Search for the optimal fetal cell antibody: Results of immunophenotyping studies using flow cytometry

被引:39
作者
Zheng, YL
Zhen, DK
DeMaria, MA
Berry, SM
Wapner, RJ
Evans, MI
Copeland, D
Williams, JM
Bianchi, DW
机构
[1] TUFTS UNIV NEW ENGLAND MED CTR,DEPT PEDIAT,BOSTON,MA 02111
[2] TUFTS UNIV,SCH MED,NEW ENGLAND MED CTR HOSP,DEPT OBSTET & GYNECOL,BOSTON,MA 02111
[3] WAYNE STATE UNIV,HUTZEL HOSP,DEPT OBSTET & GYNECOL,DETROIT,MI 48201
[4] WAYNE STATE UNIV,SCH MED,DETROIT,MI 48201
[5] WAYNE STATE UNIV,HUTZEL HOSP,DEPT PATHOL,CTR MOL MED & GENET,DETROIT,MI 48201
[6] THOMAS JEFFERSON UNIV,MED COLL & HOSP,DEPT OBSTET & GYNECOL,PHILADELPHIA,PA 19107
[7] GENZYME CORP,CAMBRIDGE,MA 02139
关键词
D O I
10.1007/s004390050462
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Fetal nucleated cells circulating in maternal peripheral blood are a noninvasive source of fetal DNA for prenatal genetic diagnoses. The successful isolation of fetal cells from maternal blood depends upon identification of differences between fetal and maternal cell surface antigen expression. To our best knowledge, a monoclonal antibody that binds only fetal blood cells has not yet been identified. We studied antigens recognized by six different monoclonal antibodies for their biologic expression on fetal blood cells as a function of gestational age, and compared their ability to bind fetal but not maternal cells. The results suggest a relationship between gestational age and nucleated cell surface antigen expression. The monoclonal antibodies FB3-2, H3-3, CD71 and 2-6B/6 are suitable reagents for first or early second trimester fetal cell isolation, although FB3-2 and H3-3 are more specific for fetal cells due to significantly lower expression of these antigens on maternal mononuclear cells. The observation that samples from fetuses with chromosome abnormalities or multiple structural anomalies express higher levels of these antigens indicates that these reagents will potentiate the detection of abnormal fetal cells in maternal blood samples.
引用
收藏
页码:35 / 42
页数:8
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