Matches in SemOpenAlex for { <https://semopenalex.org/work/W2326365518> ?p ?o ?g. }
- W2326365518 endingPage "140" @default.
- W2326365518 startingPage "131" @default.
- W2326365518 abstract "In Brief Background Allospecific CD154+T-cytotoxic memory cells (CD154+TcM) predict acute cellular rejection after liver transplantation (LTx) or intestine transplantation (ITx) in small cohorts of children and can enhance immunosuppression management, but await validation and clinical implementation. Methods To establish safety and probable benefit, CD154+TcM were measured in cryopreserved samples from 214 children younger than 21 years (National Clinical Trial 1163578). Training set samples (n = 158) were tested with research-grade reagents and 122 independent validation set samples were tested with current good manufacturing practices-manufactured reagents after assay standardization and reproducibility testing. Recipient CD154+TcM induced by stimulation with donor cells were expressed as a fraction of those induced by HLA nonidentical cells in parallel cultures. The resulting immunoreactivity index (IR) if greater than 1 implies increased rejection-risk. Results Training and validation set subjects were demographically similar. Mean coefficient of test variation was less than 10% under several conditions. Logistic regression incorporating several confounding variables identified separate pretransplant and posttransplant IR thresholds for prediction of rejection in the respective training set samples. An IR of 1.1 or greater in posttransplant training samples and IR of 1.23 or greater in pretransplant training samples predicted LTx or ITx rejection in corresponding validation set samples in the 60-day postsampling period with sensitivity, specificity, positive, and negative predictive values of 84%, 80%, 64%, and 92%, respectively (area under the receiver operator characteristic curve, 0.792), and 57%, 89%, 78%, and 74%, respectively (area under the receiver operator characteristic curve, 0.848). No adverse events were encountered due to phlebotomy. Conclusions Allospecific CD154+T-cytotoxic memory cells predict acute cellular rejection after LTx or ITx in children. Adjunctive use can enhance clinical outcomes. Recipient CD154+T-cytotoxic memory cells induced by stimulation with donor cells can be expressed as an immunoreactivity index determined by the fraction of those induced by HLA-non-identical cells in parallel cultures results, that if > 1, implies increased rejection risk in children with liver or intestine transplants." @default.
- W2326365518 created "2016-06-24" @default.
- W2326365518 creator A5003638648 @default.
- W2326365518 creator A5003961154 @default.
- W2326365518 creator A5006803861 @default.
- W2326365518 creator A5009504777 @default.
- W2326365518 creator A5013969602 @default.
- W2326365518 creator A5015944441 @default.
- W2326365518 creator A5023023016 @default.
- W2326365518 creator A5044296441 @default.
- W2326365518 creator A5045708158 @default.
- W2326365518 creator A5047888107 @default.
- W2326365518 creator A5047892291 @default.
- W2326365518 creator A5051741494 @default.
- W2326365518 creator A5054637743 @default.
- W2326365518 creator A5056242542 @default.
- W2326365518 creator A5060162359 @default.
- W2326365518 creator A5062737788 @default.
- W2326365518 creator A5068381719 @default.
- W2326365518 creator A5068590868 @default.
- W2326365518 creator A5072501231 @default.
- W2326365518 creator A5077060343 @default.
- W2326365518 creator A5084439610 @default.
- W2326365518 creator A5085033763 @default.
- W2326365518 creator A5086093973 @default.
- W2326365518 creator A5087293366 @default.
- W2326365518 creator A5089711857 @default.
- W2326365518 date "2017-01-01" @default.
- W2326365518 modified "2023-09-26" @default.
- W2326365518 title "Predicting Cellular Rejection With a Cell-Based Assay" @default.
- W2326365518 cites W1493858831 @default.
- W2326365518 cites W1523479931 @default.
- W2326365518 cites W1602160603 @default.
- W2326365518 cites W1813961098 @default.
- W2326365518 cites W1905555899 @default.
- W2326365518 cites W2001163947 @default.
- W2326365518 cites W2005612330 @default.
- W2326365518 cites W2020850832 @default.
- W2326365518 cites W2062415781 @default.
- W2326365518 cites W2065603960 @default.
- W2326365518 cites W2068925363 @default.
- W2326365518 cites W2079463014 @default.
- W2326365518 cites W2082552355 @default.
- W2326365518 cites W2083256666 @default.
- W2326365518 cites W2092684975 @default.
- W2326365518 cites W2094199149 @default.
- W2326365518 cites W2144900441 @default.
- W2326365518 cites W2163721979 @default.
- W2326365518 cites W2166073925 @default.
- W2326365518 cites W2166588973 @default.
- W2326365518 cites W2171765804 @default.
- W2326365518 cites W2318917650 @default.
- W2326365518 doi "https://doi.org/10.1097/tp.0000000000001076" @default.
- W2326365518 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/5011025" @default.
- W2326365518 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/26950712" @default.
- W2326365518 hasPublicationYear "2017" @default.
- W2326365518 type Work @default.
- W2326365518 sameAs 2326365518 @default.
- W2326365518 citedByCount "27" @default.
- W2326365518 countsByYear W23263655182017 @default.
- W2326365518 countsByYear W23263655182018 @default.
- W2326365518 countsByYear W23263655182019 @default.
- W2326365518 countsByYear W23263655182020 @default.
- W2326365518 countsByYear W23263655182021 @default.
- W2326365518 countsByYear W23263655182022 @default.
- W2326365518 countsByYear W23263655182023 @default.
- W2326365518 crossrefType "journal-article" @default.
- W2326365518 hasAuthorship W2326365518A5003638648 @default.
- W2326365518 hasAuthorship W2326365518A5003961154 @default.
- W2326365518 hasAuthorship W2326365518A5006803861 @default.
- W2326365518 hasAuthorship W2326365518A5009504777 @default.
- W2326365518 hasAuthorship W2326365518A5013969602 @default.
- W2326365518 hasAuthorship W2326365518A5015944441 @default.
- W2326365518 hasAuthorship W2326365518A5023023016 @default.
- W2326365518 hasAuthorship W2326365518A5044296441 @default.
- W2326365518 hasAuthorship W2326365518A5045708158 @default.
- W2326365518 hasAuthorship W2326365518A5047888107 @default.
- W2326365518 hasAuthorship W2326365518A5047892291 @default.
- W2326365518 hasAuthorship W2326365518A5051741494 @default.
- W2326365518 hasAuthorship W2326365518A5054637743 @default.
- W2326365518 hasAuthorship W2326365518A5056242542 @default.
- W2326365518 hasAuthorship W2326365518A5060162359 @default.
- W2326365518 hasAuthorship W2326365518A5062737788 @default.
- W2326365518 hasAuthorship W2326365518A5068381719 @default.
- W2326365518 hasAuthorship W2326365518A5068590868 @default.
- W2326365518 hasAuthorship W2326365518A5072501231 @default.
- W2326365518 hasAuthorship W2326365518A5077060343 @default.
- W2326365518 hasAuthorship W2326365518A5084439610 @default.
- W2326365518 hasAuthorship W2326365518A5085033763 @default.
- W2326365518 hasAuthorship W2326365518A5086093973 @default.
- W2326365518 hasAuthorship W2326365518A5087293366 @default.
- W2326365518 hasAuthorship W2326365518A5089711857 @default.
- W2326365518 hasBestOaLocation W23263655182 @default.
- W2326365518 hasConcept C105795698 @default.
- W2326365518 hasConcept C126322002 @default.
- W2326365518 hasConcept C151956035 @default.
- W2326365518 hasConcept C154317977 @default.
- W2326365518 hasConcept C202751555 @default.