2004
DOI: 10.1016/j.transproceed.2004.06.001
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The role of current product release criteria for identification of human islet preparations suitable for clinical transplantation

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Cited by 27 publications
(23 citation statements)
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“…This is in accordance with the previous reports that most of the currently used methods for islet product release criteria were not able to foresee transplantation outcome (5)(6)(7)14).…”
Section: Discussionsupporting
confidence: 93%
“…This is in accordance with the previous reports that most of the currently used methods for islet product release criteria were not able to foresee transplantation outcome (5)(6)(7)14).…”
Section: Discussionsupporting
confidence: 93%
“…But partial thrombosis of portal vein branches (51) and, in the long-term, tissue remodeling and morphological alteration into the liver (13,52) have been described as complications of large tissue volume transplantation. In addition, in a univariate analysis, the islet purity level was directly correlated with the C-peptide value of recipients a month after transplant (12), although this was not confirmed by the multivariate analysis or other studies (12,53).…”
Section: Islet Preparation Compositionmentioning
confidence: 74%
“…This requirement has not been achieved, in part because the characteristics determined by currently accepted assay methods, individually or collectively, do not correlate with transplantation outcome. [2][3][4][5][6][7][8][9] Development of meaningful assays of islet properties is challenging for several reasons 8 : (1) Many techniques suitable for cells are not practical with islets because of their three-dimensional aggregate structure. Islets cannot be usefully dissociated into dispersed cells by agitation and incubation with serine proteases such as trypsin because from 30% to 50% of the cells are lost during dissociation.…”
Section: Introductionmentioning
confidence: 99%