Flow cytometric HLA-B27 screening: Cross-reactivity patterns of commercially available anti-HLA-B27 monoclonal antibodies with other HLA-B antigens

被引:33
作者
Levering, WHBM
Wind, H
Sintnicolaas, K
Hooijkaas, H
Gratama, JW
机构
[1] Sanquin Blood Bank SW Reg, Lab Histocompatibil & Immunogenet, NL-3001 KJ Rotterdam, Netherlands
[2] Erasmus MC, Dept Immunol, Rotterdam, Netherlands
[3] Erasmus MC, Dept Internal Oncol, Rotterdam, Netherlands
来源
CYTOMETRY PART B-CLINICAL CYTOMETRY | 2003年 / 54B卷 / 01期
关键词
HLA-B27; cross-reactivity; monoclonal antibody; flow cytometry; molecules of equivalent soluble fluorochrome units;
D O I
10.1002/cyto.b.10022
中图分类号
R446 [实验室诊断]; R-33 [实验医学、医学实验];
学科分类号
1001 ;
摘要
Background: Some 50 clinical laboratories in the Benelux perform flow cytometric HLA-B27 screening and participate in the Benelux external quality assessment scheme operational since 1995. Results from this scheme indicate that cross-reactivity of HLA-B27 monoclonal antibodies (mAbs) is a major problem. Methods: We analyzed cross-reactivity patterns of commercially available mAbs for HLA-B27 screening. Three clones of HLA-B27 mAb (ABC-m3, n = 3; FD705; and GS145.2) from five manufacturers were evaluated. Test cells were selected as to express HLA-B antigens with known serologic cross-reactions (HLA-B7, B12, B13, B16, B17, B22, B37, B40, B41, B42, B47, and B48). Cells without B27 cross-reactive antigens (B5, B8, B14, B15, B21, and B35) and cells positive for B27 were included as controls. All tests were performed and interpreted as recommended by the manufacturers. Cross-reactivity was defined as increased fluorescence intensity in comparison with the baseline reactivity observed with the corresponding immunoglobulin G isotype control mAb. Results and Conclusions: All mAbs tested showed cross-reactivity, ranging from weak (+/-) to strong (+), with different antigens and different degrees of intensity-ABC-m3: (+/-) B12, B16, B17, B41, B47, and B48 and (+) B7, B13, B22, B37, B40, and B42; GS145.2: (+/-) B13, B17, B22, B40, and B47 and (+) B7, B16, B37, B42, and B48; FD705: (+/-) B12, B13, B16, and B48 and (+) B17, B37, and B47. If one mAb had been used for HLA-B27 screening, ABC-m3 would have yielded nine false-positive B27 assignments, FD705 would have yielded seven, and GS145.2 would have yielded two. This problem largely canbe avoided by the combined use of two different mAb clones. The combination of FD705 and GS145.2 yielded the best results, with one false-positive HLA-B27 assignment among the 99 HLA-B27(-) samples of this highly selected panel. (C) 2003 Wiley-Liss, Inc.
引用
收藏
页码:28 / 38
页数:11
相关论文
共 36 条
[1]  
ALBRECHT J, 1987, CLIN CHEM, V33, P1619
[2]  
*AM SOC HIST IMM, 1998, STAND HIST TEST
[3]   HLA-B27-associated cardiac disease [J].
Bergfeldt, L .
ANNALS OF INTERNAL MEDICINE, 1997, 127 (08) :621-629
[4]  
BREWERTON DA, 1973, LANCET, V1, P904
[5]  
Chen JC, 2002, CYTOMETRY, V50, P280
[6]  
Chen JC, 1996, CYTOMETRY, V26, P286
[7]   The detection of the HLA-B27 antigen by immunomagnetic separation and enzyme-linked immunosorbent assay - comparison with a flow cytometric procedure [J].
Chou, CT ;
Tsai, YF ;
Liu, JA ;
Wei, JCC ;
Liao, TS ;
Chen, ML ;
Liu, LY .
JOURNAL OF IMMUNOLOGICAL METHODS, 2001, 255 (1-2) :15-22
[8]   Routine HLA-B27 typing by flow cytometry: differentiation of the products of HLA-B*2702, B*2705 and B*2708 [J].
Coates, E ;
Darke, C .
EUROPEAN JOURNAL OF IMMUNOGENETICS, 1998, 25 (01) :29-37
[9]  
DOMINGUEZ O, 1992, IMMUNOGENETICS, V36, P277
[10]  
*EFI, 2000, STAND HIST TEST