DETECTION OF FETAL CELLS IN MATERNAL BLOOD

被引:48
作者
YEOH, SC
SARGENT, IL
REDMAN, CWG
WORDSWORTH, BP
THEIN, SL
机构
[1] UNIV OXFORD,JOHN RADCLIFFE HOSP,NUFFIELD DEPT OBSTET & GYNAECOL,HARRIS BIRTHRIGHT PERINATAL UNIT,OXFORD OX3 9DU,ENGLAND
[2] UNIV OXFORD,JOHN RADCLIFFE HOSP,INST MOLEC MED,MOLEC IMMUNOL UNIT,OXFORD OX3 9DU,ENGLAND
[3] UNIV OXFORD,JOHN RADCLIFFE HOSP,INST MOLEC MED,MOLEC HAEMATOL UNIT,OXFORD OX3 9DU,ENGLAND
基金
英国惠康基金;
关键词
PRENATAL DIAGNOSIS; ENZYMATIC AMPLIFICATION; POLYMERASE CHAIN REACTION; FETAL CELLS; FLOW CYTOMETRY;
D O I
10.1002/pd.1970110207
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
We report the detection of fetal cells in the maternal circulation by enzymatic amplification of a single copy gene sequence that was fetal-specific. Fetal HLA-A2-positive cells were sorted from maternal HLA-A2-negative cells by flow cytometry and confirmed by demonstration of a fetal-specific HLA-DR4 sequence. However, this sequence could not be detected in unenriched maternal DNA prepared at 28 and 32 weeks' gestation. The sensitivity of detection was 1 HLA-DR4-positive cell in 10(5) HLA-DR4-negative cells. We conclude that prenatal diagnosis of paternally inherited autosomal-dominant genetic defects may be possible by selective gene amplification of maternal peripheral blood. However, preliminary enrichment for fetal cells may be necessary.
引用
收藏
页码:117 / 123
页数:7
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