Since platelets express both platelet-specific and class I HLA antigens, serum antiplatelet reactivity assessed by most platelet antibody techniques could be due to antibodies with either or both specificities. Flow cytometric analysis of sera for detection of antiplatelet antibody commonly employs
Flow cytometry analysis of platelet antibodies
β Scribed by Dr. Paul R. Finley; R. Jane Williams; Carla Fletcher
- Publisher
- John Wiley and Sons
- Year
- 1988
- Tongue
- English
- Weight
- 708 KB
- Volume
- 2
- Category
- Article
- ISSN
- 0887-8013
No coin nor oath required. For personal study only.
β¦ Synopsis
We have devised assays to detect both circulating alloantibodies to platelets (indirect assay) and platelet-association IgG and IgM (direct assay) using a flow cytometric technique. A variety of patients with immune thrombocytopenia were studied. Employment of a confocal lens in the flow cytometer increased the discrimination power of the instrument. Patients with autoimmune thrombocytopenia (idiopathic thrombocytic purpura [ITP], systemic Iupus erythematosus (SLE), lymphoma, leukemia, and drug-induced thrombocytope-nia showed asignificant increase in plateletassociated antibody. Circulating antibodies to platelets (alloantibodies) were demonstrated in cases of platelet refractoriness and neonatal isoimmune purpura. Day-today precision of the assays ranged from 3% to 6% (coefficient of variation). No interference was shown in the presence of hemoglobin (5 glL), triglycerides (10 glL), or polyclonal and monoclonal immunoglobulinemia (50 glL: IgG, IgA, IgM). The sensitivity of the direct assay was 500 attograrns of IgG or IgM platelet.
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