FLOW CYTOMETRIC ANALYSIS OF ERYTHROCYTE POPULATIONS IN TN SYNDROME BLOOD USING MONOCLONAL-ANTIBODIES TO GLYCOPHORIN-A AND THE TN-ANTIGEN

被引:20
作者
BIGBEE, WL [1 ]
LANGLOIS, RG [1 ]
STANKER, LH [1 ]
VANDERLAAN, M [1 ]
JENSEN, RH [1 ]
机构
[1] UNIV CALIF LAWRENCE LIVERMORE NATL LAB, DIV SCI, LIVERMORE, CA 94550 USA
来源
CYTOMETRY | 1990年 / 11卷 / 02期
关键词
ELISA; hemagglutination; immunofluorescent labeling; somatic mutation;
D O I
10.1002/cyto.990110207
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Flow cytometric analysis employing monoclonal antibodies to the Tn antigen and glycophorin A was used to characterize the erythrocyte populations present in blood samples from individuals with Tn syndrome. Four monoclonal antibodies specific for the Tn antigen, GalNAc monosaccharide, on human erythrocytes were obtained from a fusion of splenocytes from a Biozzi mouse immunized with red cells from a Tn individual. These monoclonal antibodies specifically recognize GalNAc monosaccharide sites located on the erythrocyte cell surface sialoglycoproteins, glycophorin A and glycophorin B, and do not bind to fixed normal red cells presenting the Neu‐NAcα2‐3Galβ1‐3(NeuNAcα2‐6)GalNAcα1‐O‐Ser(Thr) tetrasaccharide or to fixed neuraminidase‐digested cells presenting the Gal‐GalNAc disaccharide. The percentages of Tn‐positive red cells in samples from six unrelated Tn donors ranged from 28 to 99%. Binding of the glycophorin A‐specific monoclonal antibodies showed that the erythrocytes composing the Tn‐negative fraction presented normal amounts of the M and N epitopes on glycophorin A. The presumed somatic mutational origin of Tn‐positive cells was tested in blood samples from five normal donors; three possible Tn cells were observed after analysis of a total of 1.1 X 107 erythrocytes, suggesting that the frequency of such cells in normal individuals is > 1 X 10−6. Copyright © 1990 Wiley‐Liss, Inc.
引用
收藏
页码:261 / 271
页数:11
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