Journal article

Dimeric FcγR ectodomains detect pathogenic anti-platelet factor 4–heparin antibodies in heparin-induced thromobocytopenia

BD Wines, CW Tan, E Duncan, S McRae, RI Baker, RK Andrews, S Esparon, EE Gardiner, PM Hogarth

Journal of Thrombosis and Haemostasis | WILEY | Published : 2018

Abstract

Essentials FcγRIIa mediates life-threatening heparin-induced thrombocytopenia (HIT). Most anti-platelet factor (PF)4-heparin IgGs are not pathogenic so diagnosis of HIT is challenging. Dimeric rsFcγRIIa was used to quantify receptor-binding activity of anti-PF4-heparin antibodies. Dimeric rsFcγRIIa binding specifically correlated with occurrence of HIT. Summary: Background Heparin-induced thrombocytopenia (HIT) is a major and potentially fatal consequence of antibodies produced against platelet factor 4 (PF4)–heparin complexes following heparin exposure. Not all anti-PF4–heparin antibodies are pathogenic, so overdiagnosis can occur, with resulting inappropriate use of alternative anticoagula..

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University of Melbourne Researchers

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Funding Acknowledgements

This work was funded by the National Health and Medical Research Council of Australia and the Victorian Operational Infrastructure Scheme. The authors thank T. Brighton for generously providing the SRA data, J. Jing for expert technical assistance, and A. Chenoweth for reading the manuscript.