Rapid clearance of fetal DNA from maternal plasma

被引:938
作者
Lo, YMD [1 ]
Zhang, J
Leung, TN
Lau, TK
Chang, AMZ
Hjelm, NM
机构
[1] Chinese Univ Hong Kong, Prince Wales Hosp, Dept Chem Pathol, Shatin, New Territories, Peoples R China
[2] Chinese Univ Hong Kong, Prince Wales Hosp, Dept Obstet & Gynecol, Shatin, New Territories, Peoples R China
关键词
D O I
10.1086/302205
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Fetal DNA has been detected in maternal plasma during pregnancy. We investigated the clearance of circulating fetal DNA after delivery, using quantitative PCR analysis of the sex-determining region Y gene as a marker for male fetuses. We analyzed plasma samples from 12 women 1-42 d after delivery of male babies and found that circulating fetal DNA was undetectable by day 1 after delivery. To obtain a higher time-resolution picture of fetal DNA clearance, we performed serial sampling of eight women, which indicated that most women (seven) had undetectable levels of circulating fetal DNA by 2 h postpartum. The mean half-life for circulating fetal DNA was 16.3 min (range 4-30 min). Plasma nucleases were found to account for only part of the clearance of plasma fetal DNA, The rapid turnover of circulating DNA suggests that plasma DNA analysis may be less susceptible to false-positive results, which result from carryover from previous pregnancies, than is the detection of fetal cells in maternal blood; also, rapid turnover may be useful for the monitoring of fete-maternal events with rapid dynamics. These results also may have implications for the study of other types of nonhost DNA in plasma, such as circulating tumor-derived and graft-derived DNA in oncology and transplant patients, respectively.
引用
收藏
页码:218 / 224
页数:7
相关论文
共 34 条
[1]   Identification of fetal DNA and cells in skin lesions from women with systemic sclerosis [J].
Artlett, CM ;
Smith, JB ;
Jimenez, SA .
NEW ENGLAND JOURNAL OF MEDICINE, 1998, 338 (17) :1186-1191
[2]   Fetal DNA in maternal plasma: The plot thickens and the placental barrier thins [J].
Bianchi, DW .
AMERICAN JOURNAL OF HUMAN GENETICS, 1998, 62 (04) :763-764
[3]   Male fetal progenitor cells persist in maternal blood for as long as 27 years postpartum [J].
Bianchi, DW ;
Zickwolf, GK ;
Weil, GJ ;
Sylvester, S ;
DeMaria, MA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (02) :705-708
[4]   ISOLATION OF FETAL DNA FROM NUCLEATED ERYTHROCYTES IN MATERNAL BLOOD [J].
BIANCHI, DW ;
FLINT, AF ;
PIZZIMENTI, MF ;
KNOLL, JHM ;
LATT, SA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1990, 87 (09) :3279-3283
[5]  
Chen XQ, 1996, NAT MED, V2, P1033
[6]   Prenatal diagnosis of sickle cell anaemia and thalassaemia by analysis of fetal cells in maternal blood [J].
Cheung, MC ;
Goldberg, JD ;
Kan, YW .
NATURE GENETICS, 1996, 14 (03) :264-268
[7]  
CHUSED TM, 1972, CLIN EXP IMMUNOL, V12, P465
[8]  
EMLEN W, 1984, CLIN EXP IMMUNOL, V56, P185
[9]   KINETICS AND MECHANISMS FOR REMOVAL OF CIRCULATING SINGLE-STRANDED-DNA IN MICE [J].
EMLEN, W ;
MANNIK, M .
JOURNAL OF EXPERIMENTAL MEDICINE, 1978, 147 (03) :684-699
[10]  
FROST P. G., 1968, CLIN EXP IMMUNOL, V3, P447