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DOI 10.1016/j.trim.2006.08.002

Медицинская библиотека · Transplant immunology · 2006

Circulating adhesion molecules during kidney allograft reperfusion.

Domański L, Gryczman M, Pawlik A, Sulikowski M, Romanowski M, Ostrowski M, Myślak M, Rózański J, Safranow K, Dutkiewicz G, Ciechanowski K

СтатьяПоддержка исследования: вне правительства СШАПеревод в очереди

Аннотация

Adhesion molecule expression is an important event during early transplant failure. The aim of the present study was to examine the release of adhesion molecules during the first minutes of kidney allograft reperfusion in relation to delayed graft function and acute graft rejection. We enrolled 49 renal transplant recipients, including 13 cases of delayed graft function (DGF) and 11 cases of acute graft rejection (AR). Plasma concentrations of E-selectin, VCAM-1 and ICAM-1 after 3 min of reperfusion were significantly higher than in the iliac vein before reperfusion. There was no statistically significant difference between patients with and without DGF as regards E-selectin, VCAM-1 and ICAM-1 concentrations in the iliac vein before and in the renal vein after 3 min of reperfusion. Concentrations of adhesion molecules in the iliac vein before reperfusion and in the renal vein after 3 min of reperfusion did not differ significantly between patients with and without AR except for ICAM-1 iliac vein concentration which was significantly increased in AR patients. Plasma levels of E-selectin, ICAM-1 and VCAM-1 were increased after kidney allograft reperfusion. Moreover, elevated serum levels of ICAM-1 before transplantation correlated with subsequent acute kidney allograft rejection. The results suggest that elevated ICAM-1 levels may be implicated in acute graft rejection.

Для цитирования: Domański L, Gryczman M, Pawlik A, Sulikowski M, Romanowski M, Ostrowski M, Myślak M, Rózański J, Safranow K, Dutkiewicz G, Ciechanowski K. Circulating adhesion molecules during kidney allograft reperfusion.. Transplant immunology. 2006. DOI: 10.1016/j.trim.2006.08.002.

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