INCREASED PLASMA SOLUBLE ADHESION MOLECULES IN THROMBOTIC THROMBOCYTOPENIC PURPURA AND DISSEMINATED INTRAVASCULAR COAGULATION

Citation
M. Shimura et al., INCREASED PLASMA SOLUBLE ADHESION MOLECULES IN THROMBOTIC THROMBOCYTOPENIC PURPURA AND DISSEMINATED INTRAVASCULAR COAGULATION, Clinical and applied thrombosis/hemostasis, 4(3), 1998, pp. 196-200
Citations number
24
Categorie Soggetti
Hematology
ISSN journal
10760296
Volume
4
Issue
3
Year of publication
1998
Pages
196 - 200
Database
ISI
SICI code
1076-0296(1998)4:3<196:IPSAMI>2.0.ZU;2-M
Abstract
We measured plasma-soluble adhesion molecules (granule membrane protei n [GMP]-140, endothelial leukocyte adhesion molecule [ELAM]-1. intrace llular adhesion molecule [ICAM]-1, and vascular adhesion molecule [VCA M]-1) in 21 patients with thrombotic thrombocytopenic purpura (TTP), 1 0 with mitomycin C-induced hemolytic uremic syndrome (MMC-HUS) and 59 with disseminated intravascular coagulation (DIC) or pre-DIC. The plas ma levels of soluble GMP-140 in the three groups were significantly hi gher than the levels in healthy volunteers, suggesting that platelets and vascular endothelial cells are activated in these diseases. The pl asma-soluble GMP-140 level of the DIC patients with nonhematopoietic m alignancy was significantly higher than in the DIC patients with hemat opoietic malignancy, perhaps due to the release of GMP-140 mainly from platelets. The plasma levels of soluble VCAM-1 in the TTP and DIC pat ients were significantly higher than the levels in healthy volunteers. The plasma levels of ICAM-1 in DIC patients were significantly higher than those in healthy volunteers, but the levels in the TTP and MMC-H US groups were not significantly high. The plasma ELAM-1 levels in the TTP and MMC-HUS groups were significantly lower than those in healthy volunteers and DIC patients. Since elevated plasma cytokine levels ha ve been observed in TTP and DIC patients, the adhesion molecules might be upregulated in these diseases. However, plasma ELAM-1 is thought t o be reduced in severe vascular endothelial cell diseases such as TTP.