SPECIFIC ANTIPLATELET AUTOANTIBODIES IN PATIENTS WITH ANTIPHOSPHOLIPID ANTIBODIES AND THROMBOCYTOPENIA

Citation
F. Fabris et al., SPECIFIC ANTIPLATELET AUTOANTIBODIES IN PATIENTS WITH ANTIPHOSPHOLIPID ANTIBODIES AND THROMBOCYTOPENIA, European journal of haematology, 53(4), 1994, pp. 232-236
Citations number
21
Categorie Soggetti
Hematology
ISSN journal
09024441
Volume
53
Issue
4
Year of publication
1994
Pages
232 - 236
Database
ISI
SICI code
0902-4441(1994)53:4<232:SAAIPW>2.0.ZU;2-9
Abstract
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.