ANTIBODIES TO PROTHROMBIN IN ANTIPHOSPHOLIPID SYNDROME AND INFLAMMATORY DISORDERS

Citation
J. Guerin et al., ANTIBODIES TO PROTHROMBIN IN ANTIPHOSPHOLIPID SYNDROME AND INFLAMMATORY DISORDERS, British Journal of Haematology, 102(4), 1998, pp. 896-902
Citations number
27
Categorie Soggetti
Hematology
ISSN journal
00071048
Volume
102
Issue
4
Year of publication
1998
Pages
896 - 902
Database
ISI
SICI code
0007-1048(1998)102:4<896:ATPIAS>2.0.ZU;2-#
Abstract
Antiphospholipid antibodies associated with the antiphospholipid syndr ome (APS) have been shown to bind plasma proteins, particularly beta 2 -glycoprotein I(beta 2-GPI), In this study the incidence of antibodies to solid-phase pro thrombin was examined in patients with antiphospho lipid syndrome and a variety of other inflammatory disorders. Signific antly elevated levels of IgG anti-prothrombin (anti-PT) antibodies wer e detected in 63% of patients with APS (n = 27, median 22 arbitrary un its: AU), 33% with SLE (n = 92, median 14 AU), 45% with rheumatoid fac tor (n = 22, median 16 AU), 21% with carotid artery stenosis (n = 21, median 15 AU), 32% with stroke (n = 38, median 13 AU), 67% of patients with a false positive serology for syphilis (n = 21, median 24 AU), 3 7% with HIV (n = 30, median 14 AU), 29% with syphilis (n = 14, median 19 AU) and 3% with infectious mononucleosis (n = 30, median 9 AU). In addition, a group of lupus anticoagulant (LA) positive patients (n = 4 8) was examined for antibodies to prothrombin, beta 2-GPI and cardioli pin. 10 (21%) patients had raised levels of IgG anti-PT antibodies, 30 (62%) had significantly elevated levels of anti-beta 2-GPI antibodies and 15 (31%) had elevated levels of anticardiolipin antibodies (ACA). Of the LA-positive patients, 15 (43%) were identified with definite A PS, eight (23%) with probable APS, two (6%) with possible APS and 10 ( 28%) patients had no clinical evidence of APS. In conclusion, antibodi es to prothrombin were found in a variety of inflammatory disorders an d were therefore not specific for the APS. However, identification of the plasma proteins recognized by antibodies from patients with APS ma y provide insight into the pathogenic mechanisms involved in the heter ogenous clinical manifestations of the APS.