Source:http://linkedlifedata.com/resource/pubmed/id/14961992
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
3
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pubmed:dateCreated |
2004-2-13
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pubmed:abstractText |
We sought to determine whether or not optimizing pancreas preservation, islet processing, and induction immunosuppression would facilitate sustained diabetes reversal after single-donor islet transplants. Islets were isolated from two-layer preserved pancreata, purified, cultured for 2 days; and transplanted into six C-peptide-negative, nonuremic, type 1 diabetic patients with hypoglycemia unawareness. Induction immunosuppression, which began 2 days pretransplant, included the Fc receptor nonbinding humanized anti-CD3 monoclonal antibody hOKT3gamma1 (Ala-Ala) and sirolimus. Immunosuppression was maintained with sirolimus and reduced-dose tacrolimus. Of our six recipients, four achieved and maintained insulin independence with normal HbA1c levels and freedom from hypoglycemia; one had partial islet graft function; and one lost islet graft function 2 weeks post-transplant. The four insulin-independent patients showed prolonged CD4+ T-cell lymphocytopenia; inverted CD4:CD8 ratios; and increases in the percentage of CD4+CD25+ T cells. These cells suppressed the in-vitro proliferative response to donor cells and, to a lesser extent, to third-party cells. Severe adverse events were limited to a transient rash in one recipient and to temporary neutropenia in three. Our preliminary results thus suggest that a combination of maximized viable islet yield, pretransplant islet culture, and preemptive immunosuppression can result in successful single-donor islet transplants.
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pubmed:grant | |
pubmed:commentsCorrections | |
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 |
Mar
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pubmed:issn |
1600-6135
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pubmed:author |
pubmed-author:AnsiteJeffrey DJD,
pubmed-author:BluestoneJeffrey AJA,
pubmed-author:ClemmingsSue MSM,
pubmed-author:EckmanPeter MPM,
pubmed-author:HarmonJames VJV,
pubmed-author:HeringBernhard JBJ,
pubmed-author:KandaswamyRajaR,
pubmed-author:MatsumotoIppeiI,
pubmed-author:NakanoMasahikoM,
pubmed-author:ParaskevasStephenS,
pubmed-author:SageshimaJunichiroJ,
pubmed-author:SakaiTetsuyaT,
pubmed-author:SawadaToshiyaT,
pubmed-author:SutherlandDavid E RDE,
pubmed-author:ZhangHui JHJ
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pubmed:issnType |
Print
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pubmed:volume |
4
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
390-401
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pubmed:dateRevised |
2007-11-14
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pubmed:meshHeading |
pubmed-meshheading:14961992-Adult,
pubmed-meshheading:14961992-Antigens, CD3,
pubmed-meshheading:14961992-Diabetes Mellitus, Type 1,
pubmed-meshheading:14961992-Female,
pubmed-meshheading:14961992-Humans,
pubmed-meshheading:14961992-Islets of Langerhans,
pubmed-meshheading:14961992-Islets of Langerhans Transplantation,
pubmed-meshheading:14961992-Male,
pubmed-meshheading:14961992-Middle Aged,
pubmed-meshheading:14961992-Muromonab-CD3,
pubmed-meshheading:14961992-Pancreas,
pubmed-meshheading:14961992-T-Lymphocyte Subsets,
pubmed-meshheading:14961992-Tissue Donors
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pubmed:year |
2004
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pubmed:articleTitle |
Transplantation of cultured islets from two-layer preserved pancreases in type 1 diabetes with anti-CD3 antibody.
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pubmed:affiliation |
Diabetes Institute for Immunology and Transplantation, Department of Surgery, University of Minnesota, Minneapolis, MN, USA. bhering@umn.edu
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pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, P.H.S.,
Research Support, Non-U.S. Gov't
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