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Clinical islet isolation outcomes with a highly purified neutral protease for pancreas dissociation
Background: Pancreas dissociation is a critical initial component of the islet isolation procedure and introduces high variability based on factors including the enzyme type, specificity and potency. Product refinement and alterations to the application strategies have improved isolation outcomes ov...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Landes Bioscience
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4049837/ https://www.ncbi.nlm.nih.gov/pubmed/23756701 http://dx.doi.org/10.4161/isl.25222 |
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author | O'Gorman, Doug Kin, Tatsuya Pawlick, Rena Imes, Sharleen Senior, Peter A Shapiro, AM James |
author_facet | O'Gorman, Doug Kin, Tatsuya Pawlick, Rena Imes, Sharleen Senior, Peter A Shapiro, AM James |
author_sort | O'Gorman, Doug |
collection | PubMed |
description | Background: Pancreas dissociation is a critical initial component of the islet isolation procedure and introduces high variability based on factors including the enzyme type, specificity and potency. Product refinement and alterations to the application strategies have improved isolation outcomes over time; however, islet utilization from donor organs remains low. In this study we evaluate a low endotoxin-high activity grade neutral protease in clinical islet isolation. Materials and Methods: The use of a non-collagenolytic enzyme, either thermolysin or high active neutral protease, was randomized in clinical islet isolations to evaluate efficacy. Additionally a retrospective comparison to neutral protease NB was conducted. Results:The thermolysin group had lower trapped islet population and increased purity and post-culture islet mass in comparison to high active grade neutral protease. Comparison of neutral protease NB GMP grade to high active neutral protease displayed no measurable difference in islet mass or viability and transplantation outcomes at 1 mo post-transplant were favorable for both groups. Conclusions: High activity neutral protease can generate clinical grade islets and may prove beneficial to islet function and viability based on a reduced endotoxin load but dosing of neutral protease requires ongoing optimization. |
format | Online Article Text |
id | pubmed-4049837 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Landes Bioscience |
record_format | MEDLINE/PubMed |
spelling | pubmed-40498372014-06-25 Clinical islet isolation outcomes with a highly purified neutral protease for pancreas dissociation O'Gorman, Doug Kin, Tatsuya Pawlick, Rena Imes, Sharleen Senior, Peter A Shapiro, AM James Islets Research Paper Background: Pancreas dissociation is a critical initial component of the islet isolation procedure and introduces high variability based on factors including the enzyme type, specificity and potency. Product refinement and alterations to the application strategies have improved isolation outcomes over time; however, islet utilization from donor organs remains low. In this study we evaluate a low endotoxin-high activity grade neutral protease in clinical islet isolation. Materials and Methods: The use of a non-collagenolytic enzyme, either thermolysin or high active neutral protease, was randomized in clinical islet isolations to evaluate efficacy. Additionally a retrospective comparison to neutral protease NB was conducted. Results:The thermolysin group had lower trapped islet population and increased purity and post-culture islet mass in comparison to high active grade neutral protease. Comparison of neutral protease NB GMP grade to high active neutral protease displayed no measurable difference in islet mass or viability and transplantation outcomes at 1 mo post-transplant were favorable for both groups. Conclusions: High activity neutral protease can generate clinical grade islets and may prove beneficial to islet function and viability based on a reduced endotoxin load but dosing of neutral protease requires ongoing optimization. Landes Bioscience 2013-05-01 2013-06-11 /pmc/articles/PMC4049837/ /pubmed/23756701 http://dx.doi.org/10.4161/isl.25222 Text en Copyright © 2013 Landes Bioscience http://creativecommons.org/licenses/by-nc/3.0/ This is an open-access article licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported License. The article may be redistributed, reproduced, and reused for non-commercial purposes, provided the original source is properly cited. |
spellingShingle | Research Paper O'Gorman, Doug Kin, Tatsuya Pawlick, Rena Imes, Sharleen Senior, Peter A Shapiro, AM James Clinical islet isolation outcomes with a highly purified neutral protease for pancreas dissociation |
title | Clinical islet isolation outcomes with a highly purified neutral protease for pancreas dissociation |
title_full | Clinical islet isolation outcomes with a highly purified neutral protease for pancreas dissociation |
title_fullStr | Clinical islet isolation outcomes with a highly purified neutral protease for pancreas dissociation |
title_full_unstemmed | Clinical islet isolation outcomes with a highly purified neutral protease for pancreas dissociation |
title_short | Clinical islet isolation outcomes with a highly purified neutral protease for pancreas dissociation |
title_sort | clinical islet isolation outcomes with a highly purified neutral protease for pancreas dissociation |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4049837/ https://www.ncbi.nlm.nih.gov/pubmed/23756701 http://dx.doi.org/10.4161/isl.25222 |
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