A review of platelet secretion assays for the diagnosis of inherited platelet secretion disorders

被引:78
作者
Mumford, Andrew D. [1 ]
Frelinger, Andrew L., III [2 ]
Gachet, Christian [3 ]
Gresele, Paolo [4 ]
Noris, Patrizia [5 ]
Harrison, Paul [6 ]
Mezzano, Diego [7 ,8 ]
机构
[1] Univ Bristol, Sch Clin Sci, Bristol, Avon, England
[2] Harvard Univ, Sch Med, Dana Farber Canc Inst, Ctr Platelet Res Studies,Div Hematol Oncol,Boston, Boston, MA 02115 USA
[3] Univ Strasbourg, UMR INSERM S949, Etab Francais Sang Alsace, Strasbourg, France
[4] Univ Perugia, Dept Med, I-06100 Perugia, Italy
[5] Univ Pavia, IRCCS Policlin San Matteo Fdn, Dept Internal Med, I-27100 Pavia, Italy
[6] Univ Birmingham, Sch Med, Sch Immun & Infect, Birmingham, W Midlands, England
[7] Pontificia Univ Catolica Chile, Sch Med, Santiago, Chile
[8] Conicyt 1130853, Budapest, Hungary
关键词
Platelet pathology; inherited; acquired; secretion; exocytosis; diagnosis management; STORAGE POOL-DEFICIENCY; PERFORMANCE LIQUID-CHROMATOGRAPHY; LIGHT TRANSMISSION AGGREGOMETRY; ADENOSINE-TRIPHOSPHATE RELEASE; LINKED-IMMUNOSORBENT-ASSAY; ALPHA-GRANULE PROTEINS; FACTOR-V; BETA-THROMBOGLOBULIN; WHOLE-BLOOD; P-SELECTIN;
D O I
10.1160/TH14-11-0999
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Measurement of platelet granule release to detect inherited platelet secretion disorders (IPSDs) is essential for the evaluation of patients, with abnormal bleeding and is necessary to distinguish which granule sub-types are affected and whether there is abnormal granule biosynthesis or secretion. The radioactive serotonin incorporation and release assay, described before 1970, is still considered the "gold standard" test to assess platelet delta-granule release, although is unsuitable, for clinical diagnostic laboratories. Luciferin-based assays, such as lumiaggregometry, are the most widely performed alternatives, although these methods do not distinguish defects in delta-granule biosynthesis from defects in secretion. Platelet alpha-granule release is commonly evaluated using flow cytometry by measuring surface exposure of P-selectin after platelet activation. However, this assay has poor sensitivity for some a-granule disorders. Only few studies have been published with more recently developed assays and no critical reviews on these methods are available. In this review, we describe the rationale for developing robust and accurate laboratory tests of platelet granule release and describe the characteristics of the currently available tests. We identify an unmet need for further systematic evaluation of new assays and for standardisation of methodologies for clinical diagnostic laboratories.
引用
收藏
页码:14 / 25
页数:12
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