HLA antibody identification with single antigen beads compared to conventional methods

被引:89
作者
El-Awar, N [1 ]
Lee, J [1 ]
Terasaki, PI [1 ]
机构
[1] One Lambda Inc, Res 2, Los Angeles, CA 90064 USA
关键词
single antigen beads; monoclonal antibodies; UCLA serum exchange; flow cytometry; antibody specificity;
D O I
10.1016/j.humimm.2005.07.005
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Single antigen (SA) beads coated with Class I HLA antigens from recombinant cells lines were tested with 170 mouse monoclonal antibodies (mAbs). The HLA specificities of all mAbs were previously determined by the cytotoxicity assay (CDC). There were 100 mAbs which produced the expected reactions with the SA beads, indicating that the SA beads coated with the antigens had reacted properly. Sixty one mAbs were positive with one or more antigen(s) that shared unique amino acids (aa) possibly constituting a common epitope. Single antigen beads were then tested on 58 alloantisera analyzed by 63 laboratories of the UCLA serum exchange (UCLA-SE). Many specificities detected by the single antigen beads were missed by the laboratories employing conventional methods. Most of the missed specificities were of lower frequency, although in some instances, even common specificities were missed. These findings have important implications regarding the use of specificities to predict positive crossmatch, to selecting platelet donors for highly sensitized recipients, and analysis of sera for donor specific antibodies. Human Immunology 66, 989-997 (2005). (c) American Society for Histocompatibility and Immunogenetics, 2005. Published by Elsevier Inc.
引用
收藏
页码:989 / 997
页数:9
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