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  3. Variable impairment of platelet functions in patients with severe, genetically linked immune deficiencies.

Variable impairment of platelet functions in patients with severe, genetically linked immune deficiencies.

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DOI
10.7892/boris.110088
Publisher DOI
10.3324/haematol.2017.176974
PubMed ID
29242293
Abstract
In patients with dysfunctions of the Ca2+ channel ORAI1, stromal interaction molecule 1 (STIM1) or integrin-regulating kindlin-3 (FERMT3), severe immunodeficiency is frequently linked to abnormal platelet activity. In this paper, we studied in nine rare patients, including relatives, with confirmed genetic mutations of ORAI1, STIM1 or FERMT3, platelet responsiveness by multi-parameter assessment of whole blood thrombus formation under high-shear flow conditions. In platelets isolated from 5 out of 6 patients with ORAI1 or STIM1 mutations, store-operated Ca2+ entry (SOCE) was (in)completely defective compared to control platelets. Parameters of platelet adhesion and aggregation on collagen microspots were impaired for 4/6 patients, in part related to a low platelet count. For 4 patients, platelet adhesion/aggregation and procoagulant activity on VWF/rhodocytin and VWF/fibrinogen microspots were impaired, independently of platelet count and partly correlated with SOCE deficiency. Measurement of thrombus formation at low shear rate confirmed a larger impairment of platelet functionality in the ORAI1 patients than in the STIM1 patient. For 3 patients/relatives with a FERMT3 mutation, all parameters of thrombus formation were strongly reduced regardless of the microspot. Bone marrow transplantation, required by two patients, resulted in overall improvement of platelet function. We concluded that multiparameter assessment of whole-blood thrombus formation, in a surface-dependent way, can detect: (i) additive effects of low platelet count and impaired platelet functionality; (ii) aberrant ORAI1-mediated Ca2+ entry; (iii) differences in platelet activation between patients carrying the same ORAI1 mutation; (iv) severe platelet function impairment linked to a FERMT3 mutation and bleeding history.
Date Issued
2018-03
Publication Type
Article
Subject(s)
600 Technology > 610 Medicine & health
Subjects
FERMT3 ORAI1 Platelets STIM1 Store-operated calcium entry (SOCE)
Language(s)
en
Author(s)
Nagy, Magdolna
Mastenbroek, Tom G
Mattheij, Nadine J A
de Witt, Susanne
Clemetson, Kenneth John  
Department for BioMedical Research, Forschungsgruppe Hämatologie (Erwachsene)  
Universitätsklinik für Hämatologie und Hämatologisches Zentrallabor  
Kirschner, Janbernd
Schulz, Ansgar S
Vraetz, Thomas
Speckmann, Carsten
Braun, Attila
Cosemans, Judith M E M
Zieger, Barbara
Heemskerk, Johan W M
Additional Credits
Universitätsklinik für Hämatologie und Hämatologisches Zentrallabor  
Department for BioMedical Research, Forschungsgruppe Hämatologie (Erwachsene)  
Journal
Haematologica - the hematology journal
Publisher
Ferrata-Storti Foundation
ISSN
0390-6078
Access(Rights)
Unknown
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