Source:http://linkedlifedata.com/resource/pubmed/id/18976293
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
1
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pubmed:dateCreated |
2009-1-12
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pubmed:abstractText |
Antigen-specific T cells, which express CD154 rapidly, but remain untested in alloimmunity, were measured with flow cytometry in 16-h MLR of 58 identically-immunosuppressed children with liver transplantation (LTx), to identify Rejectors (who had experienced biopsy-proven rejection within 60 days posttransplantation). Thirty-one children were sampled once, cross-sectionally. Twenty-seven children were sampled longitudinally, pre-LTx, and at 1-60 and 61-200 days after LTx. Results were correlated with proliferative alloresponses measured by CFSE-dye dilution (n = 23), and CTLA4, a negative T-cell costimulator, which antagonizes CD154-mediated effects (n = 31). In cross-sectional observations, logistic regression and leave-one-out cross-validation identified donor-specific, CD154 + T-cytotoxic (Tc)-memory cells as best associated with rejection outcomes. In the longitudinal cohort, (1) the association between CD154 + Tc-memory cells and rejection outcomes was replicated with sensitivity/specificity 92.3%/84.6% for observations at 1-60 days, and (2) elevated pre-LTx CD154 + Tc-memory cell responses were associated with significantly increased incidence (p = 0.02) and hazard (HR = 7.355) of rejection in survival/proportional hazard analysis. CD154 expression correlated with proliferative alloresponses (r = 0.835, p = 7.1e-07), and inversely with CTLA4 expression of allospecific CD154 + Tc-memory cells (r =-0.706, p = 3.0e-05). Allospecific CD154 + T-helper-memory cells, not CD154 + Tc-memory, were inhibited by increasing Tacrolimus concentrations (p = 0.026). Collectively, allospecific CD154 + T cells provide an estimate of rejection risk in children with LTx.
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pubmed:grant | |
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 |
Jan
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pubmed:issn |
1600-6143
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pubmed:author |
pubmed-author:AshokkumarCC,
pubmed-author:BondGG,
pubmed-author:DemetrisAA,
pubmed-author:DobbersteinJJ,
pubmed-author:HiggsB WBW,
pubmed-author:JaffeRR,
pubmed-author:JanoskyJJ,
pubmed-author:MazariegosGG,
pubmed-author:SindhiRR,
pubmed-author:SoltysKK,
pubmed-author:SurMM,
pubmed-author:TalukdarAA,
pubmed-author:ThomsonA WAW,
pubmed-author:WilsonPP,
pubmed-author:ZeeviAA
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pubmed:issnType |
Electronic
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pubmed:volume |
9
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
179-91
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pubmed:dateRevised |
2011-11-17
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pubmed:meshHeading |
pubmed-meshheading:18976293-Antigens, CD,
pubmed-meshheading:18976293-CD40 Ligand,
pubmed-meshheading:18976293-CTLA-4 Antigen,
pubmed-meshheading:18976293-Child,
pubmed-meshheading:18976293-Child, Preschool,
pubmed-meshheading:18976293-Cohort Studies,
pubmed-meshheading:18976293-Female,
pubmed-meshheading:18976293-Graft Rejection,
pubmed-meshheading:18976293-Humans,
pubmed-meshheading:18976293-Immunologic Memory,
pubmed-meshheading:18976293-Liver Transplantation,
pubmed-meshheading:18976293-Male,
pubmed-meshheading:18976293-T-Lymphocytes
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pubmed:year |
2009
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pubmed:articleTitle |
Allospecific CD154+ T cells associate with rejection risk after pediatric liver transplantation.
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pubmed:affiliation |
University of Pittsburgh and Children's Hospital of Pittsburgh, Department of Transplant Surgery, Pittsburgh, PA, USA.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't,
Research Support, N.I.H., Extramural
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