RANTES and MCP-1 chemokine plasma levels in chronic renal transplant dysfunction and chronic renal failure

被引:28
作者
Corsi, MM
Leone, G
Fulgenzi, A
Wasserman, K
Leone, F
Ferrero, ME
机构
[1] Institute of General Pathology, Fac. of Med., University of Milan, Milan
[2] C.N.R. Center for Cellular Pathology, Milan
[3] First Clinical Surgery, Fac. of Med., University of Catania, Catania
[4] Nuclear Medicine Department, IRCCS Ospedale Maggiore, Milan
[5] Lab. of Experimental Immunology, Div. of Basic Sciences, NCI FCRDC, Frederick, MD
[6] Transplant Surgery, Fac. of Med., University of Catania, Catania
关键词
RANTES; MCP-1; kidney transplantation; chronic dysfunction;
D O I
10.1016/S0009-9120(99)00038-7
中图分类号
R446 [实验室诊断]; R-33 [实验医学、医学实验];
学科分类号
1001 ;
摘要
Objectives: Procedures to diagnose renal allograft rejection depend on detection of graft dysfunction due to the presence of mononuclear leukocytic infiltrates. Design and methods: In our study, we pursued an immunodiagnostic approach utilizing an ELISA method on plasma samples to monitor patients waiting to undergo transplantation in order to evidence prognostic developments in renal transplantation and, at least, to diagnose renal chronic transplant dysfunction. We analyzed blood levels of two chemokines, RANTES and MCP-1, which are normally overexpressed locally in renal chronic rejection. Results: Our results showed that patients affected by chronic renal failure (and waiting for kidney transplant), as well as kidney-grafted patients affected by chronic transplant dysfunction, had plasma levels of RANTES significantly higher than those of controls (patients without acute or chronic pathologies). Conclusions: Our data suggest a simple method to evaluate the plasmatic presence of RANTES, which could be involved in longterm kidney graft failure. Copyright (C) 1999 The Canadian Society of Clinical Chemists.
引用
收藏
页码:455 / 460
页数:6
相关论文
共 28 条
[1]   Hepatic expression of macrophage inflammatory protein-1 alpha and macrophage inflammatory protein-1 beta after liver transplantation [J].
Adams, DH ;
Hubscher, S ;
Fear, J ;
Johnston, J ;
Shaw, S ;
Afford, S .
TRANSPLANTATION, 1996, 61 (05) :817-825
[2]  
ADAMS DH, 1989, TRANSPLANT REV, V3, P131
[3]   Intragraft cytokine gene expression: implications for clinical transplantation [J].
Baan, CC ;
Weimar, W .
TRANSPLANT INTERNATIONAL, 1998, 11 (03) :169-180
[4]   Chemokines and leukocyte traffic [J].
Baggiolini, M .
NATURE, 1998, 392 (6676) :565-568
[5]   Chemokine sequestration by viral chemoreceptors as a novel viral escape strategy: Withdrawal of chemokines from the environment of cytomegalovirus-infected cells [J].
Bodaghi, B ;
Jones, TR ;
Zipeto, D ;
Vita, C ;
Sun, L ;
Laurent, L ;
Arenzana-Seisdedos, F ;
Virelizier, JL ;
Michelson, S .
JOURNAL OF EXPERIMENTAL MEDICINE, 1998, 188 (05) :855-866
[6]   MONOCYTE CHEMOATTRACTANT PROTEIN-1 ACTS AS A T-LYMPHOCYTE CHEMOATTRACTANT [J].
CARR, MW ;
ROTH, SJ ;
LUTHER, E ;
ROSE, SS ;
SPRINGER, TA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1994, 91 (09) :3652-3656
[7]  
CRIMM PC, 1995, J AM SOC NEPHROL, V6, P1057
[8]  
DALMANN MJ, 1993, CURR OPIN IMMUNOL, V5, P788
[9]  
Gjertson D W, 1991, Clin Transpl, P225
[10]  
Grandaliano G, 1997, TRANSPLANTATION, V63, P414, DOI 10.1097/00007890-199702150-00015