Synthetic Pentasaccharides Do Not Cause Platelet Activation by Antiheparin-Platelet Factor 4 Antibodies

A synthetic selective inhibitor of factor Xa, the pentasaccharide SR90107A/Org31540 is in clinical develop ment for the prophylaxis of postsurgical deep vein thrombosis. Another synthetic pentasaccharide with even more sustained inhibition of factor Xa, SanOrg34006, has also been developed. Both of...

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Veröffentlicht in:Clinical and applied thrombosis/hemostasis 1999-10, Vol.5 (4), p.259-266
Hauptverfasser: Ahmad, Sarfraz, Jeske, Walter P., Walenga, Jeanine M., Hoppensteadt, Debra A., Wood, Jennifer J., Herbert, Jean-Marc, Messmore, Harry L., Fareed, Jawed
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container_end_page 266
container_issue 4
container_start_page 259
container_title Clinical and applied thrombosis/hemostasis
container_volume 5
creator Ahmad, Sarfraz
Jeske, Walter P.
Walenga, Jeanine M.
Hoppensteadt, Debra A.
Wood, Jennifer J.
Herbert, Jean-Marc
Messmore, Harry L.
Fareed, Jawed
description A synthetic selective inhibitor of factor Xa, the pentasaccharide SR90107A/Org31540 is in clinical develop ment for the prophylaxis of postsurgical deep vein thrombosis. Another synthetic pentasaccharide with even more sustained inhibition of factor Xa, SanOrg34006, has also been developed. Both of these agents were tested in comparison to unfraction ated heparin and a low molecular weight heparin (enoxaparin) for their relative platelet activation potential in heparin-induced thrombocytopenia assays. Sera from patients (n = 30) with heparin-induced thrombocytopenia were pooled and validated for heparin-dependent aggregation responses. Using heparin- platelet factor 4 Sepharose columns, antibodies to heparin- platelet factor 4 were purified from the same pool. The effects of heparin, enoxaparin, SR90107A/Org31540, and San Org34006 were evaluated in a platelet aggregation assay using platelet donors (n = 10). At comparable concentrations, hep arin and enoxaparin consistently produced platelet activation, whereas both pentasaccharides failed to produce a response at a concentration up to 100 μg/mL (∼50 μM). Similarly, in the 14C-serotonin release and flow cytometric assays, heparin and enoxaparin produced positive responses (n = 30), whereas the two pentasaccharides consistently failed to produce any effect. These observations suggest that the two pentasaccharides with highly selective anti-Xa activity are devoid of generating anti heparin-platelet factor 4 antibody, do not produce heparin- induced thrombocytopenic responses and may inhibit active heparin-induced thrombocytopenia antibody platelet activation.
doi_str_mv 10.1177/107602969900500410
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Another synthetic pentasaccharide with even more sustained inhibition of factor Xa, SanOrg34006, has also been developed. Both of these agents were tested in comparison to unfraction ated heparin and a low molecular weight heparin (enoxaparin) for their relative platelet activation potential in heparin-induced thrombocytopenia assays. Sera from patients (n = 30) with heparin-induced thrombocytopenia were pooled and validated for heparin-dependent aggregation responses. Using heparin- platelet factor 4 Sepharose columns, antibodies to heparin- platelet factor 4 were purified from the same pool. The effects of heparin, enoxaparin, SR90107A/Org31540, and San Org34006 were evaluated in a platelet aggregation assay using platelet donors (n = 10). At comparable concentrations, hep arin and enoxaparin consistently produced platelet activation, whereas both pentasaccharides failed to produce a response at a concentration up to 100 μg/mL (∼50 μM). Similarly, in the 14C-serotonin release and flow cytometric assays, heparin and enoxaparin produced positive responses (n = 30), whereas the two pentasaccharides consistently failed to produce any effect. 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Another synthetic pentasaccharide with even more sustained inhibition of factor Xa, SanOrg34006, has also been developed. Both of these agents were tested in comparison to unfraction ated heparin and a low molecular weight heparin (enoxaparin) for their relative platelet activation potential in heparin-induced thrombocytopenia assays. Sera from patients (n = 30) with heparin-induced thrombocytopenia were pooled and validated for heparin-dependent aggregation responses. Using heparin- platelet factor 4 Sepharose columns, antibodies to heparin- platelet factor 4 were purified from the same pool. The effects of heparin, enoxaparin, SR90107A/Org31540, and San Org34006 were evaluated in a platelet aggregation assay using platelet donors (n = 10). At comparable concentrations, hep arin and enoxaparin consistently produced platelet activation, whereas both pentasaccharides failed to produce a response at a concentration up to 100 μg/mL (∼50 μM). Similarly, in the 14C-serotonin release and flow cytometric assays, heparin and enoxaparin produced positive responses (n = 30), whereas the two pentasaccharides consistently failed to produce any effect. These observations suggest that the two pentasaccharides with highly selective anti-Xa activity are devoid of generating anti heparin-platelet factor 4 antibody, do not produce heparin- induced thrombocytopenic responses and may inhibit active heparin-induced thrombocytopenia antibody platelet activation.</abstract><cop>Thousand Oaks, CA</cop><pub>SAGE Publications</pub><pmid>10726024</pmid><doi>10.1177/107602969900500410</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record>
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subjects Antibodies - immunology
Anticoagulants
Fibrinolytic Agents - pharmacology
Flow Cytometry
Heparin - immunology
Heparin - pharmacology
Heparin, Low-Molecular-Weight - pharmacology
Humans
Oligosaccharides - pharmacology
Platelet Activation - drug effects
Platelet Factor 4 - immunology
Thrombocytopenia - blood
Thrombocytopenia - chemically induced
title Synthetic Pentasaccharides Do Not Cause Platelet Activation by Antiheparin-Platelet Factor 4 Antibodies
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