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Detection of granulocyte-reactive antibodies: a comparison of different methods
被引:17
|作者:
Heinzl, M. W.
[1
]
Schoenbacher, M.
[1
]
Dauber, E-M
[1
]
Panzer, S.
[1
]
Mayr, W. R.
[1
]
Koermoeczi, G. F.
[1
]
机构:
[1] Med Univ Vienna, Dept Blood Grp Serol & Transfus Med, A-1090 Vienna, Austria
关键词:
flow cytometry;
granulocyte immunology;
granulocyte-reactive antibodies;
human neutrophil antigens;
microbeads assay;
ACUTE LUNG INJURY;
TRANSFUSION REACTIONS;
LEUKOCYTE ANTIBODIES;
BLOOD-DONORS;
ANTIGEN;
ALLOANTIBODIES;
D O I:
10.1111/vox.12227
中图分类号:
R5 [内科学];
学科分类号:
1002 ;
100201 ;
摘要:
Background and ObjectivesGranulocyte-reactive antibodies can cause autoimmune and neonatal immune neutropenias as well as transfusion-related acute lung injury. The classical antibody-detection methods granulocyte aggregation test (GAT), granulocyte immunofluorescence test (GIFT) and monoclonal antibody-specific immobilization of granulocyte antigens (MAIGA) are time-consuming and technically challenging. In recent years, flow cytometric white blood cell immunofluorescence test (Flow-WIFT) and the microbeads assay LabScreen (R) Multi have emerged and are still subject of evaluation. These serological tests were compared on a screening and specification level. Materials and MethodsFor screening, the combination of GAT/GIFT was compared to Flow-WIFT testing 333 samples. Positive samples were further analysed with MAIGA and LabScreen (R) Multi. ResultsGranulocyte aggregation test/GIFT detected 77 positive samples, Flow-WIFT found 108 granulocyte-reactive samples. Six Samples were only positive in GAT/GIFT, and 37 samples were only positive in Flow-WIFT (=0682). Antibody specification with MAIGA and the microbeads assay confirmed granulocyte-reactivity in 83 cases with 70 matching results (=0742). However, out of six detected human neutrophil antigen (HNA) reactivities only two specificities matched in both assays. ConclusionFlow-WIFT may be a valuable addition to GIFT for granulocyte-reactive antibody screening. MAIGA remains the most reliable laboratory method for antibody specification.
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页码:287 / 293
页数:7
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