubmed-meshheading:17496539-Thymectomy,
pubmed-meshheading:17496539-Tissue Donors,
pubmed-meshheading:17496539-Transplantation, Homologous
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pubmed:year |
2007
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pubmed:articleTitle |
CD154 blockade, sirolimus, and donor-specific transfusion prevents renal allograft rejection in cynomolgus monkeys despite homeostatic T-cell activation.
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pubmed:affiliation |
Transplantation Branch, National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, Department of Health and Human Services, Bethesda, MD, USA.
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pubmed:publicationType |
Journal Article,
Research Support, N.I.H., Intramural
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