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Inhibition of Thrombin Abrogates the Instant Blood-Mediated Inflammatory Reaction Triggered by Isolated Human Islets: Possible application of the thrombin inhibitor melagatran in clinical islet transplantation
Rudbeck Laboratory, University Hospital, Uppsala.
Högskolan i Kalmar, Naturvetenskapliga institutionen. Rudbeck Laboratory, University Hospital, Uppsala.ORCID-id: 0000-0001-7888-1571
Rudbeck Laboratory, University Hospital, Uppsala.
Rudbeck Laboratory, University Hospital, Uppsala.
Vise andre og tillknytning
2002 (engelsk)Inngår i: Diabetes, ISSN 0012-1797, E-ISSN 1939-327X, Vol. 51, nr 6, s. 1779-1784Artikkel i tidsskrift (Fagfellevurdert) Published
Abstract [en]

A thrombotic/inflammatory reaction is elicited when isolated islets of Langerhans come in contact with ABO-compatible blood. The detrimental effects of this instant blood-mediated inflammatory reaction (IBMIR) provide a reasonable explanation for the observation that an unexpectedly high number of islets, from several donors, are needed to produce normoglycemia in transplant patients with type 1 diabetes. In this study, the hypothesis that a specific thrombin inhibitor, Melagatran, could reduce IBMIR in an in vitro model in which human islets are exposed to ABO-compatible blood was tested. The administration of Melagatran abrogated IBMIR dose-dependently. Islets exposed to blood, in the absence or presence of 0.4 μmol/l Melagatran, exhibited a loss of integrity and were found to be trapped in macroscopic clots containing platelets and CD11b+ leukocytes. At concentrations from 1 to 10 μmol/l, Melagatran inhibited both coagulation and complement activation. Also, platelet and leukocyte activation and consumption were decreased. Islet morphology was maintained with almost no platelets adhering to the surface, and infiltration by CD11b+ leukocytes was considerably reduced. In conclusion, Melagatran significantly reduced IBMIR in this model system. This protective effect indicates that thrombin plays a pivotal role in IBMIR and suggests that thrombin inhibition can improve the outcome of clinical islet transplantation.

sted, utgiver, år, opplag, sider
2002. Vol. 51, nr 6, s. 1779-1784
HSV kategori
Forskningsprogram
Biomedicinsk vetenskap, Immunologi
Identifikatorer
URN: urn:nbn:se:lnu:diva-1149DOI: 10.2337/diabetes.51.6.1779OAI: oai:DiVA.org:lnu-1149DiVA, id: diva2:307938
Tilgjengelig fra: 2010-04-01 Laget: 2010-04-01 Sist oppdatert: 2018-01-12bibliografisk kontrollert

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