We have quantified levels of CD105, its ligand TGF beta and receptor-ligand
complexes in sera from healthy individuals (n = 31), patients with triple
vessel disease documented by coronary angiography (TVD; n = 36) and patient
s with chest pain and a positive exercise electrocardiogram but with normal
coronary angiogram (NCA; n = 30). Both active TGF beta 1 and active plus a
cid-activatable TGF beta 1 [(a + 1)TGF beta 1] were significantly depressed
in patients with TVD compared with the other two groups (P less than or eq
ual to 0.04). CD105 levels in TVD patients were also diminished but elevate
d in NCA patients. In contrast, patients with TVD had more CD105/TGF beta 1
complex in their sera than the other two groups, suggesting that this may
be the reason why TVD patients had low levels of receptor and ligand. TGF b
eta 3 levels were similar in the three groups, but elevated CD105/TGF beta
3 levels were noted in patients with NCA compared with those with TVD and h
ealthy individuals (P less than or equal to 0.02). CD105 was correlated wit
h both active TGF beta 1 and (a + 1)TGF beta 1 (P = 0.02). CD105 also stron
gly correlated with TGF beta 3 and CD105/TGF beta 3 complexes (P = 0.001 in
both cases). The changes in levels of CD105, TGF beta 1 and the receptor-l
igand complexes in sera of patients with atherosclerosis suggest that these
molecules may be important in the pathobiology of the atherosclerotic dise
ase. Further studies on sequential samples from a larger cohort of patients
are needed to define a causal relationship between these molecules and the
disease progression. (C) 2000 Elsevier Science Ireland Ltd. All rights res
erved.