Mepacrine flow cytometry assay for the diagnosis of platelet δ-granule defects : literature review on methods - towards a shared detailed protocol.


Journal

Thrombosis and haemostasis
ISSN: 2567-689X
Titre abrégé: Thromb Haemost
Pays: Germany
ID NLM: 7608063

Informations de publication

Date de publication:
11 Sep 2024
Historique:
medline: 12 9 2024
pubmed: 12 9 2024
entrez: 11 9 2024
Statut: aheadofprint

Résumé

Accurate assessment of platelet secretion is essential for the diagnosis of inherited or acquired platelet function disorders (PFDs) and more specifically in identifying δ-storage pool disease. Mepacrine, a fluorescent dye, specifically accumulates in platelet δ-granules. The mepacrine flow cytometry (FCM) assay has been used for more than half a century in the clinical laboratory as a diagnostic tool for platelet δ-granule disorders. The assay requires a small volume of blood, can be performed in thrombocytopenic patients, provides rapid assessment of δ-granule content and secretion and, thus, enables differentiation between storage and release defects. FCM has been shown to have added value compared to light transmission aggregometry. There is however a broad heterogeneity in methods, reagents, and equipment used. Lack of standardization and limited data on analytical and clinical performances have led the 2022 ISTH SSC Subcommittee on Platelet Physiology expert consensus to rate this assay as simple but of uncertain value. Yet, the data used by experts to formulate the recommendations were not discussed and even not mentioned. Guidance for laboratory studies of platelet secretion assay would be very helpful for clinical laboratories and health authorities especially considering the implications of the new In Vitro Diagnostic Regulation (IVDR) in Europe. The purpose of the present work was to systematically review the reported methodologies for the mepacrine FCM assay and to offer an example of detailed protocol. This would help standardization and pave the way for more rigorous comparative studies.

Identifiants

pubmed: 39260401
doi: 10.1055/a-2413-2870
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

Thieme. All rights reserved.

Déclaration de conflit d'intérêts

The authors declare that they have no conflict of interest.

Auteurs

Mehdi Khourssaji (M)

Hematology Laboratory, Université catholique de Louvain, CHU UCL Namur, Namur Thrombosis and Hemostasis Center (NTHC), Namur Research Institute for Life Sciences (NARILIS), Yvoir, Belgium.

Marion Bareille (M)

Hematology Laboratory, Université catholique de Louvain, CHU UCL Namur, Namur Thrombosis and Hemostasis Center (NTHC), Namur Research Institute for Life Sciences (NARILIS), Yvoir, Belgium.

Lorenzo Alberio (L)

Division of Haematology and Central Haematology Laboratory, CHUV, Lausanne, Switzerland.

Delphine Borgel (D)

Laboratoire d'Hématologie, AP-HP, Hôpital Necker-Enfants malades, Paris, France., Paris, France.

Marc Fouassier (M)

Centre de Traitement de l'Hémophilie, CHU Hôtel-Dieu, NANTES, France.

Marie Christine Bene (MC)

Laboratoire d'hématologie, CHU Hôtel-Dieu, NANTES, France.

Thomas Lecompte (T)

Angiology Division, Université de Lorraine CHRU Nancy, Nantes, France.

François Mullier (F)

Hematology Laboratory, Université catholique de Louvain, CHU UCL Namur, Namur Thrombosis and Hemostasis Center (NTHC), Namur Research Institute for Life Sciences (NARILIS), Yvoir, Belgium.
Université catholique de Louvain, Institut de Recherche Expérimentale et Clinique (IREC) - Pôle Mont, Namur, Belgium.

Classifications MeSH