The CD40-CD40L interaction, which was initially shown to have important rol
es in the T cell-mediated activation of B cells during humoral immune respo
nses, is now known to have roles in activation of endothelial cells, smooth
muscle cells, and macrophages within atherosclerotic plaques. Recently, CD
40L expression was found in activated platelets in the thrombus in vivo and
CD40L was reported to be responsible for the platelet-mediated activation
of endothelial cells in vitro, To investigate the activation status of plat
elets in coronary artery disease patients, we tested expression levels of C
D40L, and platelet-endothelial cell adhesion molecule-1 (PECAM-1/ CD31) in
platelets isolated from peripheral blood, using flow cytometric analysis, T
wenty-nine patients with acute coronary syndrome (10 acute myocardial infar
ction and 19 unstable angina patients) were compared with 14 normal subject
s or 14 stable angina patients, In platelets isolated from normal subjects,
the expression of CD40L was not detected in all subjects. In the patients
with acute coronary syndrome, the average level of CD40L showed a significa
nt increase (p = 0.0028), while stable angina patients did not have any inc
rease when compared to normal subjects. Patients with more complex lesions
or vessel occlusion tended to have a high platelet CD40L level compared to
patients who do not, The expression levels of CD31 were increased in a smal
l portion of the ACS patients. These data indicate that the rupture of plaq
ue and subsequent formation of thrombus may lead to the activation of CD40L
expression in circulating platelets of ACS patients. Copyright (C) 2000 S.
Karger AG, Basel.