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
DOI: 10.1111/jth.14306
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..
View full abstractGrants
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.