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Multicentre evaluation of 5B9, a monoclonal anti-PF4/heparin IgG mimicking human HIT antibodies, as an internal quality control in HIT functional assays: Communication from the ISTH SSC Subcommittee on Platelet Immunology.
Pouplard, Claire; Rollin, Jérôme; Vayne, Caroline; Charuel, Noémie; Ahmadi, Zohra; Alberio, Lorenzo; Azjenberg, Nadine; Althaus, Karina; Bakchoul, Tamam; Chong, Beng; Curtis, Brian R; Faille, Dorothée; Gomez, Francisco-Javier; Gresele, Paolo; Morel-Kopp, Marie-Christine; Mullier, François; Nazy, Izhac; Smith, James W; Greinacher, Andreas; Gruel, Yves.
Afiliación
  • Pouplard C; University of Tours, EA7501 GICC, CHRU de Tours, Department of Haemostasis, Tours, France.
  • Rollin J; University of Tours, EA7501 GICC, CHRU de Tours, Department of Haemostasis, Tours, France.
  • Vayne C; University of Tours, EA7501 GICC, CHRU de Tours, Department of Haemostasis, Tours, France.
  • Charuel N; University of Tours, EA7501 GICC, CHRU de Tours, Department of Haemostasis, Tours, France.
  • Ahmadi Z; Haematology Research Unit, St George and Sutherland Clinical School, University of New South Wales, Sydney, NSW, Australia.
  • Alberio L; Service and Central Laboratory of Hematology, Lausanne University Hospital (CHUV) and University of Lausanne, Lausanne, Switzerland.
  • Azjenberg N; University of Paris, INSERM U1148 LVTS, Department of Hematology, AP-HP, Bichat-Claude Bernard Hospital, Paris, France.
  • Althaus K; Transfusion Medicine, Medical Faculty of Tubingen, University of Tubingen, Tubingen, Germany.
  • Bakchoul T; Transfusion Medicine, Medical Faculty of Tubingen, University of Tubingen, Tubingen, Germany.
  • Chong B; Haematology Research Unit, St George and Sutherland Clinical School, University of New South Wales, Sydney, NSW, Australia.
  • Curtis BR; Blood Research Institute, Versiti, Blood Center of Wisconsin, Milwaukee, Wisconsin, USA.
  • Faille D; University of Paris, INSERM U1148 LVTS, Department of Hematology, AP-HP, Bichat-Claude Bernard Hospital, Paris, France.
  • Gomez FJ; Service and Central Laboratory of Hematology, Lausanne University Hospital (CHUV) and University of Lausanne, Lausanne, Switzerland.
  • Gresele P; Department of Medicine and Surgery, Section of Internal and Cardiovascular Medicine, University of Perugia, Perugia, Italy.
  • Morel-Kopp MC; Department of Haematology and Transfusion Medicine, Royal North Shore Hospital, and Northern Blood Research Centre, Kolling Institute, The University of Sydney, Sydney, NSW, Australia.
  • Mullier F; Université catholique de Louvain, CHU UCL Namur, Namur Thrombosis and Hemostasis Center (NTHC), Hematology Laboratory, Namur Research for Life Sciences, Yvoir, Belgium.
  • Nazy I; Department of Medicine, Michael G. DeGroote School of Medicine, McMaster University, Hamilton, ON, Canada.
  • Smith JW; McMaster Centre for Transfusion Research, Hamilton, ON, Canada.
  • Greinacher A; Department of Medicine, Michael G. DeGroote School of Medicine, McMaster University, Hamilton, ON, Canada.
  • Gruel Y; Institut fuer Immunologie und Transfusionsmedizin, Universitaetsmedizin Greifswald, Greifswald, Germany.
J Thromb Haemost ; 20(1): 252-259, 2022 01.
Article en En | MEDLINE | ID: mdl-34657390
BACKGROUND: Functional tests for the diagnosis of heparin-induced thrombocytopenia (HIT) exhibit variable performance. OBJECTIVES: We evaluated in a multicenter study whether 5B9, a monoclonal anti-PF4/heparin IgG mimicking human HIT antibodies, could be used as an internal quality control. METHODS: 5B9 was sent to 11 laboratories in seven countries, and six initial concentrations ranging from 10 to 400 µg/mL were tested by heparin-induced platelet activation assay (HIPA), serotonin release assay (SRA), platelet aggregation test (PAT), flow cytometry (FC), or heparin-induced multiple-electrode aggregometry (HIMEA). Each method was evaluated in three different laboratories using experimental procedures identical to those usually applied for the diagnosis of HIT by testing platelets from 10 different healthy donors. RESULTS: The procedures used varied among the laboratories, particularly when platelet-rich plasma and whole blood were used. Nevertheless, positive results were obtained with at least 100 µg/ml of 5B9 for most donors tested by all centers (except one) performing HIPA, SRA, or HIMEA. FC and PAT results were more heterogeneous. FC results from one center that used washed platelets preincubated with PF4 were positive with all donors at 50 µg/ml 5B9, but at least 200 µg/ml of 5B9 were required to activate cells with most donors tested using PAT. CONCLUSION: This study confirms that HIT functional tests are not well standardized and exhibit variable sensitivity for the detection of platelet-activating antibodies. However, 5B9 is a potentially useful tool to standardize functional tests, to select responding platelet donors, and consequently to improve the performance of these assays and comparability between laboratories.
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Texto completo: 1 Base de datos: MEDLINE Asunto principal: Trombocitopenia / Factor Plaquetario 4 Tipo de estudio: Clinical_trials / Diagnostic_studies Límite: Humans Idioma: En Revista: J Thromb Haemost Asunto de la revista: HEMATOLOGIA Año: 2022 Tipo del documento: Article País de afiliación: Francia

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Trombocitopenia / Factor Plaquetario 4 Tipo de estudio: Clinical_trials / Diagnostic_studies Límite: Humans Idioma: En Revista: J Thromb Haemost Asunto de la revista: HEMATOLOGIA Año: 2022 Tipo del documento: Article País de afiliación: Francia