Thromb Haemost 2013; 109(05): 901-908
DOI: 10.1160/TH12-03-0212
Blood Coagulation, Fibrinolysis and Cellular Haemostasis
Schattauer GmbH

Platelet and endothelial activation in catastrophic and quiescent antiphospholipid syndrome

Agnese Bontadi
1   Rheumatology Unit, Department of Medicine, University of Padua, Padua, Italy
,
Amelia Ruffatti
1   Rheumatology Unit, Department of Medicine, University of Padua, Padua, Italy
,
Emanuela Falcinelli
2   Division of Internal and Cardiovascular Medicine, Department of Internal Medicine, University of Perugia, Perugia, Italy
,
Silvia Giannini
2   Division of Internal and Cardiovascular Medicine, Department of Internal Medicine, University of Perugia, Perugia, Italy
,
Alessandro Marturano
2   Division of Internal and Cardiovascular Medicine, Department of Internal Medicine, University of Perugia, Perugia, Italy
,
Marta Tonello
1   Rheumatology Unit, Department of Medicine, University of Padua, Padua, Italy
,
Ariela Hoxha
1   Rheumatology Unit, Department of Medicine, University of Padua, Padua, Italy
,
Vittorio Pengo
3   Clinical Cardiology, Thrombosis Centre, University of Padua, Padua, Italy
,
Leonardo Punzi
1   Rheumatology Unit, Department of Medicine, University of Padua, Padua, Italy
,
Stefania Momi
2   Division of Internal and Cardiovascular Medicine, Department of Internal Medicine, University of Perugia, Perugia, Italy
,
Paolo Gresele
2   Division of Internal and Cardiovascular Medicine, Department of Internal Medicine, University of Perugia, Perugia, Italy
› Author Affiliations
Further Information

Publication History

Received: 02 April 2012

Accepted after major revision: 17 February 2013

Publication Date:
22 November 2017 (online)

Summary

Antiphospholipid antibodies (aPL) seem to induce a prothrombotic state by activating endothelium and platelets, but no studies have evaluated systematically the effects of aPL from patients with the antiphospholipid syndrome (APS) in quiescent versus catastrophic phase. Our aims were to evaluate the in vitro effects on platelet activation of anti-β2 glycoprotein I (anti-β2GPI) antibodies isolated from APS patient in either quiescent or catastrophic phase and to investigate ex vivo platelet and endothelial activation in patients with quiescent or catastrophic APS. Anti-β2GPI antibodies were isolated from plasma of a pregnant woman in two different stages of APS (quiescent and catastrophic, respectively). They were co-incubated with washed platelets from healthy controls that were then challenged with TRAP-6 (thrombin receptor activating peptide 6) and the expression of P-selectin (P-sel) on platelets was assessed by flow cytometry. Moreover, plasma samples from six patients with quiescent, four with catastrophic APS and 10 controls were assessed for several markers of platelet and endothelial activation. The results showed that purified anti-β2GPI antibodies co-incubated with platelets enhanced TRAP-6-induced platelet P-sel expression. Notably, anti-β2GPI antibodies isolated during the catastrophic phase enhanced platelet P-sel expression more than antibodies isolated from the same patient in the quiescent stage of disease. Moreover, APS patients had significantly higher plasma levels of soluble (s) Psel, sCD40 ligand, soluble vascular cell adhesion molecule 1 and monocyte chemoattractant protein 1 than control subjects. In addition, sP-sel and von Willebrand factor activity were significantly higher during catastrophic than in quiescent phase.

 
  • References

  • 1 Miyakis S, Lockshin MD, Atsumi T, et a. International consensus statement on an update of the classification criteria for definite antiphospholipid syndrome (APS). J Thromb Haemost 2006; 04: 295-306.
  • 2 Levine JS, Branch DW, Rauch J. The antiphospholipid syndrome. N Engl J Med 2002; 346: 752-763.
  • 3 Cervera R, Piette JC, Font J. et al. Antiphospholipid syndrome: clinical and immunologic manifestations and patterns of disease expression in a cohort of 1,000 patients. Arthritis Rheum 2002; 46: 1019-1027.
  • 4 Asherson RA, Cervera R, de Groot PG. et al. Catastrophic antiphospholipid syndrome: international consensus statement on classification criteria and treatment guidelines. Lupus 2003; 12: 530-534.
  • 5 Bortolati A, Marson P, Fabris F. et al. Recovery from catastrophic antiphospholipid syndrome by a plasma exchange procedure: report of four cases and review of the literature Autoimmunity. Reviews 2009; 08: 297-301.
  • 6 Asherson RA, Cervera R, Piette JC. et al. Catastrophic antiphospholipid syndrome: clues to the pathogenesis from a series of 80 patients. Medicine 2001; 80: 355-377.
  • 7 Asherson RA, Cervera R, Piette JC. et al. Catastrophic antiphospholipid syndrome. Clinical and laboratory features of 50 patients. Medicine 1998; 77: 195-207.
  • 8 Bucciarelli S, Espinosa G, Cervera R. et al. Mortality in the catastrophic antiphospholipid syndrome: causes of death and prognostic factors in a series of 250 patients. Arthritis Rheum 2006; 54: 2568-2576.
  • 9 Salmon JE, de Groot PG. Pathogenic role of antiphospholipid antibodies. Lupus 2008; 17: 405-411.
  • 10 Font J, Espinosa G, Tàssies D. et al. Effects of beta2-glycoprotein I and monoclonal anticardiolipin antibodies in platelet interaction with subendothelium under flow conditions. Arthritis Rheum 2002; 46: 3283-3289.
  • 11 Galli M, Comfurius P, Maassen C. et al. Anticardiolipin antibodies (ACA) directed not to cardiolipin but to a plasma protein cofactor. Lancet 1990; 335: 1544-1547.
  • 12 Hunt JE, Simpson RJ, Krilis SA. Identification of a region of beta 2-glycoprotein I critical for lipid binding and anti-cardiolipin antibody cofactor activity. Proc Natl Acad Sci USA 1993; 90: 2141-2145.
  • 13 McNeil HP, Simpson RJ, Chesterman CN. et al. Anti-phospholipid antibodies are directed against a complex antigen that includes a lipid-binding inhibitor of coagulation: beta 2-glycoprotein I (apolipoprotein H). Proc Nat Acad Sciences USA 1990; 87: 4120-4124.
  • 14 Agar C, van Os GM, Morgelin M. et al. {beta}2-Glycoprotein I can exist in two conformations: implications for our understanding of the antiphospholipid syndrome. Blood 2010; 116: 1336-1343.
  • 15 Koike T, Ichikawa K, Kasahara H. et al. Epitopes on beta2-GPI recognized by anticardiolipin antibodies. Lupus 1998; 07 (Suppl. 02) S14-17.
  • 16 Pennings MT, Derksen RH, van Lummel M. et al. Platelet adhesion to dimeric beta2-glycoprotein-I under conditions of flow is mediated by at least two receptros: glycoprotein Ibalpha and APOER2’. J Thromb Haemost 2007; 05: 369-377.
  • 17 Shi T, Giannakopoulos B, Yan X. et al. Anti-β2-glycoprotein I antibodies in complex with β2-glycoprotein I can activate platelets in a dysregulated manner via glycoprotein Ib-IX-V. Arthritis Rheum 2006; 54: 2558-2567.
  • 18 Urbanus RT, Pennings MT, Derksen RHWM. et al. Platelet activation by dimeric β2-glycoprotein I requires signalling via both glycoprotein Ibα and apoliprotein E receptor 2’. J Thromb Haemost 2008; 06: 1405-1412.
  • 19 Urbanus RT, Derksen RH, de Groot PG. Platelets and the antiphospholipid syndrome. Lupus 2008; 17: 888-894.
  • 20 Vlachoyiannopoulos PG, Routsias JG. A novel mechanism of thrombosis in antiphospholipid antibody syndrome. J Autoimmun 2010; 35: 248-255.
  • 21 Robbins DL, Leung S, Miller-Blair DJ. et al. Effect of anticardiolipin/beta2-glycoprotein I complexes on production of thromboxane A2 by platelets from patients with the antiphospholipid syndrome. J Rheumatol 1998; 25: 51-56.
  • 22 Lin YL, Wang CT. Activation of human platelets by the rabbit anticardiolipin antibodies. Blood 1992; 80: 3135-3143.
  • 23 Berlacher MD, Vieth JA, Heflin BC. et al. FcγRIIa Ligation Induces Platelet Hypersensitivity to Thrombotic Stimuli. Am J Pathol 2013; 182: 244-254.
  • 24 Pierangeli SS, Colden-Stanfield M, Liu X. et al. Antiphospholipid antibodies from antiphospholipid syndrome patients activate endothelial cells in vitro and in vivo. Circulation 1999; 99: 1997-2002.
  • 25 Simantov R, La Sala JM, Lo SK. et al. Activation of cultured vascular endothelial cells by antiphospholipid antibodies. J Clin Invest 1995; 96: 2211-2219.
  • 26 Hulstein JJ, Lenting PJ, de Laat B. et al. Beta2-glycoprotein I inhibits von Wille-brand factor dependent platelet adhesion and aggregation. Blood 2007; 110: 1483-1491.
  • 27 Pengo V, Brocco T, Biasiolo A. et al. Procoagulant effect of anti-beta2-glycoprotein I antibodies with lupus anticoagulant activity. Blood 1999; 94: 3814-3819.
  • 28 Tincani A, Allegri F, Balestrieri G. et al. Minimal requirements for antiphospholipid antibodies ELISAs proposed by the European Forum on antiphospholipid antibodies. Thromb Res 2004; 114: 553-558.
  • 29 Rossiello MR, Momi S, Caracchini R. et al. A novel nitric oxide-releasing statin derivative exerts an antiplatelet/antithrombotic activity and inhibits tissue factor expression. J Thromb Haemost 2005; 03: 2554-2562.
  • 30 Ciferri S, Emiliani C, Guglielmini G. et al. Platelets release their lysosomal content in vivo in humans upon activation. Thromb Haemost 2000; 83: 157-164.
  • 31 Falcinelli E, Guglielmini G, Torti M. et al. Intraplatelet signalling mechanisms of the priming effect of matrix metalloproteinase-2 on platelet aggregation. J Thromb Haemost 2005; 03: 2526-2535.
  • 32 Takai T, Li M, Sylvestre D. et al. FcRγ chain deletion results in pleiotropic effector cell defects. Cell 1994; 76: 519-529.
  • 33 Momi S, Falcinelli E, Giannini S. et al. Loss of matrix metalloproteinase 2 in platelets reduces arterial thrombosis in vivo. J Exp Med 2009; 206: 2365-2379.
  • 34 Giannini S, Falcinelli E, Bury L. et al. Interaction with damaged vessel wall in vivo in humans induces platelets to express CD40L resulting in endothelial activation with no effect of aspirin intake. Am J Physiol Heart Circ Physiol 2011; 300: H2072-2079.
  • 35 Francisci D, Giannini S, Baldelli F. et al. HIV type 1 infection, and not short-term HAART, induces endothelial dysfunction. AIDS 2009; 23: 589-596.
  • 36 Giannini S, Mezzasoma AM, Leone M. et al. Laboratory diagnosis and monitoring of desmopressin treatment of von Willebrand’s disease by flow cytometry. Haematologica 2007; 92: 1647-1654.
  • 37 Cucnik S, Kveder T, Krizaj I. et al. High avidity anti-β2-glycoprotein I antibodies in patients with antiphospholipid syndrome. Ann Rheum Dis 2004; 63: 1478-1482.
  • 38 Bozic B, Cucnik S, Kveder T. et al. Changes in avidity and specificity of IgG during electro-oxidation. Relevance of binding of antibodies to β2-GPI. Autoimmun Rev 2006; 06: 28-32.
  • 39 Cucnik S, Kveder T, Ulcova GZ. et al. The avidity of anti-beta2-glycoprotein I antibodies in patients with or without antiphospholipid syndrome: a collaborative study in the frame of the European forum on antiphospholipid antibodies. Lupus 2011; 20: 1166-1171.
  • 40 Žager U, Irman Š, Lunder M. et al. Immunochemical properties and pathological relevance of anti-β2-glycoprotein I antibodies of different avidity. Int Immunol 2011; 23: 511-518.
  • 41 George J, Blank M, Levy Y. et al. Differential effects of anti-beta2-glycoprotein I antibodies on endothelial cells and on the manifestations of experimental antiphospholipid syndrome. Circulation 1998; 97: 900-906.
  • 42 Banzato A, Frasson R, Acquasaliente L. et al. Circulating b2 glycoprotein I-IgG anti-b2 glycoprotein Iimmunocomplexes in patients with definite Antiphospholipid Syndrome. Lupus 2012; 21: 784-786.