alexa A Flow Cytometric Assay For The Confirmation Of Heparin-induced Thrombocytopenia (HIT) | 64874
ISSN: 2155-9864

Journal of Blood Disorders & Transfusion
Open Access

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7th World Hematologists Congress
May 08-09, 2017 Barcelona, Spain

Elvira Malicev
Blood Transfusion Centre of Slovenia, Slovenia
ScientificTracks Abstracts: J Blood Disord Transfus
DOI: 10.4172/2155-9864-C1-022
Abstract
Heparin-induced thrombocytopenia (HIT) is induced by the antibodies against neoepitopes in complexes of heparin with a platelet factor 4 (PF4). Anti-heparin/PF4 antibodies are capable of platelet activation by cross-linking to platelet Fcγ receptor IIa. Patients with HIT usually have thrombocytopenia between 5-10 days after heparin therapy has started and are at an increased risk of developing venous or/and arterial thromboses. However, not all patients with detected anti-heparin/PF4 antibodies go on to develop HIT. The diagnosis is a challenge and requires an exact analysis of the clinical and laboratory parameters. Laboratory testing includes both serological and functional assays. Enzyme immunoassays (ELISA) are most often used for detecting the presence or absence of anti-heparin/PF4 antibodies in a patient`s serum. ELISA is highly sensitive but has a low specificity because it detects both platelet activating and platelet non-activating anti-heparin/PF4 antibodies. To confirm the presence of pathogenic platelet activating antibodies, one of the functional assays has to be done. Functional assays generally require technical expertise, special equipment and the use of fresh donor platelets; therefore, laboratories rarely perform them. The serotonin release assay (SRA) and the heparininduced platelet activation assay (HIPA) are the most well-known functional assays. Another possibility to confirm HIT could be the use of flow cytometry. We have introduced the functional flow cytometric assay for routine testing of suspect HIT patients. The assay is based on detection of CD61 antigens, and CD62P molecules (P-selectins), expressed on platelet surface after α-granule exocytosis. Each sample (patient’s serum, positive and negative control) is tested against fresh platelets obtained from four healthy donors. The assay is positive when at least two of four donor platelets are activated at a low concentration of heparin, and at the same time the parallel reaction is inhibited in the presence of excess heparin.
Biography

Elvira Maličev is an Assistant Professor at University of Ljubljana and Head of Laboratory for flow cytometry at Blood Transfusion Centre of Slovenia, where she works on Platelets, Erythrocytes and Stem cells. Her main research interests include Mesenchymal and Hematopoietic Stem Cell Biology.

Email: [email protected]

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