F. Fabris et al., SPECIFIC ANTIPLATELET AUTOANTIBODIES IN PATIENTS WITH ANTIPHOSPHOLIPID ANTIBODIES AND THROMBOCYTOPENIA, European journal of haematology, 53(4), 1994, pp. 232-236
By means of immunoblotting and monoclonal antibody immobilization of p
latelet antigens (MAIPA) we have studied the specificity of antiplatel
et antibodies in patients with antiphospholipid antibodies and thrombo
cytopenia defined as presence of anticardiolipin IgG and a platelet co
unt below 100 x 10(9)/l. The study group consisted of 10 patients with
systemic lupus erythematosus (SLE), 8 patients with primary anti-phos
pholipid syndrome (PAPS) and 16 patients with idiopathic thrombocytope
nic purpura (ITP). The comparison group was formed by 17 patients with
classical chronic ITP without anticardiolipin IgG. We identified the
80-100, 130-150 and 150-170 KD surface proteins that comigrate with GP
IIIa, GPIIb and GPIb and a 50-70 KD cytoplasm band by immunoblot. In p
atients with classical chronic ITP, the prevalence of the antiplatelet
antibodies against GPIIIa was 53% on immunoblot assay and 47% on MAIP
A. In ITP patients who had also anti-phospholipid antibodies in serum,
the percentage of reactivity to GPIIIa declined to 37% on immunoblot
and 21% on MAIPA but it was not statistically different from the perce
ntage observed in patients with classical ITP. Autoantibodies to plate
let surface glycoproteins were almost absent in SLE and PAPS patients,
who showed a significant prevalence (78%) of IgG reactivity to the 50
-70 KD internal platelet protein which was frequently encountered also
in patients with ITP and aPL (56%). Our study provides additional evi
dence that platelet antigens in patients with phospholipid-associated
secondary immune thrombocytopenia are different from those of primary
ITP, and that surface glycoproteins were not involved.