Thromb Haemost 2006; 95(01): 68-76
DOI: 10.1160/TH05-05-0361
Blood Coagulation, Fibrinolysis and Cellular Haemostasis
Schattauer GmbH

Improved coagulation in bleeding disorders by Non-Anticoagulant Sulfated Polysaccharides (NASP)

Tongyao Liu
1   Avigen, Inc., Alameda, California
,
Ciaran D. Scallan
1   Avigen, Inc., Alameda, California
,
George J. Broze Jr.
2   Barnes-Jewish Hospital, Washington University School of Medicine, St. Louis, Missouri, USA
,
Susanna Patarroyo-White
1   Avigen, Inc., Alameda, California
,
Glenn F. Pierce
1   Avigen, Inc., Alameda, California
,
Kirk W. Johnson
1   Avigen, Inc., Alameda, California
› Author Affiliations
Further Information

Publication History

Received 24 May 2005

Accepted after revision 01 November 2005

Publication Date:
28 November 2017 (online)

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Summary

Additional therapeutic options are needed for patients with bleeding disorders such as hemophilia A, hemophilia B, severe von Willebrand disease, and other rare factor deficiencies. A novel approach to improve coagulation in such clotting disorders has been identified that, parodoxically, involves heparinlike sulfated polysaccharides.Select molecules of this broad class are largely devoid of anticoagulant activity and are here denoted Non-Anticoagulant Sulfated Polysaccharides (NASPs).A mechanism involving blockade of the extrinsic pathway downregulator,Tissue Factor Pathway Inhibitor (TFPI) by NASPs, was conceived as an approach for improving procoagulant behavior in hemophilic settings.A subset of NASPs, including pentosan polysulfate (PPS) and fucoidan inhibited both full-length and Kunitz 1 and 2 (K1K2) TFPI and, at concentrations from 4-500 nM, improved (i.e. accelerated) the clotting time of human hemophilia A and hemophilia B plasmas or plasma with reduced factor VII levels when tested in dilute prothrombin time (dPT) assays. Fucoidan did not reduce normal plasma APTT times implying specificity for extrinsic pathway control. Improved hemostasis in vivo was observed in mice with hemophilias A orB following low dose subcutaneous administration of PPS or fucoidan, or a combination of NASP plus factor supplement. Increased survival of factor deficient mice following a bleeding challenge was observed. Accordingly, administration of select NASP(s), via mechanism(s) not fully understood, represents a unique means of improving coagulation in bleeding disorders.